U.S. flag

An official website of the United States government

Baylor Genetics

General information

Baylor Genetics

2450 Holcombe, Grand Blvd. - Sample Receiving Dock
Houston
Texas
United States - 77021-2024
https://www.baylorgenetics.com/
Organization ID: 1006

Personnel

View this laboratory in GTR

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 41938

Gene

GeneSubmissionsLast Updated
AAAS1Feb 21, 2021
AAGAB1Feb 21, 2021
AARS17Oct 2, 2023
AARS214Oct 2, 2023
AASS1Feb 21, 2021
ABAT11Dec 7, 2023
ABCA110Oct 2, 2023
ABCA21Feb 19, 2023
ABCA34Mar 5, 2021
ABCA46Mar 5, 2021
ABCB12Mar 5, 2021
ABCB11100Dec 7, 2023
ABCB412Oct 2, 2023
ABCB71Oct 2, 2023
ABCC25Feb 21, 2021
ABCC610Oct 2, 2023
ABCC8154Dec 7, 2023
ABCC95Oct 2, 2023
ABCD127Dec 7, 2023
ABCD41Feb 19, 2023
ABCG52Feb 21, 2021
ABCG82Mar 5, 2021
ABHD122Mar 5, 2021
ABHD14A-ACY16Mar 5, 2021
ABHD16A1Dec 14, 2023
ABL18Feb 19, 2023
ABRAXAS11Dec 7, 2023
ACACA1Feb 21, 2021
ACAD111Feb 21, 2021
ACAD87Mar 12, 2023
ACAD981Dec 7, 2023
ACADM137Dec 14, 2023
ACADS3Feb 19, 2023
ACADSB7Mar 12, 2023
ACADVL174Dec 14, 2023
ACAN5Mar 5, 2021
ACAT163Dec 7, 2023
ACD1Mar 5, 2021
ACE3Mar 5, 2021
ACER31Feb 21, 2021
ACO28Oct 2, 2023
ACOX122Dec 7, 2023
ACOX21Mar 5, 2021
ACP53Mar 5, 2021
ACSF3100Dec 7, 2023
ACSL42Oct 2, 2023
ACTA112Mar 12, 2023
ACTA23Feb 19, 2023
ACTA2-AS11Feb 19, 2023
ACTB17Mar 12, 2023
ACTC18Feb 19, 2023
ACTG14Mar 5, 2021
ACTG23Feb 19, 2023
ACTL6A5Jul 1, 2021
ACTL6B5Feb 19, 2023
ACTN12Feb 19, 2023
ACTN23Feb 21, 2021
ACTN42Mar 5, 2021
ACVR11Mar 14, 2019
ACVR2B2Feb 19, 2023
ACVRL14Oct 2, 2023
ACY16Mar 5, 2021
ADA70Dec 7, 2023
ADA28Feb 19, 2023
ADAM172Mar 5, 2021
ADAMTS102Mar 5, 2021
ADAMTS136Mar 12, 2023
ADAMTS171Mar 5, 2021
ADAMTS27Mar 5, 2021
ADAMTSL41Feb 19, 2023
ADAMTSL4-AS21Feb 19, 2023
ADAR7Oct 2, 2023
ADAT37Mar 5, 2021
ADCY11Feb 21, 2021
ADCY56Dec 14, 2023
ADD33Feb 21, 2021
ADGRG13Mar 5, 2021
ADGRG21Feb 21, 2021
ADGRG61Feb 21, 2021
ADGRL11Dec 14, 2023
ADGRL1-AS11Dec 14, 2023
ADGRV113Dec 14, 2023
ADK1Feb 21, 2021
ADNP6Mar 5, 2021
ADNP-AS12Feb 21, 2021
ADPRS3Feb 21, 2021
ADRA2B3Mar 5, 2021
ADSL9Oct 2, 2023
ADSS12Feb 19, 2023
AEBP13Mar 5, 2021
AFF27Feb 19, 2023
AFF32Oct 2, 2023
AFF43Mar 5, 2021
AFG2A8Feb 19, 2023
AFG3L24Mar 5, 2021
AGA41Dec 7, 2023
AGA-DT2Dec 7, 2023
AGK4Mar 5, 2021
AGL150Dec 7, 2023
AGPAT22Nov 14, 2016
AGPS16Dec 7, 2023
AGRN16Oct 2, 2023
AGTPBP13Feb 21, 2021
AGXT71Dec 7, 2023
AHDC114Oct 2, 2023
AHI15Feb 19, 2023
AHSG2Mar 5, 2021
AIFM15Dec 7, 2023
AIMP11Oct 2, 2023
AIMP21Feb 19, 2023
AIP43Dec 7, 2023
AIRE2Mar 5, 2021
AK24Mar 5, 2021
AKAP97Feb 19, 2023
AKR1D13Feb 21, 2021
AKT11Mar 5, 2021
AKT21Mar 5, 2021
ALAD1Mar 5, 2021
ALB1Feb 19, 2023
ALDH18A18Mar 12, 2023
ALDH3A27Oct 2, 2023
ALDH4A13Mar 5, 2021
ALDH5A14Feb 19, 2023
ALDH6A11Mar 5, 2021
ALDH7A15Mar 5, 2021
ALDOB35Dec 7, 2023
ALG15Oct 2, 2023
ALG113Mar 5, 2021
ALG123Feb 21, 2021
ALG135Feb 19, 2023
ALG23Mar 5, 2021
ALG35Feb 19, 2023
ALG653Dec 7, 2023
ALG87Oct 2, 2023
ALG95Feb 19, 2023
ALK208Dec 7, 2023
ALKBH81Feb 19, 2023
ALMS117Feb 19, 2023
ALOX12B7Mar 12, 2023
ALOXE32Oct 2, 2023
ALPK11Feb 19, 2023
ALPK37Oct 2, 2023
ALPL141Dec 7, 2023
ALS25Feb 19, 2023
ALX41Mar 5, 2021
AMACR1Feb 21, 2021
AMER15Dec 14, 2023
AMMECR11Oct 2, 2023
AMN1Mar 5, 2021
AMPD13Mar 5, 2021
AMPD25Feb 19, 2023
AMT40Dec 7, 2023
ANAPC71Feb 19, 2023
ANK14Oct 2, 2023
ANK25Mar 5, 2021
ANK312Oct 2, 2023
ANKLE22Feb 21, 2021
ANKRD1148Oct 2, 2023
ANKRD171Feb 19, 2023
ANKRD265Dec 7, 2023
ANKS63Mar 5, 2021
ANLN2Feb 19, 2023
ANO103Mar 5, 2021
ANO56Oct 2, 2023
ANOS12Feb 21, 2021
ANTXR11Mar 5, 2021
ANTXR25Mar 5, 2021
AOPEP51Dec 7, 2023
AP2S11Feb 21, 2021
AP3B119Dec 7, 2023
AP3B27Mar 5, 2021
AP4B16Mar 5, 2021
AP4B1-AS15Mar 5, 2021
AP4E14Oct 2, 2023
AP4M110Feb 19, 2023
AP4S12Mar 5, 2021
AP5Z114Oct 2, 2023
APBB12Sep 27, 2019
APC652Dec 7, 2023
APC28Feb 19, 2023
APOA52Feb 19, 2023
APOB12Oct 2, 2023
APOL11Mar 5, 2021
APP1Feb 21, 2021
APTX2Mar 5, 2021
AQP23Feb 21, 2021
AQP5-AS11Feb 21, 2021
AR4Oct 2, 2023
ARCN12Mar 5, 2021
ARF11Feb 19, 2023
ARFGEF14Oct 2, 2023
ARFGEF1-DT2Mar 5, 2021
ARFGEF24Mar 5, 2021
ARG144Dec 7, 2023
ARHGAP313Feb 19, 2023
ARHGDIA2Feb 21, 2021
ARHGEF104Mar 5, 2021
ARHGEF182Mar 5, 2021
ARHGEF21Feb 21, 2021
ARHGEF62Feb 21, 2021
ARHGEF94Oct 2, 2023
ARID1A32Oct 2, 2023
ARID1B86Dec 14, 2023
ARID216Dec 14, 2023
ARL13B1Mar 5, 2021
ARL61Feb 21, 2021
ARMC52Mar 5, 2021
ARMC92Mar 5, 2021
ARMCX5-GPRASP21Feb 21, 2021
ARNT21Mar 5, 2021
ARPC1B4Mar 12, 2023
ARSA12Mar 5, 2021
ARSB69Dec 7, 2023
ARV12Mar 5, 2021
ARX4Feb 21, 2021
ASAH16Mar 5, 2021
ASCC12Feb 21, 2021
ASCC32Oct 2, 2023
ASH1L18Oct 2, 2023
ASIC4-AS12Feb 21, 2021
ASL86Dec 14, 2023
ASNS3Mar 5, 2021
ASPA54Dec 7, 2023
ASPM21Mar 5, 2021
ASS196Dec 7, 2023
ASTN24Mar 5, 2021
ASXL111Feb 19, 2023
ASXL25Mar 5, 2021
ASXL311Mar 12, 2023
ATAD3A10Feb 19, 2023
ATCAY1Feb 21, 2021
ATF61Mar 5, 2021
ATIC1Feb 21, 2021
ATL14Mar 5, 2021
ATM1239Dec 7, 2023
ATN12Oct 2, 2023
ATP11A1Oct 2, 2023
ATP13A214Feb 19, 2023
ATP1A11Feb 21, 2021
ATP1A1-AS11Feb 21, 2021
ATP1A25Mar 12, 2023
ATP1A312Oct 2, 2023
ATP2A13Mar 5, 2021
ATP2B12Dec 14, 2023
ATP2B21Oct 2, 2023
ATP2B36Feb 19, 2023
ATP5F1A1Mar 5, 2021
ATP5MK1Feb 21, 2021
ATP6V0A23Feb 19, 2023
ATP6V0C1Dec 14, 2023
ATP6V1A1Feb 21, 2021
ATP6V1B11Feb 21, 2021
ATP6V1B21Feb 21, 2021
ATP7A21Dec 7, 2023
ATP7B272Dec 7, 2023
ATP8A24Mar 5, 2021
ATP8B147Dec 7, 2023
ATP8B1-AS118Dec 7, 2023
ATPAF24Mar 5, 2021
ATR1Mar 5, 2021
ATRIP8Mar 5, 2021
ATRIP-TREX18Mar 5, 2021
ATRX18Feb 19, 2023
ATXN7L3-AS11Feb 21, 2021
AUH2Dec 14, 2023
AUTS27Dec 14, 2023
AVIL1Feb 19, 2023
AVPR21Nov 14, 2016
AXDND118Dec 7, 2023
AXIN2191Dec 7, 2023
B3GALNT23Mar 5, 2021
B3GALT21Mar 5, 2021
B3GALT67Oct 2, 2023
B3GAT32Oct 2, 2023
B3GLCT2Oct 2, 2023
B4GALNT15Dec 14, 2023
B4GALT12Mar 5, 2021
B4GALT1-AS11Mar 5, 2021
B4GALT74Feb 19, 2023
B9D13Mar 5, 2021
BACH21Feb 21, 2021
BAG33Mar 5, 2021
BAP1143Dec 7, 2023
BARD1243Dec 7, 2023
BBOF11Mar 5, 2021
BBS155Dec 7, 2023
BBS1085Dec 7, 2023
BBS1265Dec 7, 2023
BBS281Dec 7, 2023
BBS455Dec 7, 2023
BBS52Mar 5, 2021
BBS757Dec 7, 2023
BBS941Dec 7, 2023
BCAP312Feb 21, 2021
BCKDHA70Dec 7, 2023
BCKDHB70Dec 7, 2023
BCKDK3Mar 5, 2021
BCL11A5Jul 1, 2021
BCL11B11Oct 2, 2023
BCOR4Oct 2, 2023
BCORL14Oct 2, 2023
BCS1L59Dec 7, 2023
BDP11Feb 21, 2021
BEST11Feb 21, 2021
BFSP21Mar 5, 2021
BGN4Mar 5, 2021
BICD24Feb 19, 2023
BICRA4Oct 2, 2023
BIN13Mar 5, 2021
BIVM-ERCC516Dec 6, 2021
BLK2Feb 19, 2023
BLM122Dec 7, 2023
BLNK2Mar 5, 2021
BLOC1S31Mar 5, 2021
BLOC1S61Mar 5, 2021
BLTP110Mar 5, 2021
BLVRA1Feb 21, 2021
BMP13Mar 5, 2021
BMP21Mar 5, 2021
BMPR1A101Dec 7, 2023
BMPR1B1Mar 5, 2021
BMPR25Feb 19, 2023
BNC11Feb 21, 2021
BOLA34Feb 21, 2021
BPNT22Feb 19, 2023
BPTF22Oct 2, 2023
BRAF11Mar 5, 2021
BRAT111Feb 19, 2023
BRCA1581Dec 7, 2023
BRCA2955Dec 14, 2023
BRCC31Apr 1, 2019
BRF14Feb 21, 2021
BRIP1361Dec 7, 2023
BRME11Feb 21, 2021
BRPF110Dec 14, 2023
BRWD11Oct 16, 2017
BRWD38Oct 2, 2023
BSCL27Oct 2, 2023
BSN2Dec 14, 2023
BSND1Feb 21, 2021
BTD106Dec 14, 2023
BTK1Mar 5, 2021
BUB1B8Dec 7, 2023
BUB1B-PAK61Feb 10, 2021
C10orf10518Dec 7, 2023
C10orf551Feb 21, 2021
C11orf65480Dec 7, 2023
C12orf575Feb 19, 2023
C12orf601Mar 5, 2021
C17orf10770Dec 7, 2023
C19orf121Feb 21, 2021
C1QC1Feb 21, 2021
C1QTNF3-AMACR1Feb 21, 2021
C1QTNF51Aug 17, 2015
C1S1Oct 2, 2023
C1orf1054Mar 5, 2021
C1orf1671Mar 5, 2021
C21Mar 5, 2021
C2CD33Oct 2, 2023
C38Feb 19, 2023
C4A2Mar 5, 2021
C4B1Mar 5, 2021
C55Feb 19, 2023
C5orf581Dec 14, 2023
C62Dec 14, 2023
C72Mar 5, 2021
C8B2Mar 5, 2021
C91Mar 5, 2021
CA121Feb 21, 2021
CA23Feb 19, 2023
CACNA1A43Dec 14, 2023
CACNA1B4Oct 2, 2023
CACNA1C7Oct 2, 2023
CACNA1C-AS11Feb 21, 2021
CACNA1D4Feb 19, 2023
CACNA1F1Mar 5, 2021
CACNA1G8Mar 5, 2021
CACNA1H18Mar 5, 2021
CACNA1S5Oct 2, 2023
CACNA2D21Feb 21, 2021
CACNB22Feb 19, 2023
CACNB43Feb 19, 2023
CACNG21Oct 2, 2023
CAD17Feb 19, 2023
CALR1Feb 21, 2021
CAMK2G1Feb 19, 2023
CAMTA112Oct 2, 2023
CANT12Mar 5, 2021
CAPN12Feb 19, 2023
CAPN153Feb 19, 2023
CAPN3190Dec 7, 2023
CARD117Mar 5, 2021
CARD11-AS11Feb 21, 2021
CARD141Sep 27, 2019
CARMIL24Dec 14, 2023
CARS29Oct 2, 2023
CARTPT1Mar 5, 2021
CASD14Oct 2, 2023
CASK7Oct 2, 2023
CASP104Oct 2, 2023
CASP142Feb 21, 2021
CASP85Mar 5, 2021
CASQ22Feb 19, 2023
CASR4Oct 2, 2023
CAST1Mar 5, 2021
CBL12Dec 7, 2023
CBLIF1Mar 5, 2021
CBS98Dec 7, 2023
CC2D1A15Mar 5, 2021
CC2D2A16Feb 19, 2023
CCBE13Feb 21, 2021
CCDC1032Mar 5, 2021
CCDC1151Mar 5, 2021
CCDC1411Feb 21, 2021
CCDC1744Oct 2, 2023
CCDC225Oct 2, 2023
CCDC301Feb 21, 2021
CCDC393Oct 2, 2023
CCDC403Mar 5, 2021
CCDC501Mar 5, 2021
CCDC653Mar 5, 2021
CCDC781Mar 5, 2021
CCDC83Mar 5, 2021
CCDC88A1Mar 5, 2021
CCDC88C9Feb 19, 2023
CCDST21Dec 14, 2023
CCM22Mar 5, 2021
CCN63Feb 19, 2023
CCND22Mar 5, 2021
CCNF1Oct 2, 2023
CCNH2Mar 5, 2021
CCNO3Oct 2, 2023
CCT52Mar 5, 2021
CD1512Feb 21, 2021
CD1641Oct 2, 2023
CD192Mar 5, 2021
CD2AP2Feb 21, 2021
CD363Feb 19, 2023
CD3D1Mar 5, 2021
CD3E2Mar 5, 2021
CD3G1Feb 21, 2021
CD401Feb 21, 2021
CD461Feb 21, 2021
CD79A3Mar 5, 2021
CD8A1Mar 5, 2021
CD963Feb 21, 2021
CDAN14Mar 5, 2021
CDC14A2Feb 21, 2021
CDC422Feb 19, 2023
CDC42BPB2Feb 19, 2023
CDC452Mar 5, 2021
CDC7326Dec 7, 2023
CDCA7L1Oct 2, 2023
CDH1168Dec 7, 2023
CDH157Mar 5, 2021
CDH21Feb 19, 2023
CDH23201Dec 7, 2023
CDH23-AS15Dec 7, 2023
CDH33Feb 19, 2023
CDK108Oct 2, 2023
CDK1316Oct 2, 2023
CDK5RAP212Mar 5, 2021
CDK81Feb 19, 2023
CDKL516Dec 14, 2023
CDKN1B39Dec 7, 2023
CDKN1C37Dec 7, 2023
CDKN2A70Dec 7, 2023
CDSN1Feb 21, 2021
CDT11Feb 21, 2021
CEACAM162Mar 5, 2021
CEACAM16-AS12Mar 5, 2021
CEBPA44Dec 7, 2023
CEL2Mar 5, 2021
CENPE4Mar 5, 2021
CENPF15Oct 2, 2023
CENPJ7Mar 5, 2021
CEP1042Mar 5, 2021
CEP1207Oct 2, 2023
CEP1354Mar 5, 2021
CEP1526Oct 2, 2023
CEP1643Feb 19, 2023
CEP290312Dec 7, 2023
CEP413Mar 5, 2021
CEP551Feb 21, 2021
CEP5711Feb 11, 2022
CEP635Mar 5, 2021
CEP781Feb 21, 2021
CEP833Oct 2, 2023
CEP85L2Feb 21, 2021
CERKL67Dec 7, 2023
CERS15Feb 19, 2023
CFAP4102Mar 5, 2021
CFAP431Feb 21, 2021
CFAP441Feb 21, 2021
CFAP44-AS11Feb 21, 2021
CFAP522Feb 19, 2023
CFAP533Feb 19, 2023
CFAP651Feb 21, 2021
CFAP741Oct 2, 2023
CFAP911Feb 19, 2023
CFAP9213Dec 7, 2023
CFAP961Oct 2, 2023
CFH9Oct 2, 2023
CFHR11Feb 21, 2021
CFHR52Feb 21, 2021
CFI3Feb 19, 2023
CFL21Feb 21, 2021
CFTR575Dec 14, 2023
CFTR-AS161Dec 7, 2023
CHAMP13Mar 5, 2021
CHAT46Dec 7, 2023
CHD18Oct 2, 2023
CHD210Dec 14, 2023
CHD36Oct 2, 2023
CHD412Oct 2, 2023
CHD52Oct 2, 2023
CHD733Oct 2, 2023
CHD813Dec 14, 2023
CHEK2296Dec 7, 2023
CHKB3Feb 19, 2023
CHKB-CPT1B3Feb 19, 2023
CHMP1A7Feb 19, 2023
CHRNA12Mar 5, 2021
CHRNA22Feb 19, 2023
CHRNA48Feb 19, 2023
CHRNA71Oct 16, 2017
CHRNB11Feb 19, 2023
CHRNB22Mar 5, 2021
CHRND5Feb 19, 2023
CHRNE119Dec 7, 2023
CHRNG7Oct 2, 2023
CHROMR2Mar 14, 2019
CHST142Mar 5, 2021
CHST62Feb 21, 2021
CIBAR11Feb 19, 2023
CIC12Feb 19, 2023
CIITA6Mar 5, 2021
CIROP2Oct 2, 2023
CIT9Feb 19, 2023
CITED22Dec 14, 2023
CKAP2L3Mar 5, 2021
CLCN16Mar 12, 2023
CLCN25Dec 14, 2023
CLCN43Feb 19, 2023
CLCN53Feb 19, 2023
CLCN73Mar 12, 2023
CLCNKA2Oct 2, 2023
CLDN163Feb 19, 2023
CLEC7A1Feb 21, 2021
CLIC21Feb 21, 2021
CLN359Dec 7, 2023
CLN538Dec 7, 2023
CLN64Oct 2, 2023
CLN82Mar 12, 2023
CLP15Mar 5, 2021
CLPB12Feb 19, 2023
CLRN132Dec 7, 2023
CLRN1-AS12Dec 7, 2023
CLTC3Feb 19, 2023
CNGA11Feb 19, 2023
CNGA35Oct 2, 2023
CNGB12Feb 21, 2021
CNGB31Feb 10, 2021
CNKSR23Feb 21, 2021
CNOT11Feb 19, 2023
CNOT36Oct 2, 2023
CNPY36Oct 2, 2023
CNPY3-GNMT6Oct 2, 2023
CNTN11Feb 21, 2021
CNTN23Mar 5, 2021
CNTNAP13Mar 5, 2021
CNTNAP217Mar 5, 2021
COA71Feb 21, 2021
COA82Mar 5, 2021
COASY4Mar 5, 2021
COCH1Feb 21, 2021
COG17Mar 5, 2021
COG22Feb 21, 2021
COG42Feb 19, 2023
COG54Mar 5, 2021
COG67Feb 19, 2023
COG710Mar 5, 2021
COG83Mar 5, 2021
COL10A11Feb 21, 2021
COL11A112Feb 19, 2023
COL11A24Feb 19, 2023
COL12A19Dec 14, 2023
COL13A13Mar 5, 2021
COL17A11Feb 21, 2021
COL18A13Mar 5, 2021
COL1A124Oct 2, 2023
COL1A213Oct 2, 2023
COL27A14Mar 5, 2021
COL2A16Oct 2, 2023
COL3A114Dec 14, 2023
COL4A119Oct 2, 2023
COL4A26Oct 2, 2023
COL4A2-AS12Feb 19, 2023
COL4A34Mar 5, 2021
COL4A412Feb 19, 2023
COL4A511Oct 2, 2023
COL5A110Oct 2, 2023
COL5A23Feb 19, 2023
COL6A19Feb 19, 2023
COL6A210Mar 5, 2021
COL6A313Feb 19, 2023
COL7A16Mar 12, 2023
COL9A12Mar 5, 2021
COL9A31Nov 14, 2016
COLEC111Feb 21, 2021
COLQ48Dec 7, 2023
COMP1Feb 21, 2021
COPA4Oct 2, 2023
COPB13Oct 2, 2023
COQ28Dec 14, 2023
COQ45Mar 5, 2021
COQ51Oct 2, 2023
COQ61Oct 2, 2023
COQ8A9Oct 2, 2023
COQ8B4Oct 2, 2023
COQ92Mar 5, 2021
CORO1A1Mar 5, 2021
COX1011Oct 2, 2023
COX152Mar 5, 2021
COX202Feb 19, 2023
COX4I21Mar 5, 2021
COX6A12Oct 2, 2023
COX6B11Feb 21, 2021
COX7B1Feb 21, 2021
COX8A1Mar 5, 2021
CP22Dec 7, 2023
CPA64Mar 5, 2021
CPAMD83Feb 19, 2023
CPEB1-AS17Mar 5, 2021
CPLANE119Mar 1, 2024
CPOX1Mar 12, 2023
CPS1104Feb 2, 2024
CPT1A46Dec 7, 2023
CPT276Dec 7, 2023
CR212Feb 19, 2023
CRADD4Mar 5, 2021
CRB1141Dec 7, 2023
CRB27Mar 5, 2021
CRBN6Feb 19, 2023
CREB3L11Mar 5, 2021
CREBBP21Oct 2, 2023
CRIPT3Feb 21, 2021
CRPPA4Feb 21, 2021
CRPPA-AS11Feb 21, 2021
CRTAP1Feb 21, 2021
CRYAB1Mar 5, 2021
CRYBA11Mar 5, 2021
CRYBB21Feb 19, 2023
CRYGC1Mar 5, 2021
CRYGD1Mar 14, 2019
CSF1R9Oct 2, 2023
CSF2RB2Mar 5, 2021
CSF3R4Mar 5, 2021
CSNK2A15Mar 5, 2021
CSNK2B2Feb 19, 2023
CSPP110Feb 19, 2023
CSRP31Feb 21, 2021
CTBP12Feb 19, 2023
CTBP1-AS2Feb 19, 2023
CTC18Dec 14, 2023
CTCF8Feb 19, 2023
CTH1Oct 2, 2023
CTLA42Feb 21, 2021
CTNNA156Dec 7, 2023
CTNNA22Oct 2, 2023
CTNNB18Feb 19, 2023
CTNND12Oct 2, 2023
CTNS71Dec 7, 2023
CTNS-AS129Dec 7, 2023
CTPS11Feb 21, 2021
CTR91Dec 7, 2023
CTRC4Dec 7, 2023
CTSA1Feb 21, 2021
CTSC1Feb 21, 2021
CTSD1Mar 5, 2021
CTSK31Dec 7, 2023
CTU21Feb 21, 2021
CTXN2-AS11Oct 2, 2023
CUBN6Mar 5, 2021
CUL34Feb 19, 2023
CUL4B5Oct 2, 2023
CUL77Mar 5, 2021
CUX15Feb 19, 2023
CUX21Feb 19, 2023
CXCR41Feb 19, 2023
CYBA2Mar 5, 2021
CYCS1Mar 5, 2021
CYFIP26Oct 2, 2023
CYLD50Dec 7, 2023
CYLD-AS210Dec 7, 2023
CYP11A11Mar 5, 2021
CYP11B151Dec 7, 2023
CYP17A161Dec 7, 2023
CYP17A1-AS111Dec 7, 2023
CYP1B157Dec 7, 2023
CYP21A23Oct 2, 2023
CYP24A13Mar 5, 2021
CYP26B11Feb 10, 2021
CYP27A179Dec 7, 2023
CYP27B13Oct 2, 2023
CYP2R11Feb 19, 2023
CYP2U13Mar 5, 2021
CYP2U1-AS11Mar 5, 2021
CYP4F224Mar 5, 2021
CYP7B15Mar 5, 2021
CZ1P-ASNS3Mar 5, 2021
D2HGDH9Dec 14, 2023
DAAM23Oct 2, 2023
DAAM2-AS12Oct 2, 2023
DAG13Oct 2, 2023
DAP31Mar 5, 2021
DARS14Mar 5, 2021
DARS23Feb 19, 2023
DBH2Oct 2, 2023
DBNL3Oct 2, 2023
DBT33Dec 7, 2023
DCAF173Feb 19, 2023
DCAF81Feb 19, 2023
DCC4Mar 5, 2021
DCDC22Mar 5, 2021
DCHS116Oct 2, 2023
DCLRE1C42Dec 7, 2023
DCPS7Mar 5, 2021
DCTN16Oct 2, 2023
DCX2Feb 21, 2021
DDB22Dec 6, 2021
DDC2Feb 19, 2023
DDHD23Oct 2, 2023
DDOST2Mar 5, 2021
DDR24Feb 19, 2023
DDX114Mar 5, 2021
DDX3X13Oct 2, 2023
DDX4169Dec 7, 2023
DDX591Mar 5, 2021
DDX61Feb 19, 2023
DEAF19Feb 19, 2023
DEF62Feb 19, 2023
DELE12Feb 21, 2021
DENND5A5Feb 19, 2023
DEPDC515Dec 14, 2023
DES7Feb 19, 2023
DGAT13Feb 21, 2021
DGKE2Mar 5, 2021
DGUOK3Oct 2, 2023
DHCR243Feb 21, 2021
DHCR750Dec 14, 2023
DHDDS12Dec 7, 2023
DHFR46Dec 7, 2023
DHODH1Feb 19, 2023
DHTKD112Mar 12, 2023
DHX303Mar 5, 2021
DHX375Oct 2, 2023
DIAPH14Mar 5, 2021
DICER1198Dec 7, 2023
DIPK1A5Dec 14, 2023
DIS3L232Dec 7, 2023
DKC13Dec 7, 2023
DLAT3Oct 2, 2023
DLD39Dec 14, 2023
DLEC11Mar 5, 2021
DLG32Oct 2, 2023
DLL14Oct 2, 2023
DLL34Oct 2, 2023
DMD49Dec 7, 2023
DMGDH1Feb 19, 2023
DMXL25Feb 19, 2023
DNA23Mar 5, 2021
DNAAF13Feb 21, 2021
DNAAF111Feb 21, 2021
DNAAF22Feb 19, 2023
DNAAF56Dec 14, 2023
DNAH115Dec 14, 2023
DNAH1120Oct 2, 2023
DNAH171Feb 19, 2023
DNAH21Feb 19, 2023
DNAH514Mar 5, 2021
DNAH98Oct 2, 2023
DNAI11Mar 5, 2021
DNAJB21Aug 17, 2015
DNAJB61Feb 21, 2021
DNAJC121Feb 19, 2023
DNAJC213Mar 5, 2021
DNAJC31Feb 21, 2021
DNAJC61Mar 5, 2021
DNAJC9-AS11Feb 19, 2023
DNHD11Feb 19, 2023
DNM14Oct 2, 2023
DNM1L8Oct 2, 2023
DNM26Mar 5, 2021
DNMT12Mar 5, 2021
DNMT3A1Feb 21, 2021
DNMT3B2Mar 5, 2021
DOCK211Mar 5, 2021
DOCK34Feb 19, 2023
DOCK68Feb 19, 2023
DOCK6-AS11Feb 21, 2021
DOCK78Oct 2, 2023
DOCK822Mar 5, 2021
DOCK8-AS12Feb 21, 2021
DOK768Dec 7, 2023
DOLK1Mar 5, 2021
DONSON4Mar 12, 2023
DPAGT12Mar 5, 2021
DPF22Feb 19, 2023
DPH17Oct 2, 2023
DPM12Feb 21, 2021
DPM21Feb 21, 2021
DPP62Mar 5, 2021
DPYD89Dec 7, 2023
DPYD-AS116Dec 7, 2023
DPYS2Feb 21, 2021
DPYSL52Oct 2, 2023
DRC11Mar 5, 2021
DSC23Oct 2, 2023
DSC31Feb 19, 2023
DSE7Feb 21, 2021
DSG23Feb 19, 2023
DSG2-AS12Feb 19, 2023
DSP9Mar 5, 2021
DSPP2Mar 5, 2021
DST14Oct 2, 2023
DSTYK3Feb 19, 2023
DTNA4Dec 14, 2023
DTNBP11Mar 5, 2021
DUOX22Feb 19, 2023
DUSP293Mar 5, 2021
DUSP62Mar 5, 2021
DVL11Feb 21, 2021
DVL22Dec 7, 2023
DVL32Feb 19, 2023
DYM1Mar 5, 2021
DYNC1H117Oct 2, 2023
DYNC1I21Feb 21, 2021
DYNC2H117Dec 14, 2023
DYNC2I21Feb 21, 2021
DYNC2LI11Feb 21, 2021
DYRK1A9Mar 5, 2021
DYRK1B1Feb 21, 2021
DYSF216Feb 23, 2024
DZIP1L1Feb 21, 2021
EARS211Dec 14, 2023
EBF39Feb 19, 2023
ECEL12Feb 21, 2021
ECHS18Feb 19, 2023
ECM11Feb 21, 2021
EDA1Feb 21, 2021
EDAR2Feb 19, 2023
EDARADD1Feb 21, 2021
EDEM32Oct 2, 2023
EEF1A24Mar 5, 2021
EEF2KMT1Mar 5, 2021
EFCAB13-DT1Mar 5, 2021
EFEMP21Feb 21, 2021
EFHC14Feb 19, 2023
EFL13Mar 5, 2021
EFTUD28Dec 14, 2023
EGFR8Dec 7, 2023
EGFR-AS11Dec 7, 2023
EGR21Oct 2, 2023
EHMT112Oct 2, 2023
EIF2AK12Feb 19, 2023
EIF2AK24Oct 2, 2023
EIF2AK323Dec 7, 2023
EIF2B23Oct 2, 2023
EIF2B32Mar 5, 2021
EIF2B44Oct 2, 2023
EIF2B57Mar 12, 2023
EIF2S31Mar 5, 2021
EIF3F2Mar 12, 2023
EIF3G1Dec 14, 2023
EIF4G11Feb 21, 2021
ELAC25Feb 19, 2023
ELANE3Mar 5, 2021
ELF41Feb 19, 2023
ELMO21Feb 21, 2021
ELN3Feb 19, 2023
ELOVL43Feb 21, 2021
ELP14Feb 11, 2022
ELP210Mar 5, 2021
ELP41Mar 5, 2021
EMC113Oct 2, 2023
EMC1-AS110Oct 2, 2023
EMD2Dec 7, 2023
EME21Feb 21, 2021
EML12Mar 5, 2021
ENAM1Mar 5, 2021
ENG3Dec 7, 2023
ENPP14Mar 5, 2021
ENTPD11Feb 21, 2021
ENTPD1-AS11Feb 21, 2021
ENTPD51Oct 2, 2023
ENTREP21Mar 5, 2021
EP30012Mar 5, 2021
EPB41L12Feb 21, 2021
EPG513Mar 5, 2021
EPHB12Mar 5, 2021
EPHB41Oct 2, 2023
EPHX11Oct 16, 2017
EPHX21Feb 21, 2021
EPM2A1Feb 21, 2021
EPRS18Feb 19, 2023
EPS81Mar 5, 2021
EPS8L22Feb 21, 2021
ERAL11Mar 5, 2021
ERBB41Feb 21, 2021
ERCC11Feb 19, 2023
ERCC2114Dec 7, 2023
ERCC37Dec 7, 2023
ERCC425Dec 7, 2023
ERCC516Dec 6, 2021
ERCC610Mar 5, 2021
ERCC6L23Mar 5, 2021
ERCC81Mar 5, 2021
ERF2Feb 21, 2021
ERLIN21Feb 19, 2023
ERMARD1Feb 21, 2021
ERMP11Feb 21, 2021
ESCO22Feb 21, 2021
ESPN2Oct 2, 2023
ESR11Mar 5, 2021
ESRRB3Feb 21, 2021
ETFA34Dec 7, 2023
ETFB19Dec 7, 2023
ETFDH113Dec 7, 2023
ETHE130Dec 7, 2023
ETV63Mar 5, 2021
EVC5Mar 5, 2021
EVC28Mar 5, 2021
EVI2A1Dec 7, 2023
EXOSC22Feb 19, 2023
EXOSC32Mar 5, 2021
EXOSC52Feb 19, 2023
EXOSC82Feb 21, 2021
EXPH51Feb 21, 2021
EXT169Dec 7, 2023
EXT273Dec 7, 2023
EXTL31Mar 5, 2021
EYA11Feb 19, 2023
EYS316Dec 14, 2023
EZH21Feb 10, 2021
F111Mar 5, 2021
F122Dec 14, 2023
F13B1Mar 5, 2021
F23Oct 2, 2023
F54Oct 2, 2023
F73Oct 2, 2023
F84Feb 19, 2023
FA2H3Mar 5, 2021
FAH74Dec 7, 2023
FAM111A2Mar 5, 2021
FAM111B2Mar 5, 2021
FAM161A53Dec 7, 2023
FAM20A2Dec 7, 2023
FAN11Mar 5, 2021
FANCA265Dec 7, 2023
FANCB4Dec 7, 2023
FANCC83Dec 7, 2023
FANCD295Dec 7, 2023
FANCD2OS28Dec 7, 2023
FANCE49Dec 7, 2023
FANCF28Dec 7, 2023
FANCG76Dec 7, 2023
FANCI115Dec 7, 2023
FANCL43Dec 7, 2023
FANCM33Dec 7, 2023
FAR11Oct 2, 2023
FARS212Oct 2, 2023
FAS1Feb 21, 2021
FASTKD23Feb 19, 2023
FAT21Feb 19, 2023
FAT417Feb 19, 2023
FBLN11Feb 21, 2021
FBLN53Mar 5, 2021
FBN120Dec 14, 2023
FBN26Mar 5, 2021
FBP11Feb 19, 2023
FBXL321Dec 7, 2023
FBXL414Oct 2, 2023
FBXO118Feb 19, 2023
FBXO314Mar 5, 2021
FBXO381Feb 21, 2021
FBXW72Dec 7, 2023
FCGR3A2Mar 5, 2021
FCN31Feb 21, 2021
FCSK5Feb 19, 2023
FDFT12Feb 21, 2021
FDXR4Feb 19, 2023
FECH2Oct 2, 2023
FERMT32Feb 21, 2021
FGD13Feb 19, 2023
FGF122Oct 2, 2023
FGF131Feb 19, 2023
FGF81Mar 5, 2021
FGFR19Oct 2, 2023
FGFR23Nov 23, 2018
FGFR313Feb 19, 2023
FGG1Oct 2, 2023
FH90Dec 7, 2023
FHL13Feb 19, 2023
FHOD31Oct 2, 2023
FIBP2Dec 14, 2023
FIG49Dec 14, 2023
FITM22Feb 19, 2023
FKBP104Feb 21, 2021
FKBP142Feb 21, 2021
FKBP14-AS12Feb 21, 2021
FKRP65Dec 7, 2023
FKTN57Dec 7, 2023
FLCN86Dec 14, 2023
FLG21Dec 14, 2023
FLNA15Oct 2, 2023
FLNB6Feb 19, 2023
FLNB-AS11Feb 19, 2023
FLNC22Dec 14, 2023
FLNC-AS112Oct 2, 2023
FLRT31Feb 21, 2021
FLT42Feb 19, 2023
FLVCR12Mar 5, 2021
FLVCR21Mar 5, 2021
FMN214Feb 19, 2023
FMO31Feb 19, 2023
FMR12Feb 21, 2021
FN11Mar 5, 2021
FOLR11Feb 21, 2021
FOXC23Mar 5, 2021
FOXE13Mar 5, 2021
FOXF12Mar 5, 2021
FOXG16Oct 2, 2023
FOXN17Dec 14, 2023
FOXP17Mar 12, 2023
FOXP23Mar 5, 2021
FOXP35Dec 7, 2023
FOXRED16Feb 19, 2023
FRAS17Oct 2, 2023
FREM17Mar 5, 2021
FREM21Mar 5, 2021
FRMD54Aug 22, 2022
FRMPD48Feb 19, 2023
FRRS1L9Feb 19, 2023
FTCD2Mar 12, 2023
FTO1Feb 21, 2021
FUS1Dec 14, 2023
FUT82Feb 19, 2023
FXN1Mar 5, 2021
FXR11Oct 2, 2023
FYB11Mar 5, 2021
FYCO11Feb 21, 2021
FZD41Mar 5, 2021
FZD61Feb 21, 2021
FZR11Oct 2, 2023
G6PC120Feb 19, 2023
G6PC33Dec 14, 2023
G6PD39Dec 7, 2023
GAA241Dec 7, 2023
GABRA21Oct 2, 2023
GABRB11Mar 5, 2021
GABRB22Feb 21, 2021
GABRB36Oct 2, 2023
GABRD2Mar 5, 2021
GABRG24Oct 2, 2023
GAD11Feb 21, 2021
GALC16Oct 2, 2023
GALE1Feb 21, 2021
GALK135Dec 7, 2023
GALNS3Mar 5, 2021
GALNT12107Dec 7, 2023
GALNT21Feb 19, 2023
GALNT32Feb 21, 2021
GALT96Dec 14, 2023
GAMT46Dec 7, 2023
GAN4Feb 21, 2021
GANAB2Oct 2, 2023
GAPVD11Oct 2, 2023
GAREM232Dec 7, 2023
GARS14Mar 12, 2023
GAS81Mar 5, 2021
GATA11Feb 21, 2021
GATA246Dec 7, 2023
GATA32Oct 2, 2023
GATA49Dec 14, 2023
GATA51Feb 21, 2021
GATA62Feb 19, 2023
GATAD153Dec 7, 2023
GATAD2B6Dec 14, 2023
GATM2Oct 2, 2023
GBA138Dec 14, 2023
GBA26Mar 5, 2021
GBE186Dec 14, 2023
GBF11Oct 2, 2023
GCDH121Dec 7, 2023
GCH12Feb 19, 2023
GCK18Feb 19, 2023
GDAP13Mar 5, 2021
GDF15Feb 19, 2023
GDF21Mar 5, 2021
GDF51Feb 21, 2021
GDF5-AS11Feb 21, 2021
GDF64Mar 12, 2023
GEMIN44Mar 5, 2021
GEMIN53Oct 2, 2023
GEN11Dec 7, 2023
GFAP4Mar 5, 2021
GFER2Oct 16, 2017
GFI12Feb 21, 2021
GFI1B1Feb 19, 2023
GFM187Dec 7, 2023
GFM23Feb 19, 2023
GFPT12Mar 5, 2021
GGA31Feb 21, 2021
GGCX1Mar 5, 2021
GGT11Feb 21, 2021
GH-LCR11Dec 14, 2023
GH14Mar 5, 2021
GHRHR3Mar 5, 2021
GHSR1Mar 5, 2021
GIGYF22Feb 21, 2021
GINS11Mar 5, 2021
GIPC31Feb 21, 2021
GJA13Mar 5, 2021
GJA81Feb 21, 2021
GJB13Feb 21, 2021
GJB230Dec 14, 2023
GJB31Mar 5, 2021
GJC22Mar 5, 2021
GJD2-DT8Feb 19, 2023
GK2Feb 19, 2023
GK-AS11Feb 19, 2023
GLA2Feb 21, 2021
GLB19Mar 5, 2021
GLDC12Oct 2, 2023
GLDN1Feb 21, 2021
GLE11Mar 5, 2021
GLI11Mar 5, 2021
GLI28Oct 2, 2023
GLI31Nov 14, 2016
GLIS22Mar 5, 2021
GLIS38Feb 19, 2023
GLIS3-AS11Feb 21, 2021
GLMN1Feb 19, 2023
GLRX52Feb 21, 2021
GLUD12Feb 21, 2021
GLYCTK4Mar 5, 2021
GM2A2Feb 21, 2021
GML16Dec 7, 2023
GMNN3Jun 23, 2015
GMPPB4Feb 21, 2021
GNAI12Oct 2, 2023
GNAO14Feb 19, 2023
GNAS7Dec 14, 2023
GNB15Feb 19, 2023
GNB41Mar 5, 2021
GNB52Mar 5, 2021
GNE53Dec 7, 2023
GNPAT22Dec 7, 2023
GNPTAB10Mar 5, 2021
GNRHR1Mar 5, 2021
GNS2Feb 21, 2021
GORAB1Mar 5, 2021
GOSR21Feb 19, 2023
GOT22Feb 19, 2023
GP1BA1Mar 5, 2021
GP1BB1Mar 5, 2021
GP61Feb 19, 2023
GPAA15Mar 5, 2021
GPC35Dec 6, 2021
GPC41Feb 21, 2021
GPD14Feb 19, 2023
GPHN69Dec 7, 2023
GPI3Mar 5, 2021
GPIHBP11Mar 12, 2023
GPLD12Feb 21, 2021
GPR171Feb 21, 2021
GPRASP21Feb 21, 2021
GPT23Mar 5, 2021
GPX41Feb 21, 2021
GREB1L3Feb 19, 2023
GRHPR41Dec 7, 2023
GRIA21Feb 19, 2023
GRIA36Dec 14, 2023
GRIA43Feb 19, 2023
GRID23Feb 19, 2023
GRIK211Oct 2, 2023
GRIN112Oct 2, 2023
GRIN2A15Dec 14, 2023
GRIN2B17Oct 2, 2023
GRIN2D7Mar 5, 2021
GRIP11Mar 12, 2023
GRM13Mar 5, 2021
GRN2Feb 21, 2021
GRXCR11Feb 21, 2021
GSDME1Feb 21, 2021
GSEC2Mar 5, 2021
GTPBP32Mar 5, 2021
GUCA1A1Feb 21, 2021
GUCA1ANB-GUCA1A1Feb 21, 2021
GUCY1A12Mar 5, 2021
GUCY2C1Mar 5, 2021
GUCY2D1Feb 21, 2021
GUF12Feb 21, 2021
GUSB2Feb 21, 2021
GYG12Feb 19, 2023
GYS15Oct 2, 2023
GYS22Feb 19, 2023
GZF14Mar 5, 2021
H3-3A6Jul 17, 2021
H3-3B7Feb 19, 2023
H6PD1Feb 21, 2021
HACE11Feb 21, 2021
HADH11Dec 7, 2023
HADHA56Dec 7, 2023
HADHB44Dec 14, 2023
HARS21Feb 19, 2023
HAX13Feb 21, 2021
HBA-LCR2Oct 2, 2023
HBA14Sep 21, 2023
HBA24Sep 21, 2023
HBB49Mar 12, 2023
HCFC17Feb 19, 2023
HCN15Oct 2, 2023
HCN41Feb 19, 2023
HDAC61Mar 5, 2021
HDAC811Feb 19, 2023
HDC1Mar 5, 2021
HECW211Oct 2, 2023
HELLS2Mar 5, 2021
HEPACAM3Mar 5, 2021
HERC117Oct 2, 2023
HERC239Dec 14, 2023
HESX11Feb 21, 2021
HEXA9Feb 19, 2023
HEXB10Oct 2, 2023
HFE3Dec 14, 2023
HFE-AS12Dec 14, 2023
HGF1Feb 19, 2023
HGSNAT2Feb 21, 2021
HIBCH5Feb 19, 2023
HIKESHI1Feb 21, 2021
HIVEP210Mar 5, 2021
HK17Feb 19, 2023
HLCS57Dec 7, 2023
HMBS4Mar 12, 2023
HMGCL30Dec 7, 2023
HMGCS22Feb 19, 2023
HNF1A12Dec 7, 2023
HNF1B2Oct 2, 2023
HNF4A2Dec 14, 2023
HNMT1Mar 5, 2021
HNRNPH21Dec 14, 2023
HNRNPK3Oct 2, 2023
HNRNPK-AS13Oct 2, 2023
HNRNPR1Oct 2, 2023
HNRNPU13Oct 2, 2023
HNRNPUL2-BSCL27Oct 2, 2023
HOMER21Mar 5, 2021
HOXA21Mar 5, 2021
HOXB131Dec 7, 2023
HOXD134Dec 14, 2023
HPDL1Dec 14, 2023
HPS167Dec 7, 2023
HPS388Dec 7, 2023
HPS432Dec 7, 2023
HPS61Feb 21, 2021
HPSE21Feb 21, 2021
HRAS15Oct 2, 2023
HS6ST21Feb 21, 2021
HSALR14Feb 19, 2023
HSD11B21Feb 21, 2021
HSD17B102Feb 21, 2021
HSD17B465Dec 7, 2023
HSD3B21Feb 21, 2021
HSD3B74Oct 2, 2023
HSPB11Feb 21, 2021
HSPB81Feb 21, 2021
HSPD13Feb 21, 2021
HSPG219Oct 2, 2023
HTRA11Feb 21, 2021
HTRA21Feb 21, 2021
HTT8Oct 2, 2023
HUWE17Oct 2, 2023
HYCC12Feb 21, 2021
HYDIN7Feb 19, 2023
IARS112Mar 5, 2021
IARS23Mar 5, 2021
IBA574Feb 19, 2023
ICOS1Feb 21, 2021
IDH23Feb 21, 2021
IDS3Feb 19, 2023
IDUA11Oct 2, 2023
IFIH17Oct 2, 2023
IFNAR21Feb 21, 2021
IFNAR2-IL10RB4Mar 5, 2021
IFT1221Feb 21, 2021
IFT1402Mar 5, 2021
IFT1723Dec 14, 2023
IFT742Feb 19, 2023
IFT811Feb 21, 2021
IGBP12Feb 21, 2021
IGF11Mar 5, 2021
IGF1R11Oct 2, 2023
IGF21Feb 19, 2023
IGFALS3Mar 5, 2021
IGHMBP211Mar 12, 2023
IGLL11Mar 5, 2021
IGSF11Mar 5, 2021
IHH1Feb 21, 2021
IKBKB3Mar 5, 2021
IKBKG1Dec 7, 2023
IKZF11Mar 5, 2021
IKZF51Dec 14, 2023
IL10RA1Feb 21, 2021
IL10RB3Mar 5, 2021
IL12RB13Mar 5, 2021
IL17RA4Mar 5, 2021
IL17RD1Feb 21, 2021
IL1RN1Feb 21, 2021
IL211Mar 5, 2021
IL21-AS11Mar 5, 2021
IL21R3Mar 5, 2021
IL21R-AS12Mar 5, 2021
IL2RA3Mar 5, 2021
IL2RB1Feb 21, 2021
IL2RG1Feb 21, 2021
IL36RN1Feb 21, 2021
IL4I11Feb 21, 2021
IL4R1Feb 19, 2023
IL6ST1Feb 21, 2021
IL7R2Mar 5, 2021
ILDR11Mar 5, 2021
IMPA13Mar 5, 2021
IMPG11Feb 21, 2021
IMPG21Mar 5, 2021
INCA12Feb 21, 2021
INF21Feb 19, 2023
INPP5E5Feb 19, 2023
INPP5K2Mar 5, 2021
INPPL13Mar 5, 2021
INS-IGF21Feb 19, 2023
INSL63Feb 19, 2023
INSR3Mar 5, 2021
INSYN2B1Mar 5, 2021
INTS14Feb 19, 2023
INTS81Feb 19, 2023
INVS3Mar 5, 2021
IQCB135Dec 7, 2023
IQCE1Feb 21, 2021
IQCG1Feb 10, 2021
IQSEC13Feb 19, 2023
IQSEC26Feb 19, 2023
IRAK1BP16Feb 19, 2023
IRAK41Mar 5, 2021
IRF2BP23Mar 5, 2021
IRF2BPL8Feb 21, 2021
IRF61Oct 16, 2017
IRF71Feb 21, 2021
IRS41Feb 21, 2021
IRX54Mar 5, 2021
ISCA22Mar 5, 2021
ISG154Feb 19, 2023
ITCH1Feb 21, 2021
ITGA2B6Feb 19, 2023
ITGA33Feb 21, 2021
ITGA42Dec 7, 2023
ITGA63Feb 21, 2021
ITGA77Mar 5, 2021
ITGA83Mar 5, 2021
ITGB21Mar 5, 2021
ITGB32Feb 19, 2023
ITGB46Oct 2, 2023
ITK2Feb 21, 2021
ITPA3Mar 5, 2021
ITPR119Oct 2, 2023
IVD68Dec 7, 2023
JAG111Oct 2, 2023
JAK11Oct 2, 2023
JAK23Feb 19, 2023
JAK37Mar 5, 2021
JARID21Dec 14, 2023
JMJD81Feb 21, 2021
JPH24Feb 19, 2023
JUP1Feb 21, 2021
KAAG12Mar 5, 2021
KANK15Oct 2, 2023
KANSL111Dec 14, 2023
KARS12Feb 19, 2023
KAT6A16Oct 2, 2023
KAT6B10Mar 5, 2021
KATNB11Mar 5, 2021
KATNIP2Feb 19, 2023
KBTBD132Feb 21, 2021
KCNA11Feb 21, 2021
KCNA22Oct 2, 2023
KCNA42Feb 21, 2021
KCNB19Oct 2, 2023
KCNC12Feb 21, 2021
KCNC33Feb 19, 2023
KCND33Dec 14, 2023
KCNE11Mar 5, 2021
KCNH13Mar 5, 2021
KCNH22Feb 19, 2023
KCNJ104Feb 19, 2023
KCNJ1127Dec 7, 2023
KCNJ131Feb 21, 2021
KCNJ21Mar 14, 2019
KCNJ53Feb 19, 2023
KCNK92Mar 12, 2023
KCNMA11Oct 16, 2017
KCNN21Oct 2, 2023
KCNN31Feb 21, 2021
KCNQ18Dec 14, 2023
KCNQ212Mar 12, 2023
KCNQ35Mar 5, 2021
KCNQ41Mar 5, 2021
KCNQ53Mar 5, 2021
KCNT114Oct 2, 2023
KCNT22Mar 5, 2021
KCNV21Mar 5, 2021
KCTD171Feb 21, 2021
KCTD72Feb 21, 2021
KDM1A2Feb 21, 2021
KDM4B1Dec 14, 2023
KDM5B5Mar 5, 2021
KDM5C10Oct 2, 2023
KDM6A7Oct 2, 2023
KDM6B4Oct 2, 2023
KIAA05867Oct 2, 2023
KIAA07532Mar 5, 2021
KIDINS2206Mar 5, 2021
KIF118Feb 19, 2023
KIF121Feb 19, 2023
KIF149Feb 19, 2023
KIF1A43Dec 14, 2023
KIF1B1Mar 5, 2021
KIF1C5Mar 12, 2023
KIF21B1Feb 19, 2023
KIF225Oct 2, 2023
KIF231Oct 2, 2023
KIF26A2Dec 14, 2023
KIF2A2Feb 19, 2023
KIF4A5Feb 19, 2023
KIF5A4Mar 5, 2021
KIF5C3Feb 19, 2023
KIF717Feb 19, 2023
KIRREL11Oct 2, 2023
KIRREL211Dec 7, 2023
KIRREL31Mar 5, 2021
KISS1R1Feb 21, 2021
KIT86Dec 7, 2023
KLC21Feb 21, 2021
KLF111Feb 21, 2021
KLF71Feb 19, 2023
KLHL101Feb 21, 2021
KLHL153Feb 19, 2023
KLHL31Feb 19, 2023
KLHL406Mar 5, 2021
KLHL411Feb 21, 2021
KLHL71Feb 21, 2021
KLHL91Feb 19, 2023
KMT2A24Oct 2, 2023
KMT2B9Dec 14, 2023
KMT2C15Oct 2, 2023
KMT2D54Dec 14, 2023
KMT2E8Oct 2, 2023
KMT5B2Mar 5, 2021
KNL19Mar 5, 2021
KPNA72Aug 17, 2015
KPTN5Feb 19, 2023
KRAS8Feb 21, 2021
KRIT13Oct 2, 2023
KRT11Feb 19, 2023
KRT101Feb 21, 2021
KRT10-AS11Feb 21, 2021
KRT141Oct 16, 2017
KRT162Mar 5, 2021
KRT182Feb 21, 2021
KRT51Feb 21, 2021
KRT711Feb 21, 2021
KRT81Feb 21, 2021
KRT811Oct 16, 2017
KRT861Oct 16, 2017
KRTAP10-11Mar 5, 2021
KY2Mar 5, 2021
KYNU1Dec 14, 2023
L1CAM5Mar 5, 2021
L2HGDH4Mar 5, 2021
LACC11Feb 21, 2021
LAMA130Oct 2, 2023
LAMA2185Dec 7, 2023
LAMA36Feb 19, 2023
LAMA42Mar 5, 2021
LAMA51Oct 2, 2023
LAMB19Oct 2, 2023
LAMB27Oct 2, 2023
LAMB311Feb 19, 2023
LAMC21Feb 21, 2021
LAMC311Mar 5, 2021
LAMP24Oct 2, 2023
LARGE15Mar 5, 2021
LARP71Feb 21, 2021
LARS15Feb 21, 2021
LARS28Feb 19, 2023
LARS2-AS12Feb 19, 2023
LAS1L3Oct 2, 2023
LAT2Mar 5, 2021
LBR2Feb 21, 2021
LCA541Dec 7, 2023
LCK2Mar 5, 2021
LCP21Dec 14, 2023
LCT1Mar 5, 2021
LDB35Dec 14, 2023
LDHA1Feb 21, 2021
LDLR2Feb 19, 2023
LDLRAD23Mar 5, 2021
LEPR1Feb 21, 2021
LGI11Feb 21, 2021
LGI42Mar 5, 2021
LHX31Feb 21, 2021
LIAS3Feb 21, 2021
LIFR3Feb 21, 2021
LIG41Feb 21, 2021
LIM21Feb 21, 2021
LIMS21Feb 21, 2021
LINC021661Feb 21, 2021
LINC024561Mar 5, 2021
LINGO13Mar 5, 2021
LINS111Mar 5, 2021
LIPA1Feb 19, 2023
LIPE3Feb 21, 2021
LIPE-AS13Feb 21, 2021
LIPT12Oct 16, 2017
LIPT23Mar 5, 2021
LIPT2-AS13Mar 5, 2021
LIX1L-AS11Feb 21, 2021
LMAN2L4Mar 5, 2021
LMBRD15Oct 2, 2023
LMF13Feb 21, 2021
LMNA17Dec 14, 2023
LMNB12Oct 2, 2023
LMNB26Oct 2, 2023
LMOD35Mar 5, 2021
LMX1B3Oct 2, 2023
LNPK1Feb 21, 2021
LOC1002879441Mar 5, 2021
LOC1005060711Feb 21, 2021
LOC1005062352Feb 21, 2021
LOC1005063211Dec 7, 2023
LOC10050734615Dec 7, 2023
LOC1005074432Mar 5, 2021
LOC1014482022Mar 5, 2021
LOC1019270556Oct 2, 2023
LOC1019271571Feb 19, 2023
LOC1019280082Mar 5, 2021
LOC1019283352Dec 14, 2023
LOC1019283501Feb 19, 2023
LOC1019283719Dec 7, 2023
LOC1019285252Feb 21, 2021
LOC1019297101Mar 5, 2021
LOC1019300712Feb 21, 2021
LOC1027235662Dec 7, 2023
LOC10272405816Oct 2, 2023
LOC1053691494Feb 21, 2021
LOC1053715666Feb 19, 2023
LOC1053718561Feb 19, 2023
LOC1053783111Dec 7, 2023
LOC1060501022Feb 19, 2023
LOC1060964162Feb 21, 2021
LOC10609906237Mar 12, 2023
LOC1065017122Oct 2, 2023
LOC1065602112Oct 2, 2023
LOC10662798136Dec 14, 2023
LOC1067217851Dec 7, 2023
LOC1067366141Dec 7, 2023
LOC1067808003Oct 2, 2023
LOC1067808031Oct 2, 2023
LOC10679983342Dec 7, 2023
LOC1068046124Sep 21, 2023
LOC10713351049Mar 12, 2023
LOC10730333866Dec 7, 2023
LOC10730334030Dec 7, 2023
LOC1073033436Dec 7, 2023
LOC1073723151Mar 5, 2021
LOC1074575851Mar 5, 2021
LOC1076524451Mar 5, 2021
LOC1078821261Dec 7, 2023
LOC10798223438Dec 7, 2023
LOC1079880321Oct 2, 2023
LOC1080218461Oct 2, 2023
LOC1082811341Mar 5, 2021
LOC1082811651Feb 21, 2021
LOC1096106311Feb 21, 2021
LOC11000631914Mar 12, 2023
LOC1100112164Dec 7, 2023
LOC1101212881Mar 5, 2021
LOC1101214712Dec 7, 2023
LOC1106739721Dec 7, 2023
LOC1108062637Dec 7, 2023
LOC1114130294Dec 7, 2023
LOC1115892151Dec 7, 2023
LOC11167447265Dec 7, 2023
LOC11167447527Dec 7, 2023
LOC11167447715Dec 7, 2023
LOC1117217051Oct 16, 2017
LOC1118119651Dec 7, 2023
LOC1118119671Feb 21, 2021
LOC1119828694Dec 7, 2023
LOC1121636331Feb 19, 2023
LOC1122725481Feb 21, 2021
LOC1122726211Dec 7, 2023
LOC1124862235Dec 7, 2023
LOC1125298953Feb 19, 2023
LOC1125336721Feb 21, 2021
LOC1125434521Feb 21, 2021
LOC1128409211Mar 12, 2023
LOC1129038391Feb 21, 2021
LOC1129975402Dec 14, 2023
LOC1131749821Feb 21, 2021
LOC11366410611Dec 7, 2023
LOC11368717511Dec 7, 2023
LOC1137882772Mar 5, 2021
LOC1137882973Mar 5, 2021
LOC1138395163Oct 2, 2023
LOC1138457882Oct 2, 2023
LOC1139606111Mar 5, 2021
LOC1148034781Mar 5, 2021
LOC1148278271Oct 2, 2023
LOC1148278514Feb 19, 2023
LOC1153081612Jul 1, 2021
LOC11712559413Dec 7, 2023
LOC1215875742Oct 2, 2023
LOC1217251101Feb 19, 2023
LOC1217407171Mar 5, 2021
LOC1218159746Dec 7, 2023
LOC1218327931Feb 21, 2021
LOC1220568941Feb 21, 2021
LOC12215229617Dec 7, 2023
LOC1227871371Dec 7, 2023
LOC1228612861Mar 5, 2021
LOC1228890111Feb 19, 2023
LOC1238640652Dec 7, 2023
LOC12395621012Dec 14, 2023
LOC1251773938Dec 7, 2023
LOC1251775231Feb 21, 2021
LOC1254462618Dec 7, 2023
LOC1266533981Feb 21, 2021
LOC1268056031Feb 21, 2021
LOC1268056121Mar 5, 2021
LOC1268056552Feb 21, 2021
LOC1268056701Feb 21, 2021
LOC1268057652Feb 19, 2023
LOC1268058221Mar 5, 2021
LOC1268058511Feb 21, 2021
LOC1268058741Mar 5, 2021
LOC1268058841Oct 2, 2023
LOC1268058941Mar 5, 2021
LOC1268059851Feb 21, 2021
LOC1268059944Mar 5, 2021
LOC1268060061Oct 2, 2023
LOC1268060391Feb 19, 2023
LOC1268060632Dec 7, 2023
LOC1268060691Mar 5, 2021
LOC1268061711Mar 5, 2021
LOC1268061721Feb 21, 2021
LOC1268061741Mar 5, 2021
LOC1268062523Feb 19, 2023
LOC1268063062Dec 7, 2023
LOC1268063161Feb 21, 2021
LOC1268063681Dec 7, 2023
LOC1268063731Dec 7, 2023
LOC1268064007Dec 7, 2023
LOC1268064203Feb 19, 2023
LOC1268064211Oct 2, 2023
LOC1268064223Mar 5, 2021
LOC1268064232Feb 21, 2021
LOC1268064258Feb 19, 2023
LOC1268064261Mar 5, 2021
LOC1268064271Feb 19, 2023
LOC1268064281Feb 21, 2021
LOC1268064291Feb 21, 2021
LOC1268064302Feb 21, 2021
LOC1268064321Mar 5, 2021
LOC1268064331Mar 5, 2021
LOC1268065901Feb 19, 2023
LOC1268066582Oct 16, 2017
LOC1268066592Feb 19, 2023
LOC1268066841Mar 5, 2021
LOC1268066891Feb 21, 2021
LOC1268067103Mar 5, 2021
LOC1268067981Feb 21, 2021
LOC1268068072Dec 7, 2023
LOC1268068782Feb 19, 2023
LOC1268069321Mar 5, 2021
LOC1268069512Dec 7, 2023
LOC1268069613Mar 5, 2021
LOC1268071253Feb 21, 2021
LOC1268071372Mar 5, 2021
LOC1268071471Mar 5, 2021
LOC1268073232Mar 5, 2021
LOC1268074377Dec 7, 2023
LOC1268074652Mar 5, 2021
LOC1268075092Mar 5, 2021
LOC1268075561Mar 5, 2021
LOC1268076191Oct 16, 2017
LOC1268595654Feb 19, 2023
LOC1268596462Mar 5, 2021
LOC1268596512Mar 5, 2021
LOC12685969019Dec 7, 2023
LOC1268597842Dec 7, 2023
LOC1268598273Mar 5, 2021
LOC1268598371Feb 21, 2021
LOC1268599612Feb 21, 2021
LOC1268600551Feb 21, 2021
LOC1268601261Feb 21, 2021
LOC1268601301Feb 21, 2021
LOC1268602601Feb 21, 2021
LOC1268604032Mar 5, 2021
LOC12686043810Dec 7, 2023
LOC1268604692Feb 19, 2023
LOC1268607721Feb 21, 2021
LOC1268607921Feb 21, 2021
LOC1268608023Feb 19, 2023
LOC1268609701Feb 21, 2021
LOC1268611101Mar 12, 2023
LOC1268611321Feb 21, 2021
LOC1268612017Dec 7, 2023
LOC1268612051Dec 6, 2021
LOC1268612426Oct 2, 2023
LOC1268612444Dec 7, 2023
LOC1268612581Feb 21, 2021
LOC1268613392Dec 7, 2023
LOC1268613581Feb 21, 2021
LOC1268613652Mar 5, 2021
LOC1268614521Feb 10, 2021
LOC1268615204Dec 14, 2023
LOC1268615251Feb 21, 2021
LOC12686161512Dec 7, 2023
LOC1268618342Dec 6, 2021
LOC1268618962Mar 5, 2021
LOC1268618971Feb 21, 2021
LOC12686189810Oct 2, 2023
LOC1268619361Mar 5, 2021
LOC1268620977Dec 7, 2023
LOC1268621156Dec 7, 2023
LOC1268621231Feb 21, 2021
LOC1268621311Mar 5, 2021
LOC1268622601Feb 21, 2021
LOC1268622649Dec 7, 2023
LOC1268623821Oct 2, 2023
LOC1268623901Feb 19, 2023
LOC1268624221Feb 19, 2023
LOC1268624471Feb 21, 2021
LOC1268624811Feb 21, 2021
LOC1268625002Oct 2, 2023
LOC12686257165Dec 7, 2023
LOC1268625862Nov 23, 2018
LOC1268626061Dec 7, 2023
LOC1268626342Mar 5, 2021
LOC1268626561Feb 19, 2023
LOC1268628531Mar 5, 2021
LOC1268628608Dec 7, 2023
LOC1268628642Feb 21, 2021
LOC1268628651Oct 2, 2023
LOC1268629022Feb 21, 2021
LOC1268629871Feb 21, 2021
LOC1268630081Mar 5, 2021
LOC1268631601Mar 5, 2021
LOC1268631881Feb 19, 2023
LOC1268632121Mar 5, 2021
LOC1268632521Mar 14, 2019
LOC1268632564Mar 12, 2023
LOC1278142972Feb 19, 2023
LOC1278985591Feb 21, 2021
LOC1287722547Dec 7, 2023
LOC1287722551Feb 21, 2021
LOC1293888572Sep 27, 2019
LOC1293892741Feb 21, 2021
LOC1293905144Dec 7, 2023
LOC1293906831Dec 7, 2023
LOC12939090313Dec 7, 2023
LOC1293910645Dec 7, 2023
LOC1299295424Dec 7, 2023
LOC1299300681Mar 5, 2021
LOC1299302451Dec 7, 2023
LOC1299304391Dec 14, 2023
LOC12993044620Dec 7, 2023
LOC1299305617Dec 7, 2023
LOC1299312992Feb 19, 2023
LOC1299315971Feb 19, 2023
LOC1299318941Mar 5, 2021
LOC1299324861Mar 5, 2021
LOC1299327611Mar 5, 2021
LOC1299328122Mar 5, 2021
LOC1299333721Dec 7, 2023
LOC1299335351Feb 21, 2021
LOC1299337074Dec 7, 2023
LOC1299338434Dec 7, 2023
LOC1299340962Feb 19, 2023
LOC1299342361Feb 21, 2021
LOC12993433317Dec 7, 2023
LOC1299351831Feb 21, 2021
LOC1299351841Mar 5, 2021
LOC1299352145Dec 7, 2023
LOC1299352152Dec 7, 2023
LOC1299354111Feb 21, 2021
LOC1299360321Feb 19, 2023
LOC1299362444Dec 7, 2023
LOC1299364341Mar 5, 2021
LOC1299366652Mar 5, 2021
LOC1299367302Mar 5, 2021
LOC1299375861Feb 21, 2021
LOC1299380491Mar 5, 2021
LOC1299921183Dec 7, 2023
LOC1299925856Dec 7, 2023
LOC1299926131Mar 5, 2021
LOC1299928861Feb 21, 2021
LOC1299937342Mar 5, 2021
LOC1299938811Oct 2, 2023
LOC1299938854Dec 7, 2023
LOC1299939181Mar 5, 2021
LOC1299939611Feb 19, 2023
LOC12999412612Dec 7, 2023
LOC1299944603Dec 7, 2023
LOC1299945691Dec 7, 2023
LOC1299956351Feb 19, 2023
LOC1299959782Feb 21, 2021
LOC12999624511Dec 7, 2023
LOC1299966561Feb 19, 2023
LOC1299967272Dec 7, 2023
LOC1299968571Feb 21, 2021
LOC1299974802Feb 19, 2023
LOC1299975232Jul 1, 2021
LOC1299975251Mar 5, 2021
LOC1299977301Dec 14, 2023
LOC1299978271Feb 21, 2021
LOC1299980211Mar 5, 2021
LOC1299982921Oct 2, 2023
LOC1299983421Feb 19, 2023
LOC1299987881Feb 19, 2023
LOC1299987966Dec 7, 2023
LOC1299988332Dec 7, 2023
LOC1299990562Mar 5, 2021
LOC1300005071Mar 5, 2021
LOC1300008321Mar 5, 2021
LOC1300013641Feb 21, 2021
LOC1300014111Feb 10, 2021
LOC1300014381Feb 21, 2021
LOC1300016032Dec 7, 2023
LOC1300016838Dec 14, 2023
LOC1300018621Mar 5, 2021
LOC13000213313Dec 7, 2023
LOC1300022225Dec 7, 2023
LOC1300027191Feb 21, 2021
LOC1300033742Dec 7, 2023
LOC1300045991Feb 21, 2021
LOC13000461410Dec 7, 2023
LOC1300050231Feb 19, 2023
LOC1300050971Mar 5, 2021
LOC1300051938Dec 7, 2023
LOC1300053681Oct 2, 2023
LOC1300054431Dec 7, 2023
LOC1300054442Dec 7, 2023
LOC1300055491Oct 2, 2023
LOC1300060612Mar 5, 2021
LOC1300062069Dec 7, 2023
LOC1300063361Feb 21, 2021
LOC1300064112Mar 5, 2021
LOC1300065081Mar 5, 2021
LOC1300067521Mar 5, 2021
LOC1300067657Dec 7, 2023
LOC1300070262Feb 19, 2023
LOC1300077281Jul 1, 2021
LOC1300086431Mar 5, 2021
LOC1300089872Mar 5, 2021
LOC1300092404Dec 7, 2023
LOC1300093664Dec 7, 2023
LOC1300095731Feb 21, 2021
LOC1300095741Feb 21, 2021
LOC1300095811Feb 21, 2021
LOC1300097471Feb 21, 2021
LOC1300098381Dec 7, 2023
LOC1300098411Feb 21, 2021
LOC1300099138Dec 7, 2023
LOC1300101271Feb 21, 2021
LOC1300553233Dec 7, 2023
LOC1300553871Mar 12, 2023
LOC1300554941Mar 5, 2021
LOC1300557751Mar 5, 2021
LOC1300561751Dec 7, 2023
LOC1300564521Feb 21, 2021
LOC1300564531Feb 21, 2021
LOC1300565191Mar 5, 2021
LOC1300566771Feb 21, 2021
LOC1300568511Mar 5, 2021
LOC1300569213Dec 7, 2023
LOC1300569311Feb 21, 2021
LOC1300574571Feb 21, 2021
LOC1300579541Feb 19, 2023
LOC1300582031Oct 16, 2017
LOC1300582091Dec 7, 2023
LOC1300582102Dec 7, 2023
LOC1300583571Feb 21, 2021
LOC1300583841Feb 21, 2021
LOC1300585433Dec 6, 2021
LOC1300586583Feb 21, 2021
LOC1300586641Feb 21, 2021
LOC1300587121Mar 5, 2021
LOC1300587511Mar 5, 2021
LOC1300589471Feb 19, 2023
LOC1300592241Mar 5, 2021
LOC1300593041Mar 5, 2021
LOC1300593942Mar 5, 2021
LOC1300594401Feb 21, 2021
LOC1300597941Mar 5, 2021
LOC1300598181Feb 21, 2021
LOC13005983711Dec 7, 2023
LOC1300600408Dec 7, 2023
LOC13006004112Dec 7, 2023
LOC1300601136Dec 7, 2023
LOC1300601961Feb 21, 2021
LOC1300603111Mar 5, 2021
LOC1300609033Feb 21, 2021
LOC1300612711Dec 7, 2023
LOC1300614791Mar 5, 2021
LOC1300614961Feb 21, 2021
LOC1300619001Dec 7, 2023
LOC1300619281Feb 19, 2023
LOC1300619731Feb 21, 2021
LOC1300619911Oct 2, 2023
LOC1300620621Feb 21, 2021
LOC1300621452Feb 21, 2021
LOC1300625862Mar 5, 2021
LOC1300628996Dec 7, 2023
LOC13006294512Dec 7, 2023
LOC1300629561Mar 5, 2021
LOC1300635291Mar 5, 2021
LOC1300636482Dec 7, 2023
LOC1300636501Dec 7, 2023
LOC1300637172Mar 5, 2021
LOC1300640744Dec 14, 2023
LOC1300642581Feb 21, 2021
LOC1300642811Mar 5, 2021
LOC1300643572Dec 14, 2023
LOC1300643871Feb 19, 2023
LOC1300644172Oct 2, 2023
LOC1300644721Feb 19, 2023
LOC1300647091Dec 7, 2023
LOC1300647751Feb 21, 2021
LOC1300653231Feb 21, 2021
LOC1300653451Mar 5, 2021
LOC13006543312Dec 7, 2023
LOC1300669401Dec 7, 2023
LOC13006701614Dec 7, 2023
LOC1300673401Feb 21, 2021
LOC13006786210Dec 7, 2023
LOC1300678642Dec 7, 2023
LOC1300682561Feb 21, 2021
LOC1300683961Feb 21, 2021
LOC1300686211Feb 21, 2021
LOC1300687461Feb 21, 2021
LOC1300688861Mar 12, 2023
LOC1320894542Dec 7, 2023
LOC1320897731Oct 2, 2023
LOC1320900592Dec 7, 2023
LOC1320904453Dec 7, 2023
LOC1320904503Dec 7, 2023
LONP17Feb 19, 2023
LOX1Oct 2, 2023
LOXHD18Feb 19, 2023
LPAR61Nov 14, 2016
LPIN15Oct 2, 2023
LPL6Oct 2, 2023
LPP2Feb 21, 2021
LRBA21Dec 14, 2023
LRFN41Feb 21, 2021
LRP212Feb 19, 2023
LRP41Mar 5, 2021
LRP4-AS11Mar 5, 2021
LRP56Oct 2, 2023
LRP61Mar 5, 2021
LRPPRC87Dec 14, 2023
LRRC37A21Feb 19, 2023
LRRC5616Oct 2, 2023
LRRC8A1Feb 21, 2021
LRRK22Feb 21, 2021
LRSAM12Mar 5, 2021
LSS2Mar 5, 2021
LTBP22Feb 11, 2022
LTBP33Mar 5, 2021
LTBP46Oct 2, 2023
LYRM41Feb 21, 2021
LYRM4-AS11Feb 21, 2021
LYRM71Feb 21, 2021
LYST65Dec 7, 2023
LZTR1227Dec 7, 2023
MAB21L21Mar 5, 2021
MACF111Dec 14, 2023
MACROD21Feb 21, 2021
MAF3Mar 5, 2021
MAG2Feb 21, 2021
MAGED21Oct 2, 2023
MAGEL213Dec 14, 2023
MAGT11Oct 2, 2023
MALT16Mar 5, 2021
MALT1-AS12Mar 5, 2021
MAN1B118Oct 2, 2023
MAN2B186Mar 15, 2024
MAN2C11Oct 2, 2023
MANBA4Mar 5, 2021
MAOA1Mar 5, 2021
MAP1B6Feb 19, 2023
MAP2K12Oct 2, 2023
MAP2K27Mar 5, 2021
MAP3K11Mar 5, 2021
MAP3K201Feb 21, 2021
MAP3K20-AS11Feb 21, 2021
MAP3K72Mar 5, 2021
MAPK8IP36Dec 14, 2023
MAPKBP16Oct 2, 2023
MARS14Mar 5, 2021
MARS23Mar 5, 2021
MASP12Feb 21, 2021
MASP22Mar 5, 2021
MAST15Oct 2, 2023
MATN31Feb 21, 2021
MAX14Dec 7, 2023
MBD510Mar 5, 2021
MBL21Feb 21, 2021
MBOAT712Mar 5, 2021
MBTPS210Oct 2, 2023
MC2R2Feb 19, 2023
MC4R3Dec 14, 2023
MCCC182Dec 7, 2023
MCCC287Dec 7, 2023
MCM23Mar 5, 2021
MCM3AP7Feb 19, 2023
MCM3AP-AS13Feb 19, 2023
MCM44Mar 5, 2021
MCM51Mar 5, 2021
MCM71Oct 16, 2017
MCOLN110Oct 7, 2022
MCPH15Mar 5, 2021
MCPH1-AS11Mar 5, 2021
MDH25Mar 5, 2021
MEA15Oct 2, 2023
MECOM2Oct 2, 2023
MECP218Dec 14, 2023
MECR1Feb 21, 2021
MED1210Dec 14, 2023
MED12L2Feb 19, 2023
MED135Oct 2, 2023
MED13L15Oct 2, 2023
MED176Oct 2, 2023
MED2349Dec 7, 2023
MED253Mar 5, 2021
MEF2C3Mar 5, 2021
MEF2C-AS21Feb 21, 2021
MEFV21Dec 7, 2023
MEGF104Oct 2, 2023
MEGF813Oct 2, 2023
MEIS23Feb 19, 2023
MEN180Dec 7, 2023
MERTK3Feb 19, 2023
MESP21Feb 21, 2021
MET136Dec 7, 2023
METTL237Feb 19, 2023
METTL81Feb 21, 2021
MFAP51Mar 5, 2021
MFF3Mar 5, 2021
MFF-DT4Mar 5, 2021
MFN222Oct 2, 2023
MFRP1Aug 17, 2015
MFSD2A1Feb 21, 2021
MFSD82Mar 5, 2021
MGAT22Mar 5, 2021
MGME12Feb 19, 2023
MHRT6Dec 14, 2023
MIB14Oct 2, 2023
MICAL12Feb 21, 2021
MICU13Oct 2, 2023
MID11Feb 21, 2021
MID23Dec 14, 2023
MIF4GD-DT2Mar 5, 2021
MILR13Mar 5, 2021
MINK12Dec 7, 2023
MIPEP14Mar 5, 2021
MIR3936HG1Dec 7, 2023
MIR46851Dec 7, 2023
MIR4733HG1Dec 7, 2023
MIR60841Feb 21, 2021
MIR65051Dec 7, 2023
MIR6511B11Mar 5, 2021
MIR67531Dec 7, 2023
MIR67661Feb 21, 2021
MITD12Oct 16, 2017
MITF2Dec 7, 2023
MKKS40Dec 7, 2023
MKRN21Sep 24, 2014
MKRN31Feb 21, 2021
MKS151Dec 7, 2023
MLC150Dec 7, 2023
MLH1259Dec 7, 2023
MLH32Dec 7, 2023
MLLT101Mar 5, 2021
MLYCD1Feb 19, 2023
MMAA42Dec 7, 2023
MMAB28Dec 7, 2023
MMACHC92Feb 2, 2024
MMADHC25Dec 7, 2023
MME1Feb 19, 2023
MMP131Feb 21, 2021
MMP25Feb 19, 2023
MMP212Feb 21, 2021
MMP92Feb 21, 2021
MMUT5Mar 5, 2021
MN15Oct 2, 2023
MNS11Oct 2, 2023
MOCS125Dec 7, 2023
MOCS24Oct 2, 2023
MOGS3Mar 5, 2021
MORC27Oct 2, 2023
MPC11Feb 21, 2021
MPDU12Mar 5, 2021
MPDU1-AS11Mar 5, 2021
MPDZ18Oct 2, 2023
MPI50Dec 7, 2023
MPIG6B1Feb 21, 2021
MPL6Mar 5, 2021
MPLKIP1Feb 21, 2021
MPV1734Dec 7, 2023
MPZ5Feb 19, 2023
MPZL21Mar 5, 2021
MRAS1Feb 21, 2021
MRE11137Dec 7, 2023
MRPL32Oct 2, 2023
MRPL441Feb 21, 2021
MRPS161Feb 19, 2023
MRPS22Feb 21, 2021
MRPS224Mar 5, 2021
MRPS342Feb 19, 2023
MRPS72Feb 21, 2021
MSH2355Dec 7, 2023
MSH3357Dec 7, 2023
MSH6588Dec 7, 2023
MSL21Apr 8, 2018
MSL31Feb 19, 2023
MSTO14Mar 5, 2021
MT-ATP61Aug 17, 2015
MT-ATP81Aug 17, 2015
MT-CO11Aug 17, 2015
MT-CO21Aug 17, 2015
MT-CO31Aug 17, 2015
MT-ND11Aug 17, 2015
MT-ND21Aug 17, 2015
MT-ND31Aug 17, 2015
MT-ND41Aug 17, 2015
MT-ND4L1Aug 17, 2015
MT-ND51Aug 17, 2015
MT-ND61Aug 17, 2015
MT-TA1Aug 17, 2015
MT-TC1Aug 17, 2015
MT-TD1Aug 17, 2015
MT-TG1Aug 17, 2015
MT-TH1Aug 17, 2015
MT-TI1Aug 17, 2015
MT-TK1Aug 17, 2015
MT-TM1Aug 17, 2015
MT-TN1Aug 17, 2015
MT-TQ1Aug 17, 2015
MT-TR1Aug 17, 2015
MT-TS11Aug 17, 2015
MT-TS21Aug 17, 2015
MT-TW1Aug 17, 2015
MT-TY1Aug 17, 2015
MTFMT7Feb 21, 2021
MTHFD13Mar 12, 2023
MTHFR77Dec 7, 2023
MTM18Dec 7, 2023
MTMR101Mar 5, 2021
MTMR141Feb 21, 2021
MTMR22Feb 21, 2021
MTO110Oct 2, 2023
MTOR9Dec 14, 2023
MTPAP4Mar 5, 2021
MTR1Mar 5, 2021
MTRFR1Oct 16, 2017
MTRR57Feb 23, 2024
MTTP4Feb 21, 2021
MUC11Feb 21, 2021
MUC5B5Mar 5, 2021
MUC5B-AS14Mar 5, 2021
MUSK12Dec 14, 2023
MUTYH222Dec 7, 2023
MVK9Dec 7, 2023
MVP-DT5Oct 2, 2023
MYBPC341Dec 14, 2023
MYCL-AS11Feb 19, 2023
MYF51Feb 21, 2021
MYH117Feb 19, 2023
MYH149Feb 19, 2023
MYH26Oct 2, 2023
MYH32Feb 19, 2023
MYH624Oct 2, 2023
MYH786Dec 14, 2023
MYH97Oct 2, 2023
MYHAS6Oct 2, 2023
MYL31Feb 19, 2023
MYLK3Feb 21, 2021
MYMK3Dec 14, 2023
MYO15A13Feb 19, 2023
MYO18B9Mar 12, 2023
MYO194Feb 19, 2023
MYO1E3Oct 2, 2023
MYO1F1Nov 14, 2016
MYO3A1Mar 5, 2021
MYO5A2Mar 5, 2021
MYO5B2Mar 5, 2021
MYO7A23Mar 12, 2023
MYO9A5Feb 21, 2021
MYOC1Feb 19, 2023
MYOT1Feb 21, 2021
MYPN3Oct 2, 2023
MYRF10Oct 2, 2023
MYSM12Feb 19, 2023
MYT1L4Oct 2, 2023
NAA105Feb 21, 2021
NAA154Oct 2, 2023
NACC11Feb 19, 2023
NADK21Feb 21, 2021
NADSYN12Feb 19, 2023
NAGA1Mar 5, 2021
NAGLU8Oct 2, 2023
NAGS36Dec 7, 2023
NALCN8Oct 2, 2023
NALCN-AS11Mar 5, 2021
NARS11Feb 19, 2023
NARS27Mar 5, 2021
NAXD3Feb 21, 2021
NAXD-AS11Feb 21, 2021
NAXE2Feb 21, 2021
NBAS12Mar 12, 2023
NBEA4Dec 14, 2023
NBEAL24Feb 21, 2021
NBN259Dec 7, 2023
NCAPD23Feb 21, 2021
NCAPD36Mar 5, 2021
NCAPG22Feb 19, 2023
NCAPH2Feb 21, 2021
NCAPH216Dec 7, 2023
NCF22Mar 5, 2021
NCKAP1L1Feb 19, 2023
NDE18Feb 19, 2023
NDRG12Mar 5, 2021
NDST15Mar 5, 2021
NDUFA104Dec 14, 2023
NDUFA115Oct 2, 2023
NDUFA122Mar 5, 2021
NDUFA134Dec 14, 2023
NDUFA21Mar 5, 2021
NDUFA82Dec 14, 2023
NDUFA96Feb 19, 2023
NDUFAF11Feb 19, 2023
NDUFAF22Mar 5, 2021
NDUFAF35Mar 12, 2023
NDUFAF42Mar 5, 2021
NDUFAF548Dec 7, 2023
NDUFAF67Mar 5, 2021
NDUFAF82Feb 19, 2023
NDUFB111Feb 21, 2021
NDUFB31Feb 21, 2021
NDUFS113Oct 2, 2023
NDUFS24Mar 5, 2021
NDUFS32Feb 19, 2023
NDUFS421Dec 7, 2023
NDUFS612Dec 7, 2023
NDUFS73Feb 19, 2023
NDUFS85Dec 14, 2023
NDUFV120Dec 14, 2023
NDUFV23Feb 19, 2023
NDUFV2-AS11Feb 19, 2023
NEB396Dec 7, 2023
NECAP12Mar 5, 2021
NECTIN11Feb 21, 2021
NECTIN42Mar 5, 2021
NEDD4L4Oct 2, 2023
NEFH2Mar 5, 2021
NEFL1Feb 19, 2023
NEK14Feb 19, 2023
NEK21Mar 12, 2023
NEK84Feb 19, 2023
NEK93Mar 5, 2021
NEXMIF15Oct 2, 2023
NEXN9Mar 12, 2023
NF1380Dec 7, 2023
NF247Dec 7, 2023
NFASC5Feb 19, 2023
NFE2L21Mar 5, 2021
NFIA2Feb 21, 2021
NFIX3Feb 19, 2023
NFKB12Feb 21, 2021
NFKB22Feb 21, 2021
NFKBIA1Mar 5, 2021
NFU12Oct 2, 2023
NGF3Mar 5, 2021
NGF-AS13Mar 5, 2021
NGLY17Dec 14, 2023
NHERF12Feb 19, 2023
NHLH11Mar 5, 2021
NHLRC14Oct 2, 2023
NHLRC21Feb 21, 2021
NHP21Feb 10, 2021
NHS4Feb 21, 2021
NICN14Dec 7, 2023
NIN4Mar 5, 2021
NIPAL42Mar 5, 2021
NIPBL16Oct 2, 2023
NIPSNAP3B1Mar 5, 2021
NKAP1Feb 19, 2023
NKIRAS11Feb 21, 2021
NKX2-13Feb 21, 2021
NKX3-21Feb 21, 2021
NKX6-23Feb 19, 2023
NLGN31Feb 21, 2021
NLGN4X3Feb 21, 2021
NLRC43Mar 5, 2021
NLRP11Mar 5, 2021
NLRP126Oct 2, 2023
NLRP33Feb 21, 2021
NLRP71Feb 21, 2021
NNT4Feb 21, 2021
NOBOX1Feb 21, 2021
NOD24Mar 5, 2021
NODAL3Feb 19, 2023
NOL31Mar 5, 2021
NOP561Feb 21, 2021
NOS31Feb 21, 2021
NOTCH120Dec 14, 2023
NOTCH211Oct 2, 2023
NOTCH37Oct 2, 2023
NPC121Mar 5, 2021
NPC23Mar 5, 2021
NPHP152Dec 7, 2023
NPHP34Feb 21, 2021
NPHP3-ACAD116Feb 21, 2021
NPHP3-AS11Feb 21, 2021
NPHP48Feb 19, 2023
NPHS1149Dec 7, 2023
NPHS253Dec 7, 2023
NPPA1Oct 2, 2023
NPPA-AS11Oct 2, 2023
NPR22Mar 5, 2021
NPRL22Feb 19, 2023
NPRL32Oct 2, 2023
NR1H43Dec 22, 2015
NR2C2AP1Feb 21, 2021
NR2E362Dec 7, 2023
NR2F12Feb 19, 2023
NR2F1-AS12Feb 19, 2023
NR2F21Feb 19, 2023
NR3C12Feb 19, 2023
NR3C22Feb 21, 2021
NR4A22Oct 2, 2023
NR5A11Mar 5, 2021
NRAP1Feb 19, 2023
NRL6Mar 12, 2023
NRXN19Mar 5, 2021
NSD122Oct 2, 2023
NSD22Oct 2, 2023
NSDHL2Feb 19, 2023
NSMCE21Mar 5, 2021
NSMCE31Mar 5, 2021
NSUN28Feb 19, 2023
NSUN61Feb 21, 2021
NT5C21Feb 21, 2021
NT5DC11Feb 21, 2021
NTHL1123Dec 7, 2023
NTNG21Feb 21, 2021
NTRK17Mar 5, 2021
NTRK21Dec 14, 2023
NUBPL2Oct 16, 2017
NUP1332Feb 21, 2021
NUP1551Mar 5, 2021
NUP1601Feb 21, 2021
NUP2143Feb 19, 2023
NUP371Feb 21, 2021
NUP621Feb 21, 2021
NUP851Feb 21, 2021
NUP882Feb 19, 2023
NUP931Feb 19, 2023
NUS14Mar 5, 2021
OAT51Dec 7, 2023
OBSL15Mar 12, 2023
OCA280Dec 7, 2023
OCLN2Feb 21, 2021
OCRL5Mar 5, 2021
ODAD11Feb 21, 2021
ODAD21Oct 2, 2023
ODAD34Mar 5, 2021
ODAD41Mar 5, 2021
OFD18Oct 2, 2023
OGDH1Feb 21, 2021
OGT6Dec 14, 2023
OPA15Mar 5, 2021
OPA311Dec 7, 2023
OPHN16Oct 2, 2023
OPLAH2Mar 5, 2021
ORAI13Mar 5, 2021
ORC14Feb 19, 2023
ORC61Mar 5, 2021
OSGEP3Mar 5, 2021
OTC16Dec 14, 2023
OTOA4Feb 19, 2023
OTOF7Mar 12, 2023
OTOG16Feb 19, 2023
OTOGL7Mar 5, 2021
OTUD6B9Mar 5, 2021
OTULIN2Feb 21, 2021
OTX22Feb 19, 2023
OXCT11Feb 21, 2021
OXR11Feb 19, 2023
P2RX21Feb 21, 2021
P2RY121Feb 19, 2023
P3H11Feb 21, 2021
P4HB1Mar 5, 2021
P4HTM3Feb 21, 2021
PACS12Feb 19, 2023
PACS23Feb 19, 2023
PAFAH1B13Oct 16, 2017
PAH256Dec 7, 2023
PAK11Feb 19, 2023
PAK31Mar 5, 2021
PALB2382Dec 7, 2023
PANK25Dec 14, 2023
PAPSS22Feb 21, 2021
PARN2Mar 5, 2021
PARS22Oct 2, 2023
PAX13Feb 21, 2021
PAX33Mar 5, 2021
PAX62Feb 19, 2023
PAX6DRR1Mar 5, 2021
PAX72Feb 21, 2021
PAX82Feb 21, 2021
PAX8-AS11Feb 21, 2021
PBRM11Jul 1, 2021
PBX12Oct 2, 2023
PC37Dec 14, 2023
PCCA81Dec 7, 2023
PCCB78Dec 7, 2023
PCDH125Feb 21, 2021
PCDH15110Dec 7, 2023
PCDH196Oct 2, 2023
PCK11Feb 21, 2021
PCK25Mar 12, 2023
PCLO19Mar 5, 2021
PCNA1Mar 5, 2021
PCNT12Feb 19, 2023
PCOTH1Feb 21, 2021
PCSK11Mar 5, 2021
PCSK93Oct 2, 2023
PCYT1A3Mar 5, 2021
PDCD103Feb 19, 2023
PDE11A3Mar 5, 2021
PDF1Mar 5, 2021
PDGFB1Feb 21, 2021
PDGFRA98Dec 7, 2023
PDGFRB2Oct 2, 2023
PDHA112Mar 12, 2023
PDHB10Dec 7, 2023
PDHX6Dec 14, 2023
PDK1-AS11Feb 21, 2021
PDP11Feb 19, 2023
PDS5A2Apr 8, 2018
PDSS12Mar 5, 2021
PDSS25Oct 2, 2023
PDX11Feb 21, 2021
PDYN1Mar 5, 2021
PDYN-AS11Mar 5, 2021
PDZD77Oct 2, 2023
PDZD93Mar 5, 2021
PEPD1Feb 21, 2021
PERCC11Oct 2, 2023
PEX1171Dec 7, 2023
PEX1045Dec 7, 2023
PEX1234Dec 7, 2023
PEX165Mar 12, 2023
PEX193Mar 5, 2021
PEX232Dec 7, 2023
PEX2620Dec 7, 2023
PEX32Feb 21, 2021
PEX513Oct 2, 2023
PEX6104Dec 7, 2023
PEX754Dec 7, 2023
PFKM42Dec 14, 2023
PGAM23Oct 2, 2023
PGAP17Mar 5, 2021
PGAP21Feb 21, 2021
PGAP34Mar 5, 2021
PGK11Oct 2, 2023
PGM34Mar 5, 2021
PHC12Mar 5, 2021
PHEX3Feb 21, 2021
PHF363Dec 14, 2023
PHF63Feb 19, 2023
PHF88Feb 19, 2023
PHGDH7Mar 12, 2023
PHIP8Feb 19, 2023
PHKA16Oct 2, 2023
PHKA26Dec 14, 2023
PHKA2-AS11Feb 21, 2021
PHKB2Feb 19, 2023
PHKG26Dec 14, 2023
PHOX2B37Dec 7, 2023
PHOX2B-AS15Dec 7, 2023
PHYH25Dec 7, 2023
PI4KA7Feb 19, 2023
PIBF12Mar 5, 2021
PIEZO112Oct 2, 2023
PIEZO212Feb 19, 2023
PIGA5Mar 5, 2021
PIGB3Oct 2, 2023
PIGBOS11Oct 2, 2023
PIGC4Mar 5, 2021
PIGG25Feb 19, 2023
PIGL2Oct 2, 2023
PIGM1Oct 2, 2023
PIGN14Oct 2, 2023
PIGO6Feb 19, 2023
PIGP1Feb 21, 2021
PIGS3Feb 21, 2021
PIGT3Mar 5, 2021
PIGU1Feb 19, 2023
PIGV5Mar 5, 2021
PIGW4Feb 19, 2023
PIGY3Mar 5, 2021
PIK3C2G1Feb 21, 2021
PIK3CA7Dec 14, 2023
PIK3CD5Oct 2, 2023
PIK3R15Oct 2, 2023
PIK3R22Feb 19, 2023
PIK3R55Feb 19, 2023
PINK14Feb 21, 2021
PINK1-AS2Feb 21, 2021
PITPNM31Mar 5, 2021
PITX11Mar 5, 2021
PITX31Oct 2, 2023
PKD124Feb 19, 2023
PKD1-AS13Mar 5, 2021
PKD1L112Oct 2, 2023
PKD1L1-AS11Feb 21, 2021
PKD24Mar 5, 2021
PKD2L2-DT1Feb 21, 2021
PKHD1442Feb 23, 2024
PKLR3Mar 5, 2021
PKP26Dec 14, 2023
PLA2G618Mar 12, 2023
PLA2G71Feb 21, 2021
PLAA4Mar 5, 2021
PLAU1Feb 21, 2021
PLCB15Mar 5, 2021
PLCB41Feb 21, 2021
PLCE15Mar 5, 2021
PLCG29Oct 2, 2023
PLCH21Dec 7, 2023
PLCZ11Feb 21, 2021
PLD19Oct 2, 2023
PLEC19Feb 19, 2023
PLEKHG213Oct 2, 2023
PLEKHG57Feb 19, 2023
PLG3Mar 5, 2021
PLIN12Mar 5, 2021
PLK43Mar 5, 2021
PLN2Feb 21, 2021
PLOD19Oct 2, 2023
PLOD31Mar 5, 2021
PLP110Oct 2, 2023
PLPBP5Mar 5, 2021
PLS32Feb 19, 2023
PLUT1Feb 21, 2021
PLXNA11Feb 19, 2023
PMM297Dec 7, 2023
PMP221Feb 21, 2021
PMPCA5Mar 5, 2021
PMPCB5Mar 5, 2021
PMS12Dec 7, 2023
PMS2318Dec 14, 2023
PNKP7Mar 5, 2021
PNP3Feb 19, 2023
PNPLA22Mar 5, 2021
PNPLA62Feb 21, 2021
PNPLA84Feb 19, 2023
PNPO2Feb 21, 2021
PNPT125Oct 2, 2023
POC1A5Mar 5, 2021
POGZ12Dec 14, 2023
POLA12Feb 19, 2023
POLD175Dec 7, 2023
POLE83Dec 7, 2023
POLG136Dec 7, 2023
POLG23Mar 5, 2021
POLGARF136Dec 7, 2023
POLR1A1Feb 21, 2021
POLR1C17Oct 2, 2023
POLR1D1Mar 5, 2021
POLR2A3Feb 19, 2023
POLR2F4Feb 19, 2023
POLR3A17Mar 12, 2023
POLR3B9Oct 2, 2023
POLR3H6Oct 2, 2023
POLRMT13Dec 14, 2023
POMGNT182Dec 7, 2023
POMGNT25Mar 5, 2021
POMK3Dec 14, 2023
POMP1Oct 2, 2023
POMT184Dec 14, 2023
POMT245Dec 7, 2023
POP11Feb 21, 2021
POR1Feb 21, 2021
PORCN3Dec 14, 2023
POT11Dec 14, 2023
POU3F32Oct 2, 2023
POU4F32Feb 19, 2023
PPCS1Feb 21, 2021
PPM1D3Mar 5, 2021
PPP1R12A1Feb 19, 2023
PPP2CA3Feb 19, 2023
PPP2R1A5Oct 2, 2023
PPP2R3A1Apr 8, 2018
PPP2R5D6Oct 2, 2023
PPP3CA3Apr 16, 2021
PPT142Dec 7, 2023
PQBP16Mar 5, 2021
PRDM162Oct 2, 2023
PRDM51Feb 19, 2023
PRDM61Mar 5, 2021
PRDM82Mar 5, 2021
PREPL2Feb 21, 2021
PRF174Dec 7, 2023
PRICKLE11Oct 2, 2023
PRICKLE22Oct 16, 2017
PRICKLE2-AS11Oct 16, 2017
PRKAG21Feb 10, 2021
PRKAR1A16Dec 7, 2023
PRKAR1B1Dec 14, 2023
PRKCD1Mar 5, 2021
PRKCG2Feb 19, 2023
PRKCSH1Mar 5, 2021
PRKD15Mar 5, 2021
PRKDC14Mar 5, 2021
PRKN4Mar 5, 2021
PRKRA2Mar 14, 2019
PRMT74Mar 5, 2021
PROC1Dec 14, 2023
PROM11Feb 21, 2021
PROP125Dec 7, 2023
PROS11Mar 5, 2021
PRPF41Feb 21, 2021
PRPS14Feb 19, 2023
PRR123Nov 15, 2017
PRRT25Oct 2, 2023
PRSS129Oct 2, 2023
PRSS231Mar 5, 2021
PRUNE14Mar 5, 2021
PRX16Oct 2, 2023
PSAP7Oct 2, 2023
PSAT12Mar 5, 2021
PSMB41Mar 5, 2021
PSMB81Mar 5, 2021
PSMD122Mar 5, 2021
PSORS1C11Feb 21, 2021
PSPH1Mar 5, 2021
PSTPIP11Oct 2, 2023
PTCD33Feb 19, 2023
PTCH1102Dec 7, 2023
PTCH213Dec 7, 2023
PTCHD12Oct 2, 2023
PTCHD1-AS2Feb 21, 2021
PTDSS13Oct 2, 2023
PTEN60Dec 7, 2023
PTGIS1Mar 5, 2021
PTH1R2Feb 19, 2023
PTPN1175Dec 14, 2023
PTPN232Feb 19, 2023
PTPRC6Mar 5, 2021
PTPRO3Oct 2, 2023
PTPRQ1Oct 2, 2023
PTRH21Feb 21, 2021
PTS47Dec 7, 2023
PUF606Oct 2, 2023
PUM13Oct 2, 2023
PURA4Oct 2, 2023
PUS119Dec 7, 2023
PUS73Feb 19, 2023
PYCR14Oct 2, 2023
PYCR22Mar 5, 2021
PYGL8Feb 19, 2023
PYGM107Dec 14, 2023
PYROXD13Mar 5, 2021
PYURF3Mar 5, 2021
PYY3Dec 7, 2023
QARS14Oct 2, 2023
QDPR2Feb 21, 2021
QRICH12Feb 19, 2023
RAB11B1Feb 21, 2021
RAB231Feb 21, 2021
RAB27A1Mar 14, 2019
RAB33A5Dec 7, 2023
RAB3GAP13Feb 21, 2021
RAB3GAP23Mar 5, 2021
RAB9B10Oct 2, 2023
RAC13Oct 2, 2023
RAC31Feb 21, 2021
RAD214Oct 2, 2023
RAD50160Dec 7, 2023
RAD51C168Dec 7, 2023
RAD51D130Dec 7, 2023
RAD51L3-RFFL130Dec 7, 2023
RAF19Feb 19, 2023
RAG180Dec 7, 2023
RAG235Dec 7, 2023
RAI17Oct 2, 2023
RALA1Oct 2, 2023
RALGAPA11Oct 2, 2023
RANBP25Feb 19, 2023
RAPSN53Dec 7, 2023
RARB2Feb 19, 2023
RARS110Feb 19, 2023
RARS2104Dec 7, 2023
RASA13Mar 5, 2021
RB167Dec 7, 2023
RBBP83Mar 5, 2021
RBCK11Mar 5, 2021
RBM104Dec 14, 2023
RBM203Feb 19, 2023
RBM281Feb 21, 2021
RBM8A1Feb 21, 2021
RBMX1Feb 21, 2021
RDH111Feb 21, 2021
RDH1263Dec 7, 2023
RECQL444Dec 7, 2023
REEP15Feb 19, 2023
REEP22Feb 21, 2021
RELN12Feb 19, 2023
RERE15Oct 2, 2023
REST1Feb 10, 2021
RET144Dec 7, 2023
RETREG13Mar 5, 2021
RETREG1-AS12Mar 5, 2021
RFC12Feb 19, 2023
RFT14Oct 2, 2023
RFWD31Feb 19, 2023
RFX63Mar 5, 2021
RFXANK4Feb 19, 2023
RFXAP2Feb 21, 2021
RGR1Mar 5, 2021
RHAG1Feb 19, 2023
RHBDF287Dec 7, 2023
RHOA1Feb 19, 2023
RHOB1Feb 19, 2023
RHOBTB25Oct 2, 2023
RIC12Feb 19, 2023
RIF1135Dec 7, 2023
RIMS12Feb 19, 2023
RINT12Dec 7, 2023
RIPK16Feb 19, 2023
RIPK43Mar 5, 2021
RIPPLY21Feb 19, 2023
RIPPLY2-CYB5R41Feb 19, 2023
RIT13Feb 19, 2023
RLIG117Dec 7, 2023
RLIM2Oct 2, 2023
RMND17Mar 12, 2023
RMND5B1Feb 10, 2021
RNASEH2A2Mar 5, 2021
RNASEH2C4Mar 5, 2021
RNF113A2Feb 21, 2021
RNF1351Mar 5, 2021
RNF143Feb 21, 2021
RNF1684Feb 19, 2023
RNF172Mar 5, 2021
RNF1701Feb 21, 2021
RNF2132Mar 5, 2021
RNF213-AS11Mar 5, 2021
RNF43101Dec 7, 2023
RNPC31Feb 19, 2023
RNU7-12Feb 19, 2023
ROBO11Oct 2, 2023
ROBO21Mar 5, 2021
ROBO31Oct 16, 2017
ROBO41Feb 19, 2023
ROGDI2Mar 5, 2021
ROM11Feb 21, 2021
ROR11Feb 21, 2021
ROR21Feb 21, 2021
RORA5Oct 2, 2023
RORA-AS14Oct 2, 2023
RORB1Oct 2, 2023
RPE6593Dec 7, 2023
RPGR12Dec 7, 2023
RPGRIP13Mar 5, 2021
RPGRIP1L10Mar 5, 2021
RPL102Mar 5, 2021
RPL111Feb 19, 2023
RPL131Feb 21, 2021
RPL151Feb 21, 2021
RPL35A1Feb 10, 2021
RPL36A-HNRNPH23Dec 14, 2023
RPL55Dec 14, 2023
RPS103Feb 10, 2021
RPS10-NUDT33Feb 10, 2021
RPS193Feb 19, 2023
RPS205Dec 7, 2023
RPS231Feb 21, 2021
RPS246Feb 19, 2023
RPS262Feb 19, 2023
RPS6KA31Feb 21, 2021
RPS73Mar 5, 2021
RRAS22Oct 2, 2023
RRM2B8Mar 12, 2023
RS110Dec 14, 2023
RSPH15Mar 5, 2021
RSPH31Mar 5, 2021
RSPRY12Feb 21, 2021
RSRC11Feb 21, 2021
RTEL179Dec 7, 2023
RTEL1-TNFRSF6B79Dec 7, 2023
RTN23Feb 19, 2023
RTN4IP13Oct 2, 2023
RTTN15Feb 19, 2023
RUBCN2Feb 21, 2021
RUNX148Dec 7, 2023
RUNX1-AS14Dec 7, 2023
RUNX22Mar 5, 2021
RUSC216Mar 5, 2021
RXYLT11Mar 5, 2021
RYR157Dec 14, 2023
RYR230Oct 2, 2023
SACS205Dec 7, 2023
SALL11Mar 5, 2021
SALL21Mar 5, 2021
SAMD94Feb 19, 2023
SAMD9L1Dec 14, 2023
SAMHD13Feb 19, 2023
SARM11Feb 21, 2021
SARS23Feb 19, 2023
SATB13Dec 14, 2023
SATB27Dec 14, 2023
SBDS31Dec 7, 2023
SBF16Mar 5, 2021
SBF26Mar 5, 2021
SBF2-AS14Feb 21, 2021
SCAMP47Mar 5, 2021
SCARB22Mar 5, 2021
SCARF23Feb 21, 2021
SCN10A3Feb 19, 2023
SCN11A2Oct 2, 2023
SCN1A27Oct 2, 2023
SCN1A-AS116Oct 2, 2023
SCN1B4Feb 19, 2023
SCN2A16Oct 2, 2023
SCN2B1Mar 5, 2021
SCN3A10Oct 2, 2023
SCN4A12Dec 14, 2023
SCN5A9Oct 2, 2023
SCN8A39Oct 2, 2023
SCN9A20Oct 2, 2023
SCNN1G3Mar 5, 2021
SCO18Feb 19, 2023
SCO224Dec 7, 2023
SCP21Mar 5, 2021
SCYL13Mar 5, 2021
SDCCAG83Feb 21, 2021
SDHA157Dec 7, 2023
SDHAF12Mar 5, 2021
SDHAF232Dec 7, 2023
SDHB84Dec 7, 2023
SDHC36Dec 7, 2023
SDHD26Dec 7, 2023
SEC23A1Mar 5, 2021
SEC23B4Mar 5, 2021
SEC24D1Mar 5, 2021
SEC31A1Feb 21, 2021
SECISBP22Oct 2, 2023
SELENON4Feb 21, 2021
SEMA3A1Apr 1, 2019
SEMA3E4Mar 5, 2021
SEMA4A1Feb 19, 2023
SEPSECS4Feb 19, 2023
SEPT5-GP1BB1Mar 5, 2021
SERAC16Mar 12, 2023
SERPINA131Dec 7, 2023
SERPINA62Feb 21, 2021
SERPINB61Mar 5, 2021
SERPINC11Feb 21, 2021
SERPINE11Mar 5, 2021
SERPINF11Feb 19, 2023
SERPING13Mar 5, 2021
SET2Feb 21, 2021
SETBP117Oct 2, 2023
SETD1A2Feb 19, 2023
SETD1B3Oct 2, 2023
SETD216Oct 2, 2023
SETD518Feb 19, 2023
SETX9Oct 2, 2023
SFTA33Feb 21, 2021
SFTPB1Feb 21, 2021
SFTPC2Oct 2, 2023
SFXN43Mar 5, 2021
SGCA59Dec 7, 2023
SGCB41Dec 7, 2023
SGCD11Dec 7, 2023
SGCE5Oct 2, 2023
SGCG35Dec 7, 2023
SGPL15Oct 2, 2023
SGSH78Dec 7, 2023
SH3PXD2B1Feb 21, 2021
SH3TC28Feb 19, 2023
SHANK21Mar 5, 2021
SHANK39Feb 19, 2023
SHH2Dec 14, 2023
SHOC27Feb 19, 2023
SHOX4Mar 5, 2021
SHQ11Oct 2, 2023
SHROOM410Feb 19, 2023
SI3Feb 19, 2023
SIGMAR11Aug 17, 2015
SIK14Feb 21, 2021
SIL15Mar 5, 2021
SIN3A6Oct 2, 2023
SIPA1L31Mar 5, 2021
SIX13Oct 2, 2023
SKI6Mar 12, 2023
SKIC21Oct 16, 2017
SKIC38Feb 21, 2021
SLC10A23Feb 21, 2021
SLC12A17Oct 2, 2023
SLC12A310Oct 2, 2023
SLC12A510Oct 2, 2023
SLC12A654Dec 7, 2023
SLC13A32Feb 21, 2021
SLC13A510Oct 2, 2023
SLC16A24Feb 19, 2023
SLC17A544Dec 7, 2023
SLC17A91Mar 5, 2021
SLC18A34Mar 5, 2021
SLC19A12Mar 5, 2021
SLC19A21Mar 5, 2021
SLC19A35Feb 19, 2023
SLC1A11Mar 5, 2021
SLC1A22Mar 5, 2021
SLC1A32Feb 19, 2023
SLC1A41Mar 12, 2023
SLC20A21Feb 19, 2023
SLC22A121Feb 21, 2021
SLC22A5112Dec 14, 2023
SLC25A15Mar 5, 2021
SLC25A121Mar 5, 2021
SLC25A1393Dec 7, 2023
SLC25A1532Dec 7, 2023
SLC25A194Oct 2, 2023
SLC25A2029Dec 7, 2023
SLC25A222Feb 19, 2023
SLC25A242Oct 2, 2023
SLC25A381Oct 16, 2017
SLC25A42Dec 14, 2023
SLC25A421Feb 21, 2021
SLC25A461Feb 21, 2021
SLC26A14Feb 21, 2021
SLC26A111Dec 7, 2023
SLC26A275Dec 7, 2023
SLC26A31Feb 21, 2021
SLC26A4202Dec 14, 2023
SLC26A4-AS17Dec 7, 2023
SLC26A51Mar 5, 2021
SLC26A5-AS12Mar 5, 2021
SLC29A32Feb 19, 2023
SLC2A110Oct 2, 2023
SLC2A103Mar 12, 2023
SLC2A21Feb 21, 2021
SLC2A91Nov 14, 2016
SLC30A101Feb 19, 2023
SLC30A21Mar 5, 2021
SLC33A11Feb 21, 2021
SLC34A12Feb 19, 2023
SLC34A21Mar 5, 2021
SLC34A31Feb 19, 2023
SLC35A11Feb 21, 2021
SLC35A24Oct 2, 2023
SLC35A31Oct 7, 2022
SLC35C16Mar 5, 2021
SLC37A468Dec 7, 2023
SLC38A81Mar 5, 2021
SLC39A41Feb 21, 2021
SLC39A84Feb 21, 2021
SLC3A11Oct 2, 2023
SLC44A41Feb 21, 2021
SLC45A19Mar 5, 2021
SLC45A21Nov 14, 2016
SLC46A12Feb 21, 2021
SLC4A13Oct 2, 2023
SLC4A111Feb 21, 2021
SLC4A41Feb 21, 2021
SLC51A1Feb 19, 2023
SLC52A26Feb 19, 2023
SLC5A15Feb 19, 2023
SLC5A21Oct 2, 2023
SLC5A51Mar 5, 2021
SLC5A62Oct 2, 2023
SLC5A72Feb 19, 2023
SLC6A13Mar 5, 2021
SLC6A1-AS11Nov 14, 2016
SLC6A176Mar 5, 2021
SLC6A17-AS12Mar 5, 2021
SLC6A191Mar 5, 2021
SLC6A41Feb 21, 2021
SLC6A58Feb 19, 2023
SLC6A85Dec 7, 2023
SLC6A93Mar 5, 2021
SLC7A755Dec 7, 2023
SLC7A91Dec 14, 2023
SLC9A11Feb 19, 2023
SLC9A31Mar 5, 2021
SLC9A3-AS11Mar 5, 2021
SLC9A62Mar 5, 2021
SLCO1B11Mar 5, 2021
SLCO1B34Feb 19, 2023
SLCO1B3-SLCO1B74Feb 19, 2023
SLCO2A11Mar 5, 2021
SLFN144Oct 2, 2023
SLIT35Oct 2, 2023
SLIT3-AS21Feb 19, 2023
SLITRK11Feb 21, 2021
SLITRK61Mar 5, 2021
SLX443Dec 7, 2023
SMAD32Oct 2, 2023
SMAD443Dec 7, 2023
SMAD68Oct 2, 2023
SMAD91Feb 21, 2021
SMARCA11Feb 19, 2023
SMARCA223Oct 2, 2023
SMARCA4156Dec 7, 2023
SMARCAL12Mar 5, 2021
SMARCB127Dec 7, 2023
SMARCC14Jul 1, 2021
SMARCC210Feb 19, 2023
SMARCE133Dec 7, 2023
SMC1A22Oct 2, 2023
SMC35Feb 21, 2021
SMCHD12Oct 2, 2023
SMG91Feb 21, 2021
SMOC21Feb 21, 2021
SMPD1113Dec 7, 2023
SMPD45Oct 2, 2023
SMS2Oct 2, 2023
SNAP291Feb 21, 2021
SNHG14124Oct 2, 2023
SNIP11Mar 5, 2021
SNTA11Feb 21, 2021
SNX149Dec 6, 2021
SOBP3Mar 5, 2021
SOD12Feb 19, 2023
SON32Oct 2, 2023
SOS116Dec 14, 2023
SOS23Feb 19, 2023
SOX104Feb 19, 2023
SOX114Mar 5, 2021
SOX21Dec 14, 2023
SOX2-OT1Dec 14, 2023
SOX34Oct 2, 2023
SOX41Feb 21, 2021
SOX59Oct 2, 2023
SOX93Oct 2, 2023
SP1105Oct 2, 2023
SP1402Mar 5, 2021
SPAG15Mar 5, 2021
SPAG81Mar 5, 2021
SPARC1Mar 5, 2021
SPART2Feb 19, 2023
SPAST5Dec 14, 2023
SPATA2254Dec 7, 2023
SPATA6L1Mar 5, 2021
SPATA71Mar 5, 2021
SPECC1L1Mar 5, 2021
SPECC1L-ADORA2A1Mar 5, 2021
SPEG10Feb 19, 2023
SPEN6Dec 14, 2023
SPG1120Dec 14, 2023
SPG211Feb 21, 2021
SPG77Mar 12, 2023
SPINK14Dec 7, 2023
SPINK21Feb 21, 2021
SPINK54Mar 5, 2021
SPINT21Feb 21, 2021
SPOP1Feb 19, 2023
SPRED13Mar 5, 2021
SPRY21Feb 21, 2021
SPTA19Mar 5, 2021
SPTAN19Oct 2, 2023
SPTB10Oct 2, 2023
SPTBN17Oct 2, 2023
SPTBN1-AS22Oct 2, 2023
SPTBN29Feb 19, 2023
SPTBN44Feb 19, 2023
SPTLC11Aug 17, 2015
SQSTM13Oct 2, 2023
SRCAP11Feb 19, 2023
SRD5A21Apr 1, 2019
SRD5A33Feb 21, 2021
SREBF12Oct 2, 2023
SRFBP11Oct 2, 2023
SRPK21Feb 21, 2021
SRPX21Feb 19, 2023
SSR42Feb 19, 2023
ST3GAL34Mar 5, 2021
ST3GAL57Feb 21, 2021
STAG114Feb 19, 2023
STAG211Oct 2, 2023
STAMBP5Mar 5, 2021
STAT17Mar 5, 2021
STAT26Dec 14, 2023
STAT34Oct 2, 2023
STAT5B1Feb 21, 2021
STEEP12Feb 21, 2021
STIL5Mar 5, 2021
STIM13Oct 2, 2023
STK1166Dec 7, 2023
STN11Feb 21, 2021
STRA62Mar 5, 2021
STRC3Feb 21, 2021
STRN41Feb 21, 2021
STS1Nov 14, 2016
STT3A2Oct 2, 2023
STUB11Feb 21, 2021
STX1112Dec 7, 2023
STX161Apr 1, 2019
STX1B3Oct 2, 2023
STXBP16Mar 5, 2021
STXBP240Dec 7, 2023
STYXL11Feb 21, 2021
SUCLA24Dec 14, 2023
SUCLG16Feb 19, 2023
SUFU48Dec 7, 2023
SUMF15Mar 12, 2023
SUOX1Feb 21, 2021
SURF14Feb 19, 2023
SVIL2Feb 19, 2023
SYCE28Dec 7, 2023
SYN16Feb 19, 2023
SYNE148Oct 2, 2023
SYNE1-AS12Mar 5, 2021
SYNE211Feb 19, 2023
SYNGAP124Feb 19, 2023
SYNGAP1-AS119Feb 19, 2023
SYNJ13Mar 5, 2021
SYP1Feb 21, 2021
SYT141Mar 5, 2021
SYT21Feb 21, 2021
SZT225Oct 2, 2023
SZT2-AS12Mar 5, 2021
TAB27Feb 19, 2023
TACO12Mar 5, 2021
TAF18Oct 2, 2023
TAF131Feb 21, 2021
TAF22Mar 5, 2021
TAF64Mar 5, 2021
TAFAZZIN2Oct 2, 2023
TALDO17Mar 12, 2023
TANC22Feb 19, 2023
TANGO25Feb 21, 2021
TAP12Oct 2, 2023
TAP22Mar 5, 2021
TAPBP2Mar 5, 2021
TARDBP2Feb 19, 2023
TARS25Mar 5, 2021
TASP11Feb 19, 2023
TAT18Dec 7, 2023
TAT-AS114Dec 7, 2023
TBC1D201Feb 21, 2021
TBC1D234Mar 5, 2021
TBC1D243Feb 21, 2021
TBC1D71Mar 5, 2021
TBC1D7-LOC1001303571Mar 5, 2021
TBCD24Oct 2, 2023
TBCE4Mar 5, 2021
TBCEL-TECTA8Feb 19, 2023
TBCK13Mar 5, 2021
TBK12Feb 21, 2021
TBL1XR14Feb 19, 2023
TBL1XR1-AS12Feb 19, 2023
TBP1Mar 5, 2021
TBX19Oct 2, 2023
TBX151Feb 21, 2021
TBX181Feb 19, 2023
TBX191Oct 16, 2017
TBX23Oct 2, 2023
TBX201Oct 2, 2023
TBX33Feb 19, 2023
TBX3-AS11Feb 21, 2021
TBX56Oct 2, 2023
TBX62Mar 5, 2021
TBXAS12Mar 5, 2021
TBXT1Feb 21, 2021
TCAP1Feb 21, 2021
TCF125Oct 2, 2023
TCF206Oct 2, 2023
TCF46Mar 5, 2021
TCIRG194Dec 7, 2023
TCN23Feb 19, 2023
TCTN13Mar 5, 2021
TCTN23Feb 21, 2021
TCTN33Feb 19, 2023
TDP13Mar 5, 2021
TDP21Feb 21, 2021
TDRD71Feb 21, 2021
TDRD92Feb 21, 2021
TECPR210Mar 5, 2021
TECR2Mar 5, 2021
TECRL2Feb 19, 2023
TECTA8Feb 19, 2023
TEK2Oct 2, 2023
TELO26Feb 19, 2023
TENM32Mar 5, 2021
TENM44Oct 2, 2023
TENT5A1Feb 21, 2021
TERT81Dec 7, 2023
TET25Oct 2, 2023
TET2-AS15Oct 2, 2023
TET32Feb 19, 2023
TEX121Dec 7, 2023
TEX141Feb 19, 2023
TEX151Feb 21, 2021
TEX91Oct 2, 2023
TFAM1Feb 19, 2023
TFAP2A2Mar 5, 2021
TFAP2B3Feb 19, 2023
TFG2Mar 5, 2021
TFR257Dec 7, 2023
TFRC5Mar 5, 2021
TG11Feb 19, 2023
TGFB11Feb 21, 2021
TGFB24Feb 19, 2023
TGFB33Oct 2, 2023
TGFBR16Oct 2, 2023
TGFBR24Feb 21, 2021
TGIF12Dec 14, 2023
TGM196Dec 7, 2023
TGM51Mar 12, 2023
TGM61Mar 5, 2021
TH51Dec 7, 2023
TH2-LCR24Dec 7, 2023
TH2LCRR34Dec 7, 2023
THBD1Feb 21, 2021
THOC24Feb 19, 2023
THOC610Mar 12, 2023
THPO2Feb 19, 2023
THRA1Mar 12, 2023
TIA11Feb 21, 2021
TIMM503Feb 19, 2023
TIMM8A1Oct 2, 2023
TIMMDC17Mar 5, 2021
TINF23Dec 6, 2021
TIRAP-AS11Feb 21, 2021
TJP25Mar 5, 2021
TK23Feb 21, 2021
TKT4Feb 19, 2023
TLK21Mar 14, 2019
TM4SF201Apr 1, 2019
TMC13Oct 2, 2023
TMCO61Mar 5, 2021
TMEM106B2Feb 21, 2021
TMEM126B3Mar 5, 2021
TMEM12745Dec 7, 2023
TMEM132E2Feb 21, 2021
TMEM1651Mar 5, 2021
TMEM2041Mar 5, 2021
TMEM21615Dec 7, 2023
TMEM2317Mar 12, 2023
TMEM2373Mar 12, 2023
TMEM2605Oct 2, 2023
TMEM38B1Feb 21, 2021
TMEM431Oct 2, 2023
TMEM6711Mar 12, 2023
TMEM702Feb 19, 2023
TMEM949Feb 19, 2023
TMIE1Mar 5, 2021
TMLHE1Oct 16, 2017
TMPPE1Mar 5, 2021
TMPRSS153Mar 5, 2021
TMPRSS32Dec 14, 2023
TMPRSS62Feb 21, 2021
TMTC32Mar 5, 2021
TMX21Feb 21, 2021
TMX2-CTNND13Oct 2, 2023
TNC5Feb 19, 2023
TNFAIP32Mar 5, 2021
TNFRSF11A4Mar 5, 2021
TNFRSF11B1Oct 2, 2023
TNFRSF13B11Oct 2, 2023
TNIK3Mar 5, 2021
TNNC13Feb 19, 2023
TNNI22Feb 21, 2021
TNNI35Feb 19, 2023
TNNT12Feb 21, 2021
TNNT22Oct 2, 2023
TNNT34Mar 5, 2021
TNPO33Feb 19, 2023
TNRC6B5Dec 14, 2023
TNXB13Oct 2, 2023
TOE115Dec 7, 2023
TOGARAM11Feb 19, 2023
TOP2B2Feb 19, 2023
TOP3A4Feb 19, 2023
TOR1A3Mar 5, 2021
TOR1AIP11Mar 5, 2021
TP53122Dec 7, 2023
TP53BP11Feb 21, 2021
TP53RK3Mar 5, 2021
TPK13Feb 21, 2021
TPM16Oct 2, 2023
TPM21Feb 21, 2021
TPM32Feb 21, 2021
TPO4Feb 21, 2021
TPP19Mar 5, 2021
TRAF3IP13Oct 2, 2023
TRAF3IP21Mar 5, 2021
TRAF3IP2-AS11Mar 5, 2021
TRAF73Feb 19, 2023
TRAIP1Mar 5, 2021
TRAK13Feb 19, 2023
TRAP11Feb 19, 2023
TRAPPC116Feb 19, 2023
TRAPPC124Mar 5, 2021
TRAPPC141Feb 21, 2021
TRAPPC2L3Feb 19, 2023
TRAPPC921Oct 2, 2023
TRDN2Mar 12, 2023
TREX18Mar 5, 2021
TRIM21Feb 21, 2021
TRIM324Mar 5, 2021
TRIM3741Dec 7, 2023
TRIM541Dec 7, 2023
TRIM81Dec 14, 2023
TRIO23Feb 19, 2023
TRIOBP6Mar 5, 2021
TRIP113Mar 5, 2021
TRIP129Oct 2, 2023
TRIP131Mar 5, 2021
TRIP41Feb 21, 2021
TRIT13Feb 19, 2023
TRMT17Oct 2, 2023
TRMT10A2Feb 21, 2021
TRMT52Mar 5, 2021
TRMU65Dec 7, 2023
TRNT12Feb 21, 2021
TRPA11Mar 5, 2021
TRPC64Mar 5, 2021
TRPM63Mar 5, 2021
TRPM71Feb 21, 2021
TRPS12Feb 21, 2021
TRPV43Feb 19, 2023
TRPV62Feb 21, 2021
TRRAP14Oct 2, 2023
TSC1103Dec 7, 2023
TSC2203Dec 7, 2023
TSEN23Mar 12, 2023
TSEN5412Oct 2, 2023
TSFM35Dec 7, 2023
TSHR3Dec 7, 2023
TSPAN174Dec 7, 2023
TSPAN121Feb 21, 2021
TSPEAR5Mar 5, 2021
TSPEAR-AS11Feb 21, 2021
TSPYL11Feb 21, 2021
TTBK21Feb 21, 2021
TTC195Feb 19, 2023
TTC21B10Oct 2, 2023
TTC21B-AS12Feb 21, 2021
TTC7A6Mar 5, 2021
TTC823Dec 7, 2023
TTI25Mar 5, 2021
TTN266Dec 14, 2023
TTN-AS1155Dec 14, 2023
TTPA31Dec 7, 2023
TTR1Feb 19, 2023
TUBA1A11Dec 14, 2023
TUBA4A1Feb 19, 2023
TUBA84Mar 5, 2021
TUBB6Oct 2, 2023
TUBB12Mar 5, 2021
TUBB2A4Feb 19, 2023
TUBB2B2Feb 21, 2021
TUBB36Oct 2, 2023
TUBB4A7Oct 2, 2023
TUBB4B1Feb 19, 2023
TUBGCP42Feb 21, 2021
TUBGCP611Mar 5, 2021
TUFM3Mar 5, 2021
TULP11Mar 5, 2021
TUSC32Feb 19, 2023
TWIST12Mar 5, 2021
TWIST21Mar 5, 2021
TWNK9Oct 2, 2023
TXN21Feb 21, 2021
TXNL4A1Feb 21, 2021
TYK28Oct 2, 2023
TYMP41Dec 7, 2023
TYR88Dec 7, 2023
UBA11Mar 5, 2021
UBA52Feb 21, 2021
UBAP11Oct 2, 2023
UBE2A1Apr 1, 2019
UBE3A124Oct 2, 2023
UBE3B5Mar 5, 2021
UBN21Mar 14, 2019
UBR14Feb 19, 2023
UBR51Oct 2, 2023
UBTF1Feb 21, 2021
UCN1Dec 7, 2023
UCP31Feb 21, 2021
UFC12Mar 5, 2021
UFM11Feb 21, 2021
UFSP21Oct 2, 2023
UGP21Oct 2, 2023
UGT1A1Oct 7, 2022
UGT1A11Oct 7, 2022
UGT1A101Oct 7, 2022
UGT1A31Oct 7, 2022
UGT1A41Oct 7, 2022
UGT1A51Oct 7, 2022
UGT1A61Oct 7, 2022
UGT1A71Oct 7, 2022
UGT1A81Oct 7, 2022
UGT1A91Oct 7, 2022
UNC13D9Mar 5, 2021
UNC45A1Feb 19, 2023
UNC45B2Feb 19, 2023
UNC8035Oct 2, 2023
UNG3Mar 5, 2021
UPB14Mar 5, 2021
UPF11Feb 19, 2023
UPF3B1Feb 21, 2021
UQCC21Mar 5, 2021
UQCRC11Feb 19, 2023
UQCRC23Mar 5, 2021
UQCRQ2Mar 5, 2021
UROC11Mar 5, 2021
USB13Mar 5, 2021
USH1C62Dec 7, 2023
USH2A570Mar 14, 2024
USH2A-AS143Dec 7, 2023
USH2A-AS231Dec 7, 2023
USP27X2Feb 21, 2021
USP531Feb 19, 2023
USP71Feb 19, 2023
USP9X19Dec 14, 2023
UTP14C1Feb 21, 2021
VAC142Mar 5, 2021
VAPB1Feb 19, 2023
VARS120Oct 2, 2023
VARS215Oct 2, 2023
VCL2Mar 5, 2021
VCP3Feb 19, 2023
VHL64Dec 7, 2023
VIPAS393Feb 21, 2021
VLDLR6Mar 5, 2021
VMA211Mar 5, 2021
VPS118Feb 19, 2023
VPS13A7Mar 5, 2021
VPS13B27Oct 2, 2023
VPS13C3Feb 21, 2021
VPS13D14Dec 14, 2023
VPS33A2Feb 21, 2021
VPS33B3Feb 21, 2021
VPS37A2Feb 19, 2023
VPS453Feb 21, 2021
VPS4A1Oct 2, 2023
VPS535Mar 5, 2021
VRK14Oct 7, 2022
VRK27Dec 7, 2023
VSX21Feb 21, 2021
VWA3B2Mar 5, 2021
VWF11Oct 2, 2023
WAC3Oct 2, 2023
WAPL1Apr 8, 2018
WARS29Feb 19, 2023
WARS2-AS12Feb 19, 2023
WAS2Feb 21, 2021
WASHC45Mar 5, 2021
WASHC54Feb 21, 2021
WASHC5-AS12Feb 21, 2021
WBP21Feb 21, 2021
WDFY38Feb 19, 2023
WDPCP1Oct 16, 2017
WDR194Oct 2, 2023
WDR263Mar 5, 2021
WDR358Oct 2, 2023
WDR372Feb 19, 2023
WDR42Dec 14, 2023
WDR458Mar 12, 2023
WDR6214Oct 2, 2023
WDR735Feb 19, 2023
WDR8118Feb 19, 2023
WFS19Oct 2, 2023
WHRN3Feb 19, 2023
WIPF11Mar 5, 2021
WIPI21Feb 21, 2021
WNK18Mar 5, 2021
WNT10B1Feb 21, 2021
WNT41Feb 19, 2023
WNT5A2Mar 5, 2021
WRAP532Dec 7, 2023
WRN121Dec 7, 2023
WT164Dec 7, 2023
WWOX16Mar 12, 2023
XDH1Feb 21, 2021
XIAP1Feb 21, 2021
XPA24Dec 7, 2023
XPC67Dec 7, 2023
XRCC11Mar 5, 2021
XRCC22Feb 21, 2021
XRCC41Oct 2, 2023
XYLT11Mar 5, 2021
XYLT21Feb 21, 2021
YAP11Mar 5, 2021
YARS12Feb 21, 2021
YARS28Oct 2, 2023
YME1L11Feb 21, 2021
YWHAG2Feb 21, 2021
YY15Feb 19, 2023
YY1AP13Feb 19, 2023
YY24Oct 2, 2023
ZAP703Mar 5, 2021
ZBTB113Feb 21, 2021
ZBTB184Mar 5, 2021
ZBTB205Feb 19, 2023
ZBTB244Feb 19, 2023
ZBTB421Mar 5, 2021
ZBTB471Feb 23, 2023
ZC3H145Dec 14, 2023
ZC4H22Oct 2, 2023
ZCCHC81Feb 21, 2021
ZDHHC151Mar 5, 2021
ZDHHC2428Dec 7, 2023
ZDHHC91Feb 21, 2021
ZEB11Mar 5, 2021
ZEB220Oct 2, 2023
ZFPM23Feb 19, 2023
ZFPM2-AS13Feb 19, 2023
ZFYVE2634Dec 7, 2023
ZIC22Feb 19, 2023
ZIC31Mar 5, 2021
ZMIZ12Dec 14, 2023
ZMPSTE244Feb 19, 2023
ZMYND115Feb 19, 2023
ZNF14211Oct 2, 2023
ZNF1482Mar 5, 2021
ZNF181Feb 21, 2021
ZNF27650Dec 7, 2023
ZNF2921Oct 2, 2023
ZNF3354Feb 21, 2021
ZNF3412Feb 21, 2021
ZNF4233Feb 21, 2021
ZNF4625Feb 19, 2023
ZNF46913Mar 5, 2021
ZNF6272Mar 5, 2021
ZNF6441Mar 5, 2021
ZNF7114Oct 2, 2023
ZNHIT31Mar 5, 2021
ZSWIM63Mar 5, 2021

Condition

NameSubmissionsLast Updated
11p partial monosomy syndrome1Apr 1, 2019
11q partial monosomy syndrome2Apr 1, 2019
15q11q13 microduplication syndrome8Apr 1, 2019
2-aminoadipic 2-oxoadipic aciduria9Mar 12, 2023
2-hydroxyglutaric aciduria5Mar 5, 2021
3 beta-Hydroxysteroid dehydrogenase deficiency1Feb 21, 2021
3-Methylglutaconic aciduria type 22Oct 2, 2023
3-Methylglutaconic aciduria type 310Dec 7, 2023
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency1Apr 1, 2019
3-hydroxy-3-methylglutaryl-CoA synthase deficiency2Feb 19, 2023
3-methylcrotonyl-CoA carboxylase 1 deficiency82Dec 7, 2023
3-methylcrotonyl-CoA carboxylase 2 deficiency87Dec 7, 2023
3-methylglutaconic aciduria type 12Dec 14, 2023
3-methylglutaconic aciduria type 81Feb 21, 2021
3-methylglutaconic aciduria type 93Feb 19, 2023
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome6Mar 12, 2023
3-methylglutaconic aciduria, type VIIB12Feb 19, 2023
3M syndrome 17Mar 5, 2021
3M syndrome 25Mar 12, 2023
3M syndrome 33Mar 5, 2021
3MC syndrome 12Feb 21, 2021
3MC syndrome 21Feb 21, 2021
46,XX sex reversal 41Mar 5, 2021
46,XY sex reversal 61Mar 5, 2021
4p partial monosomy syndrome4Feb 21, 2021
5-Oxoprolinase deficiency2Mar 5, 2021
5p partial monosomy syndrome2Apr 1, 2019
6-Pyruvoyl-tetrahydrobiopterin synthase deficiency47Dec 7, 2023
8q24.3 microdeletion syndrome7Oct 2, 2023
ACTB-related BAFopathy9Jul 1, 2021
ACTH-independent macronodular adrenal hyperplasia 22Mar 5, 2021
ACTL6A-related BAFopathy3Jul 1, 2021
ACTL6B-related BAFopathy4Jul 1, 2021
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder6Mar 5, 2021
AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome14Oct 2, 2023
AICA-ribosiduria1Feb 21, 2021
ALDH18A1-related de Barsy syndrome1Feb 21, 2021
ALG1-congenital disorder of glycosylation4Oct 2, 2023
ALG11-congenital disorder of glycosylation3Mar 5, 2021
ALG12-congenital disorder of glycosylation4Mar 5, 2021
ALG2-congenital disorder of glycosylation3Mar 5, 2021
ALG3-congenital disorder of glycosylation5Feb 19, 2023
ALG6-congenital disorder of glycosylation 1C53Dec 7, 2023
ALG8 congenital disorder of glycosylation7Oct 2, 2023
ALG9 congenital disorder of glycosylation4Feb 19, 2023
ANE syndrome1Feb 21, 2021
ANO5-related muscular dystrophy1Oct 2, 2023
ARID1A-related BAFopathy10Jul 1, 2021
ARID1B-related BAFopathy47Jul 1, 2021
ARID2-related BAFopathy8Jul 1, 2021
ASCC3-related disorder2Oct 2, 2023
Aarskog syndrome3Feb 19, 2023
Abdominal obesity-metabolic syndrome 31Feb 21, 2021
Abetalipoproteinaemia4Feb 21, 2021
Abnormal skeletal morphology2Jan 10, 2017
Abnormality of vision3Nov 15, 2017
Abortive cerebellar ataxia1Feb 10, 2021
Absence seizure3Feb 19, 2023
Acetyl-CoA: carboxylase deficiency1Feb 21, 2021
Achondrogenesis type II1Feb 21, 2021
Achondrogenesis, type IA3Mar 5, 2021
Achondrogenesis, type IB68Dec 7, 2023
Achondroplasia7Feb 19, 2023
Achromatopsia 25Oct 2, 2023
Achromatopsia 31Feb 10, 2021
Achromatopsia 71Mar 5, 2021
Acquired hemoglobin H disease1Feb 21, 2021
Acquired polycythemia vera1Feb 21, 2021
Acral peeling skin syndrome1Mar 12, 2023
Acrocallosal syndrome3Feb 19, 2023
Acrocapitofemoral dysplasia1Feb 21, 2021
Acrocephalosyndactyly type I1Nov 23, 2018
Acrodysostosis 1 with or without hormone resistance14Dec 7, 2023
Acrofacial dysostosis Cincinnati type1Feb 21, 2021
Acromelic frontonasal dysostosis3Mar 5, 2021
Acromesomelic dysplasia 1, Maroteaux type2Mar 5, 2021
Acromesomelic dysplasia 31Mar 5, 2021
Acromicric dysplasia1Feb 21, 2021
Actin accumulation myopathy11Mar 12, 2023
Action myoclonus-renal failure syndrome2Mar 5, 2021
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins3Feb 21, 2021
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome3Mar 5, 2021
Acute intermittent porphyria3Mar 12, 2023
Acute lymphoid leukemia1Feb 21, 2021
Acute myeloid leukemia142Dec 7, 2023
Acute rhabdomyolysis4Sep 3, 2015
Acyl-CoA dehydrogenase 9 deficiency81Dec 7, 2023
Acyl-CoA oxidase deficiency4Feb 19, 2023
Adams-Oliver syndrome 13Feb 19, 2023
Adams-Oliver syndrome 28Feb 19, 2023
Adams-Oliver syndrome 56Dec 14, 2023
Adenosine kinase deficiency1Feb 21, 2021
Adenylosuccinate lyase deficiency9Oct 2, 2023
Adrenocortical carcinoma, hereditary112Dec 7, 2023
Adrenoleukodystrophy28Dec 7, 2023
Adult hypophosphatasia136Dec 7, 2023
Adult polyglucosan body disease1Feb 21, 2021
Adult-onset autosomal dominant demyelinating leukodystrophy2Oct 2, 2023
Agammaglobulinemia 2, autosomal recessive1Mar 5, 2021
Agammaglobulinemia 3, autosomal recessive3Mar 5, 2021
Agammaglobulinemia 4, autosomal recessive2Mar 5, 2021
Agammaglobulinemia 5, autosomal dominant1Feb 21, 2021
Age related macular degeneration 92Feb 19, 2023
Agenesis of corpus callosum, cardiac, ocular, and genital syndrome1Feb 19, 2023
Agenesis of the corpus callosum with peripheral neuropathy53Dec 7, 2023
Aicardi-Goutieres syndrome 18Mar 5, 2021
Aicardi-Goutieres syndrome 34Mar 5, 2021
Aicardi-Goutieres syndrome 42Mar 5, 2021
Aicardi-Goutieres syndrome 53Feb 19, 2023
Aicardi-Goutieres syndrome 66Oct 2, 2023
Aicardi-Goutieres syndrome 74Mar 5, 2021
Aicardi-Goutieres syndrome 92Feb 19, 2023
Al Kaissi syndrome8Oct 2, 2023
Al-Raqad syndrome7Mar 5, 2021
Alagille syndrome due to a JAG1 point mutation10Oct 2, 2023
Alagille syndrome due to a NOTCH2 point mutation6Oct 2, 2023
Alazami-Yuan syndrome4Mar 5, 2021
Aldosterone-producing adenoma with seizures and neurological abnormalities4Feb 19, 2023
Alexander disease4Mar 5, 2021
Alkaline ceramidase 3 deficiency1Feb 21, 2021
Alkuraya-Kucinskas syndrome10Mar 5, 2021
Allan-Herndon-Dudley syndrome4Feb 19, 2023
Alopecia-intellectual disability syndrome 12Mar 5, 2021
Alpha thalassemia-X-linked intellectual disability syndrome10Feb 19, 2023
Alpha-1-antitrypsin deficiency31Dec 7, 2023
Alpha-N-acetylgalactosaminidase deficiency type 21Mar 5, 2021
Alpha-methylacyl-CoA racemase deficiency1Feb 21, 2021
Alstrom syndrome17Feb 19, 2023
Alternating hemiplegia of childhood 11Feb 21, 2021
Alternating hemiplegia of childhood 24Feb 19, 2023
Alveolar capillary dysplasia with pulmonary venous misalignment2Mar 5, 2021
Alveolar rhabdomyosarcoma1Feb 10, 2021
Alzheimer disease2Feb 21, 2021
Amelocerebrohypohidrotic syndrome2Mar 5, 2021
Amelogenesis imperfecta - hypoplastic autosomal dominant - local1Mar 5, 2021
Amelogenesis imperfecta type 1A3Mar 5, 2021
Amelogenesis imperfecta type 1G1Feb 19, 2023
Aminoacylase 1 deficiency6Mar 5, 2021
Aminoglycoside-induced deafness62Dec 7, 2023
Amish lethal microcephaly2Mar 5, 2021
Amyotrophic lateral sclerosis type 11Feb 21, 2021
Amyotrophic lateral sclerosis type 102Feb 19, 2023
Amyotrophic lateral sclerosis type 161Aug 17, 2015
Amyotrophic lateral sclerosis type 191Feb 21, 2021
Amyotrophic lateral sclerosis type 2, juvenile1Feb 19, 2023
Amyotrophic lateral sclerosis type 221Feb 19, 2023
Amyotrophic lateral sclerosis type 43Oct 2, 2023
Amyotrophic lateral sclerosis type 515Dec 14, 2023
Amyotrophic lateral sclerosis type 61Dec 14, 2023
Amyotrophic lateral sclerosis type 81Feb 19, 2023
Amyotrophic lateral sclerosis, susceptibility to, 241Feb 19, 2023
Amyotrophic lateral sclerosis-parkinsonism-dementia complex1Feb 21, 2021
Analbuminemia1Feb 19, 2023
Anauxetic dysplasia 21Feb 21, 2021
Andersen Tawil syndrome1Mar 14, 2019
Androgen resistance syndrome2Oct 2, 2023
Anemia, congenital dyserythropoietic, type 1a4Mar 5, 2021
Anemia, nonspherocytic hemolytic, due to G6PD deficiency6Oct 2, 2023
Aneurysm-osteoarthritis syndrome2Oct 2, 2023
Angelman syndrome130Oct 2, 2023
Aniridia 11Feb 19, 2023
Aniridia 21Mar 5, 2021
Anophthalmia/microphthalmia-esophageal atresia syndrome1Dec 14, 2023
Anterior segment dysgenesis 652Dec 7, 2023
Anterior segment dysgenesis 83Feb 19, 2023
Anxiety1Feb 21, 2021
Aortic aneurysm, familial thoracic 101Oct 2, 2023
Aortic aneurysm, familial thoracic 47Feb 19, 2023
Aortic aneurysm, familial thoracic 61Feb 19, 2023
Aortic aneurysm, familial thoracic 73Feb 21, 2021
Aortic aneurysm, familial thoracic 91Mar 5, 2021
Aortic valve disease 114Oct 2, 2023
Aortic valve disease 28Oct 2, 2023
Aortic valve disease 31Feb 19, 2023
Aplastic anemia346Dec 7, 2023
Apparent mineralocorticoid excess1Feb 21, 2021
Arginase deficiency44Dec 7, 2023
Arginine:glycine amidinotransferase deficiency1Feb 21, 2021
Argininosuccinate lyase deficiency86Dec 14, 2023
Arrhinia with choanal atresia and microphthalmia syndrome1Feb 21, 2021
Arrhythmogenic cardiomyopathy with wooly hair and keratoderma3Mar 5, 2021
Arrhythmogenic right ventricular dysplasia 13Oct 2, 2023
Arrhythmogenic right ventricular dysplasia 102Feb 19, 2023
Arrhythmogenic right ventricular dysplasia 113Oct 2, 2023
Arrhythmogenic right ventricular dysplasia 121Feb 21, 2021
Arrhythmogenic right ventricular dysplasia 213Feb 19, 2023
Arrhythmogenic right ventricular dysplasia 84Mar 5, 2021
Arrhythmogenic right ventricular dysplasia 96Dec 14, 2023
Arterial calcification, generalized, of infancy, 14Mar 5, 2021
Arterial calcification, generalized, of infancy, 25Oct 2, 2023
Arterial tortuosity syndrome3Mar 12, 2023
Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect2Mar 5, 2021
Arthrogryposis multiplex congenita 3, myogenic type6Feb 19, 2023
Arthrogryposis multiplex congenita 6352Dec 7, 2023
Arthrogryposis, Perthes disease, and upward gaze palsy3Mar 5, 2021
Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development1Apr 16, 2021
Arthrogryposis, distal, type 1A1Oct 16, 2017
Arthrogryposis, distal, type 2B22Feb 21, 2021
Arthrogryposis, distal, with impaired proprioception and touch5Feb 19, 2023
Arthrogryposis, renal dysfunction, and cholestasis 13Feb 21, 2021
Arthrogryposis, renal dysfunction, and cholestasis 23Feb 21, 2021
Arts syndrome4Feb 19, 2023
Aspartylglucosaminuria41Dec 7, 2023
Asphyxiating thoracic dystrophy 317Dec 14, 2023
Asphyxiating thoracic dystrophy 42Feb 21, 2021
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome30Oct 2, 2023
Ataxia - oculomotor apraxia type 46Mar 5, 2021
Ataxia with oculomotor apraxia type 35Feb 19, 2023
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia2Mar 5, 2021
Ataxia-pancytopenia syndrome1Dec 14, 2023
Ataxia-telangiectasia syndrome39Mar 12, 2023
Ataxia-telangiectasia-like disorder 1137Dec 7, 2023
Ataxia-telangiectasia-like disorder 21Mar 5, 2021
Ateleiotic dwarfism2Mar 5, 2021
Atelosteogenesis type I5Mar 5, 2021
Atelosteogenesis type II3Feb 19, 2023
Atrial fibrillation, familial, 103Feb 21, 2021
Atrial fibrillation, familial, 111Apr 1, 2019
Atrial fibrillation, familial, 123Oct 2, 2023
Atrial fibrillation, familial, 141Mar 5, 2021
Atrial fibrillation, familial, 151Mar 5, 2021
Atrial fibrillation, familial, 31Feb 21, 2021
Atrial fibrillation, familial, 61Oct 2, 2023
Atrial fibrillation, familial, 91Mar 14, 2019
Atrial septal defect 21Feb 21, 2021
Atrial septal defect 311Oct 2, 2023
Atrial septal defect 41Oct 2, 2023
Atrial septal defect 53Feb 19, 2023
Atrial septal defect 81Mar 5, 2021
Atrioventricular septal defect and common atrioventricular junction1Mar 5, 2021
Atypical behavior3Mar 19, 2021
Atypical glycine encephalopathy3Mar 5, 2021
Atypical hemolytic-uremic syndrome with C3 anomaly3Feb 19, 2023
Atypical hemolytic-uremic syndrome with I factor anomaly2Feb 21, 2021
Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly1Feb 21, 2021
Au-Kline syndrome3Oct 2, 2023
Auditory neuropathy, autosomal dominant 31Oct 2, 2023
Auditory neuropathy-optic atrophy syndrome4Feb 19, 2023
Auriculocondylar syndrome 21Feb 21, 2021
Autism5Nov 15, 2017
Autism spectrum disorder1Mar 14, 2019
Autism spectrum disorder - epilepsy - arthrogryposis syndrome1Oct 7, 2022
Autism spectrum disorder due to AUTS2 deficiency7Dec 14, 2023
Autism, susceptibility to, 171Mar 5, 2021
Autism, susceptibility to, X-linked 11Feb 21, 2021
Autism, susceptibility to, X-linked 23Feb 21, 2021
Autism, susceptibility to, X-linked 42Oct 2, 2023
Autistic behavior3Dec 14, 2020
Autoimmune disease, multisystem, infantile-onset, 22Mar 5, 2021
Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome2Mar 5, 2021
Autoimmune interstitial lung disease-arthritis syndrome4Oct 2, 2023
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency2Feb 21, 2021
Autoimmune lymphoproliferative syndrome type 11Feb 21, 2021
Autoimmune lymphoproliferative syndrome type 2A4Oct 2, 2023
Autoimmune lymphoproliferative syndrome type 2B5Mar 5, 2021
Autoimmune lymphoproliferative syndrome type 43Feb 21, 2021
Autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD1Mar 5, 2021
Autoimmune thyroid disease, susceptibility to, 31Feb 21, 2021
Autoinflammation with arthritis and dyskeratosis1Mar 5, 2021
Autoinflammation, immune dysregulation, and eosinophilia1Oct 2, 2023
Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation9Oct 2, 2023
Autoinflammatory syndrome, familial, Behcet-like2Mar 5, 2021
Autoinflammatory syndrome, familial, X-linked, Behcet-like 21Feb 19, 2023
Autosomal dominant Alport syndrome4Mar 5, 2021
Autosomal dominant Parkinson disease 82Feb 21, 2021
Autosomal dominant Robinow syndrome 12Mar 5, 2021
Autosomal dominant Robinow syndrome 21Feb 21, 2021
Autosomal dominant Robinow syndrome 32Feb 19, 2023
Autosomal dominant centronuclear myopathy7Mar 5, 2021
Autosomal dominant cerebellar ataxia, deafness and narcolepsy2Mar 5, 2021
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures3Mar 5, 2021
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures4Oct 2, 2023
Autosomal dominant deafness - onychodystrophy syndrome1Feb 21, 2021
Autosomal dominant distal renal tubular acidosis1Feb 21, 2021
Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome2Mar 5, 2021
Autosomal dominant hypocalcemia 11Oct 16, 2017
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome16Oct 2, 2023
Autosomal dominant isolated somatotropin deficiency1Feb 21, 2021
Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)1Feb 21, 2021
Autosomal dominant limb-girdle muscular dystrophy type 1F3Feb 19, 2023
Autosomal dominant nocturnal frontal lobe epilepsy 18Feb 19, 2023
Autosomal dominant nocturnal frontal lobe epilepsy 32Mar 5, 2021
Autosomal dominant nocturnal frontal lobe epilepsy 42Feb 19, 2023
Autosomal dominant nocturnal frontal lobe epilepsy 58Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 12Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 117Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 128Feb 19, 2023
Autosomal dominant nonsyndromic hearing loss 131Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 152Feb 19, 2023
Autosomal dominant nonsyndromic hearing loss 173Oct 2, 2023
Autosomal dominant nonsyndromic hearing loss 201Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 231Oct 16, 2017
Autosomal dominant nonsyndromic hearing loss 2A1Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 2B1Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 362Oct 2, 2023
Autosomal dominant nonsyndromic hearing loss 3A4Feb 19, 2023
Autosomal dominant nonsyndromic hearing loss 411Feb 21, 2021
Autosomal dominant nonsyndromic hearing loss 441Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 4A3Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 4B2Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 51Feb 21, 2021
Autosomal dominant nonsyndromic hearing loss 565Feb 19, 2023
Autosomal dominant nonsyndromic hearing loss 62Feb 21, 2021
Autosomal dominant nonsyndromic hearing loss 651Mar 14, 2019
Autosomal dominant nonsyndromic hearing loss 661Oct 2, 2023
Autosomal dominant nonsyndromic hearing loss 681Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 703Mar 5, 2021
Autosomal dominant nonsyndromic hearing loss 91Feb 21, 2021
Autosomal dominant optic atrophy classic form2Feb 21, 2021
Autosomal dominant osteopetrosis 21Mar 12, 2023
Autosomal dominant progressive external ophthalmoplegia1Feb 19, 2023
Autosomal dominant pseudohypoaldosteronism type 11Feb 21, 2021
Autosomal dominant sensory ataxia 11Feb 21, 2021
Autosomal dominant slowed nerve conduction velocity4Mar 5, 2021
Autosomal recessive Alport syndrome10Feb 19, 2023
Autosomal recessive DOPA responsive dystonia51Dec 7, 2023
Autosomal recessive Parkinson disease 141Aug 17, 2015
Autosomal recessive ataxia due to ubiquinone deficiency9Oct 2, 2023
Autosomal recessive ataxia, Beauce type13Oct 2, 2023
Autosomal recessive bestrophinopathy1Feb 21, 2021
Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome14Dec 14, 2023
Autosomal recessive complex spastic paraplegia type 9B3Feb 19, 2023
Autosomal recessive congenital ichthyosis 196Dec 7, 2023
Autosomal recessive congenital ichthyosis 27Mar 12, 2023
Autosomal recessive congenital ichthyosis 32Oct 2, 2023
Autosomal recessive congenital ichthyosis 54Mar 5, 2021
Autosomal recessive congenital ichthyosis 62Mar 5, 2021
Autosomal recessive cutis laxa type 2B4Oct 2, 2023
Autosomal recessive distal spinal muscular atrophy 16Mar 12, 2023
Autosomal recessive early-onset Parkinson disease 233Feb 21, 2021
Autosomal recessive early-onset Parkinson disease 64Feb 21, 2021
Autosomal recessive hypophosphatemic bone disease1Feb 19, 2023
Autosomal recessive inherited pseudoxanthoma elasticum5Mar 5, 2021
Autosomal recessive juvenile Parkinson disease 24Mar 5, 2021
Autosomal recessive limb-girdle muscular dystrophy type 2A14Mar 12, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2B2Feb 23, 2024
Autosomal recessive limb-girdle muscular dystrophy type 2C35Dec 7, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2D59Dec 7, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2E40Dec 7, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2F1Feb 19, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2I2Mar 12, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2J49Oct 2, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2P1Oct 2, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2Q8Feb 19, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2T1Feb 21, 2021
Autosomal recessive limb-girdle muscular dystrophy type 2W1Feb 21, 2021
Autosomal recessive limb-girdle muscular dystrophy type 2Y1Mar 5, 2021
Autosomal recessive limb-girdle muscular dystrophy type R186Feb 19, 2023
Autosomal recessive multiple pterygium syndrome4Oct 2, 2023
Autosomal recessive nonsyndromic hearing loss 1021Mar 5, 2021
Autosomal recessive nonsyndromic hearing loss 1214Oct 2, 2023
Autosomal recessive nonsyndromic hearing loss 151Feb 21, 2021
Autosomal recessive nonsyndromic hearing loss 164Feb 21, 2021
Autosomal recessive nonsyndromic hearing loss 18A56Dec 7, 2023
Autosomal recessive nonsyndromic hearing loss 18B16Feb 19, 2023
Autosomal recessive nonsyndromic hearing loss 1A25Mar 12, 2023
Autosomal recessive nonsyndromic hearing loss 1B16Sep 27, 2019
Autosomal recessive nonsyndromic hearing loss 26Mar 12, 2023
Autosomal recessive nonsyndromic hearing loss 224Feb 19, 2023
Autosomal recessive nonsyndromic hearing loss 23108Dec 7, 2023
Autosomal recessive nonsyndromic hearing loss 251Feb 21, 2021
Autosomal recessive nonsyndromic hearing loss 286Mar 5, 2021
Autosomal recessive nonsyndromic hearing loss 313Feb 19, 2023
Autosomal recessive nonsyndromic hearing loss 301Mar 5, 2021
Autosomal recessive nonsyndromic hearing loss 312Mar 5, 2021
Autosomal recessive nonsyndromic hearing loss 322Feb 21, 2021
Autosomal recessive nonsyndromic hearing loss 353Feb 21, 2021
Autosomal recessive nonsyndromic hearing loss 362Oct 2, 2023
Autosomal recessive nonsyndromic hearing loss 391Feb 19, 2023
Autosomal recessive nonsyndromic hearing loss 4189Dec 14, 2023
Autosomal recessive nonsyndromic hearing loss 421Mar 5, 2021
Autosomal recessive nonsyndromic hearing loss 441Feb 21, 2021
Autosomal recessive nonsyndromic hearing loss 61Mar 5, 2021
Autosomal recessive nonsyndromic hearing loss 611Mar 5, 2021
Autosomal recessive nonsyndromic hearing loss 661Mar 5, 2021
Autosomal recessive nonsyndromic hearing loss 71Feb 21, 2021
Autosomal recessive nonsyndromic hearing loss 7011Oct 2, 2023
Autosomal recessive nonsyndromic hearing loss 778Feb 19, 2023
Autosomal recessive nonsyndromic hearing loss 82Dec 14, 2023
Autosomal recessive nonsyndromic hearing loss 84A1Oct 2, 2023
Autosomal recessive nonsyndromic hearing loss 84B7Mar 5, 2021
Autosomal recessive nonsyndromic hearing loss 861Mar 14, 2019
Autosomal recessive nonsyndromic hearing loss 97Mar 12, 2023
Autosomal recessive nonsyndromic hearing loss 911Mar 5, 2021
Autosomal recessive nonsyndromic hearing loss 97128Dec 7, 2023
Autosomal recessive nonsyndromic hearing loss 983Mar 5, 2021
Autosomal recessive osteopetrosis 194Dec 7, 2023
Autosomal recessive osteopetrosis 42Feb 19, 2023
Autosomal recessive osteopetrosis 71Feb 21, 2021
Autosomal recessive polycystic kidney disease73Sep 27, 2019
Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity2Mar 5, 2021
Autosomal recessive proximal renal tubular acidosis1Feb 21, 2021
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency4Mar 5, 2021
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency3Dec 14, 2023
Autosomal recessive spastic paraplegia type 762Feb 19, 2023
Autosomal recessive spastic paraplegia type 786Feb 19, 2023
Autosomal recessive spinocerebellar ataxia 103Mar 5, 2021
Autosomal recessive spinocerebellar ataxia 111Mar 5, 2021
Autosomal recessive spinocerebellar ataxia 124Mar 14, 2019
Autosomal recessive spinocerebellar ataxia 131Feb 21, 2021
Autosomal recessive spinocerebellar ataxia 142Mar 5, 2021
Autosomal recessive spinocerebellar ataxia 152Feb 21, 2021
Autosomal recessive spinocerebellar ataxia 161Feb 21, 2021
Autosomal recessive spinocerebellar ataxia 183Feb 19, 2023
Autosomal recessive spinocerebellar ataxia 25Mar 5, 2021
Autosomal recessive spinocerebellar ataxia 209Dec 6, 2021
Avascular necrosis of femoral head, primary, 11Feb 21, 2021
Ayme-Gripp syndrome1Feb 21, 2021
B-cell immunodeficiency, distal limb anomalies, and urogenital malformations2Feb 19, 2023
B4GALT1-congenital disorder of glycosylation2Mar 5, 2021
BAP1-related tumor predisposition syndrome143Dec 7, 2023
BCL11A-related BAFopathy3Jul 1, 2021
BENTA disease7Mar 5, 2021
BNAR syndrome3Feb 21, 2021
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 203Dec 14, 2023
BSN related epilepsy2Dec 14, 2023
Baller-Gerold syndrome9Dec 7, 2023
Bamforth-Lazarus syndrome3Mar 5, 2021
Band heterotopia of brain2Mar 5, 2021
Baraitser-Winter syndrome 17Mar 12, 2023
Baraitser-winter syndrome 23Feb 21, 2021
Baralle-Macken syndrome3Oct 2, 2023
Barber-Say syndrome1Mar 5, 2021
Bardet-Biedl syndrome 157Dec 7, 2023
Bardet-Biedl syndrome 1083Dec 7, 2023
Bardet-Biedl syndrome 112Mar 5, 2021
Bardet-Biedl syndrome 1265Dec 7, 2023
Bardet-Biedl syndrome 1349Dec 7, 2023
Bardet-Biedl syndrome 14302Dec 7, 2023
Bardet-Biedl syndrome 163Feb 21, 2021
Bardet-Biedl syndrome 281Dec 7, 2023
Bardet-Biedl syndrome 221Feb 21, 2021
Bardet-Biedl syndrome 31Feb 21, 2021
Bardet-Biedl syndrome 455Dec 7, 2023
Bardet-Biedl syndrome 52Mar 5, 2021
Bardet-Biedl syndrome 640Dec 7, 2023
Bardet-Biedl syndrome 757Dec 7, 2023
Bardet-Biedl syndrome 941Dec 7, 2023
Bartsocas-Papas syndrome 13Mar 5, 2021
Bartter disease type 17Oct 2, 2023
Bartter disease type 4A1Feb 21, 2021
Bartter disease type 4B2Oct 2, 2023
Bartter disease type 51Oct 2, 2023
Basal cell carcinoma, susceptibility to, 1100Dec 7, 2023
Basal ganglia calcification, idiopathic, 51Feb 21, 2021
Basal laminar drusen2Mar 5, 2021
Basilicata-Akhtar syndrome1Feb 19, 2023
Beaded hair1Oct 16, 2017
Beck-Fahrner syndrome2Feb 19, 2023
Becker muscular dystrophy31Dec 7, 2023
Beckwith-Wiedemann syndrome34Dec 7, 2023
Benign familial hematuria1Mar 5, 2021
Benign hereditary chorea1Mar 14, 2019
Benign recurrent intrahepatic cholestasis type 146Dec 7, 2023
Benign recurrent intrahepatic cholestasis type 297Dec 7, 2023
Bernard Soulier syndrome2Mar 5, 2021
Beta-D-mannosidosis4Mar 5, 2021
Beta-hydroxyisobutyryl-CoA deacylase deficiency5Feb 19, 2023
Beta-thalassemia HBB/LCRB2Mar 12, 2023
Beta-thalassemia-X-linked thrombocytopenia syndrome1Feb 21, 2021
Bethlem myopathy 1A10Feb 19, 2023
Bethlem myopathy 26Dec 14, 2023
Bifunctional peroxisomal enzyme deficiency65Dec 7, 2023
Bilateral frontoparietal polymicrogyria2Feb 21, 2021
Bilateral microtia-deafness-cleft palate syndrome1Mar 5, 2021
Bilateral parasagittal parieto-occipital polymicrogyria3Dec 14, 2023
Bilateral sensorineural hearing impairment1Nov 14, 2016
Bile acid malabsorption, primary, 13Feb 21, 2021
Biotin-responsive basal ganglia disease5Feb 19, 2023
Biotinidase deficiency106Dec 14, 2023
Birk-Barel syndrome2Mar 12, 2023
Birt-Hogg-Dube syndrome83Dec 14, 2023
Blau syndrome2Mar 5, 2021
Bleeding disorder, platelet-type, 241Feb 19, 2023
Blepharocheilodontic syndrome 14Feb 19, 2023
Blepharocheilodontic syndrome 22Oct 2, 2023
Blepharophimosis - intellectual disability syndrome, MKB type1Feb 21, 2021
Blepharophimosis - intellectual disability syndrome, SBBYS type2Feb 21, 2021
Blepharophimosis-impaired intellectual development syndrome3Oct 2, 2023
Bloom syndrome122Dec 7, 2023
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency1Mar 5, 2021
Bohring-Opitz syndrome10Feb 19, 2023
Bone fragility with contractures, arterial rupture, and deafness1Mar 5, 2021
Bone marrow failure syndrome 33Mar 5, 2021
Bone marrow failure syndrome 42Feb 19, 2023
Bone marrow failure syndrome 51Feb 10, 2021
Bone mineral density quantitative trait locus 184Feb 19, 2023
Borjeson-Forssman-Lehmann syndrome3Feb 19, 2023
Bosch-Boonstra-Schaaf optic atrophy syndrome2Feb 19, 2023
Brachycephaly, trichomegaly, and developmental delay1Feb 21, 2021
Brachydactyly type B11Feb 21, 2021
Brachydactyly type D1Mar 14, 2019
Brachydactyly type E12Dec 14, 2023
Brachydactyly-syndactyly syndrome1Mar 5, 2021
Brachyolmia-amelogenesis imperfecta syndrome3Mar 5, 2021
Brachyrachia (short spine dysplasia)1Feb 21, 2021
Brain abnormalities, neurodegeneration, and dysosteosclerosis3Feb 19, 2023
Brain imaging abnormality12Jul 17, 2021
Brain small vessel disease 1 with or without ocular anomalies15Oct 2, 2023
Brain-lung-thyroid syndrome3Feb 21, 2021
Branched-chain keto acid dehydrogenase kinase deficiency3Mar 5, 2021
Branchiooculofacial syndrome2Mar 5, 2021
Branchiootic syndrome 32Oct 2, 2023
Branchiootorenal syndrome 11Feb 19, 2023
Breast-ovarian cancer, familial, susceptibility to, 1517Dec 7, 2023
Breast-ovarian cancer, familial, susceptibility to, 228Dec 14, 2023
Breast-ovarian cancer, familial, susceptibility to, 3162Dec 7, 2023
Breast-ovarian cancer, familial, susceptibility to, 4130Dec 7, 2023
Brittle cornea syndrome 113Mar 5, 2021
Brittle cornea syndrome 21Feb 19, 2023
Brody myopathy3Mar 5, 2021
Bronchiectasis with or without elevated sweat chloride 1357Dec 7, 2023
Bronchiectasis with or without elevated sweat chloride 33Mar 5, 2021
Brooke-Spiegler syndrome1Dec 6, 2021
Brown-Vialetto-van Laere syndrome 26Feb 19, 2023
Bruck syndrome 13Feb 21, 2021
Brugada syndrome 14Oct 2, 2023
Brugada syndrome 32Feb 21, 2021
Brugada syndrome 42Feb 19, 2023
Brugada syndrome 51Feb 21, 2021
Brugada syndrome 81Feb 19, 2023
Brugada syndrome 91Dec 14, 2023
Brunner syndrome1Mar 5, 2021
Bryant-Li-Bhoj neurodevelopmental syndrome 21Feb 19, 2023
Bullous ichthyosiform erythroderma2Feb 19, 2023
C syndrome3Feb 21, 2021
C1Q deficiency1Feb 21, 2021
CARASIL syndrome1Feb 21, 2021
CASR-related calcium metabolism disorders1Oct 2, 2023
CATARACTS, SPASTIC PARAPARESIS, AND SPEECH DELAY1Oct 2, 2023
CBL-related disorder6Oct 2, 2023
CCDC115-CDG1Mar 5, 2021
CEBALID syndrome4Oct 2, 2023
CEDNIK syndrome1Feb 21, 2021
CEP290-Related Disorders2Feb 19, 2023
CFHR5 deficiency2Feb 21, 2021
CHARGE association30Oct 2, 2023
CHIME syndrome2Oct 2, 2023
CK syndrome1Feb 19, 2023
COACH syndrome 117Mar 5, 2021
CODAS syndrome7Feb 19, 2023
COG1 congenital disorder of glycosylation7Mar 5, 2021
COG4-congenital disorder of glycosylation2Feb 19, 2023
COG5-congenital disorder of glycosylation4Mar 5, 2021
COG6-ongenital disorder of glycosylation7Feb 19, 2023
COG7 congenital disorder of glycosylation10Mar 5, 2021
COG8-congenital disorder of glycosylation3Mar 5, 2021
Café-au-lait macules with pulmonary stenosis2Mar 5, 2021
Camptodactyly-tall stature-scoliosis-hearing loss syndrome1Mar 14, 2019
Camptomelic dysplasia3Oct 2, 2023
Candidiasis, familial, 81Mar 5, 2021
Capillary malformation-arteriovenous malformation 13Mar 5, 2021
Capillary malformation-arteriovenous malformation 21Oct 2, 2023
Carcinoma of pancreas3Feb 10, 2021
Cardiac anomalies - developmental delay - facial dysmorphism syndrome14Oct 2, 2023
Cardiac arrhythmia4Sep 3, 2015
Cardiac arrhythmia, ankyrin-B-related5Mar 5, 2021
Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies3Feb 19, 2023
Cardiac valvular defect, developmental9Oct 2, 2023
Cardiac valvular dysplasia, X-linked5Feb 19, 2023
Cardiac, facial, and digital anomalies with developmental delay3Feb 19, 2023
Cardiac-urogenital syndrome5Oct 2, 2023
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 116Dec 7, 2023
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 22Mar 5, 2021
Cardiofaciocutaneous syndrome 13Mar 5, 2021
Cardiofaciocutaneous syndrome 22Mar 14, 2019
Cardiofaciocutaneous syndrome 32Oct 2, 2023
Cardiofaciocutaneous syndrome 43Mar 5, 2021
Cardiomyopathy7Jun 19, 2015
Cardiomyopathy, dilated, 2c1Feb 21, 2021
Cardiomyopathy, familial hypertrophic 277Oct 2, 2023
Cardiomyopathy, familial hypertrophic, 281Oct 2, 2023
Cardiospondylocarpofacial syndrome1Feb 21, 2021
Carey-Fineman-Ziter syndrome 11Dec 14, 2023
Carney complex, type 11Dec 6, 2021
Carney-Stratakis syndrome1Feb 21, 2021
Carnitine acylcarnitine translocase deficiency29Dec 7, 2023
Carnitine palmitoyl transferase 1A deficiency46Dec 7, 2023
Carnitine palmitoyl transferase II deficiency, neonatal form5Sep 27, 2019
Carnitine palmitoyl transferase II deficiency, severe infantile form11Mar 5, 2021
Cat eye syndrome1Apr 1, 2019
Cataract 1 multiple types1Feb 21, 2021
Cataract 10 multiple types1Mar 5, 2021
Cataract 11 multiple types1Oct 2, 2023
Cataract 12 multiple types1Mar 5, 2021
Cataract 181Feb 21, 2021
Cataract 19 multiple types1Feb 21, 2021
Cataract 2, multiple types1Mar 5, 2021
Cataract 3 multiple types1Feb 19, 2023
Cataract 361Feb 21, 2021
Cataract 4 multiple types1Mar 14, 2019
Cataract 402Feb 21, 2021
Cataract 431Mar 5, 2021
Cataract 442Mar 5, 2021
Cataract 451Mar 5, 2021
Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome3Mar 5, 2021
Catecholaminergic polymorphic ventricular tachycardia 19Oct 2, 2023
Catecholaminergic polymorphic ventricular tachycardia 22Feb 19, 2023
Catecholaminergic polymorphic ventricular tachycardia 32Feb 19, 2023
Catecholaminergic polymorphic ventricular tachycardia 52Mar 12, 2023
Catifa syndrome2Feb 19, 2023
Cayman type cerebellar ataxia1Feb 21, 2021
Cenani-Lenz syndactyly syndrome1Mar 5, 2021
Central core myopathy28Mar 12, 2023
Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease1Oct 2, 2023
Cerebellar ataxia1Aug 17, 2015
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome2Feb 19, 2023
Cerebellar ataxia, brain abnormalities, and cardiac conduction defects2Feb 19, 2023
Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 16Mar 5, 2021
Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 214Feb 19, 2023
Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 44Mar 5, 2021
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome3Feb 21, 2021
Cerebellar atrophy with seizures and variable developmental delay1Feb 21, 2021
Cerebellar atrophy, visual impairment, and psychomotor retardation;13Oct 2, 2023
Cerebellar dysfunction with variable cognitive and behavioral abnormalities12Oct 2, 2023
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome1Oct 2, 2023
Cerebellar-facial-dental syndrome3Feb 21, 2021
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 15Oct 2, 2023
Cerebral cavernous malformation3Oct 2, 2023
Cerebral cavernous malformation 22Mar 5, 2021
Cerebral cavernous malformation 33Feb 19, 2023
Cerebral cavernous malformation 41Oct 2, 2023
Cerebral folate transport deficiency1Feb 21, 2021
Cerebral palsy, spastic quadriplegic, 25Oct 2, 2023
Cerebral palsy, spastic quadriplegic, 33Feb 21, 2021
Cerebrooculofacioskeletal syndrome 17Mar 5, 2021
Cerebrooculofacioskeletal syndrome 291Dec 7, 2023
Cerebrooculofacioskeletal syndrome 316Dec 6, 2021
Cerebrooculofacioskeletal syndrome 41Feb 19, 2023
Cerebroretinal microangiopathy with calcifications and cysts 18Dec 14, 2023
Cerebroretinal microangiopathy with calcifications and cysts 21Feb 21, 2021
Ceroid lipofuscinosis, neuronal, 6A3Oct 2, 2023
Ceroid lipofuscinosis, neuronal, 6B (Kufs type)1Oct 2, 2023
Channelopathy-associated congenital insensitivity to pain, autosomal recessive2Mar 12, 2023
Char syndrome3Feb 19, 2023
Charcot-Marie-Tooth disease X-linked dominant 12Feb 21, 2021
Charcot-Marie-Tooth disease axonal type 2C1Feb 19, 2023
Charcot-Marie-Tooth disease axonal type 2CC2Mar 5, 2021
Charcot-Marie-Tooth disease axonal type 2K1Mar 5, 2021
Charcot-Marie-Tooth disease axonal type 2N5Oct 2, 2023
Charcot-Marie-Tooth disease axonal type 2O5Oct 2, 2023
Charcot-Marie-Tooth disease axonal type 2P2Mar 5, 2021
Charcot-Marie-Tooth disease axonal type 2Q3Mar 5, 2021
Charcot-Marie-Tooth disease axonal type 2S5Mar 5, 2021
Charcot-Marie-Tooth disease axonal type 2T2Feb 19, 2023
Charcot-Marie-Tooth disease axonal type 2U2Mar 5, 2021
Charcot-Marie-Tooth disease axonal type 2X2Feb 21, 2021
Charcot-Marie-Tooth disease axonal type 2Z5Oct 2, 2023
Charcot-Marie-Tooth disease dominant intermediate C2Feb 21, 2021
Charcot-Marie-Tooth disease dominant intermediate D1Feb 21, 2021
Charcot-Marie-Tooth disease dominant intermediate F1Mar 5, 2021
Charcot-Marie-Tooth disease recessive intermediate B2Feb 19, 2023
Charcot-Marie-Tooth disease recessive intermediate C6Feb 21, 2021
Charcot-Marie-Tooth disease recessive intermediate D2Oct 2, 2023
Charcot-Marie-Tooth disease type 1B1Feb 21, 2021
Charcot-Marie-Tooth disease type 2A29Oct 2, 2023
Charcot-Marie-Tooth disease type 2B11Feb 19, 2023
Charcot-Marie-Tooth disease type 2B21Feb 21, 2021
Charcot-Marie-Tooth disease type 2D3Mar 12, 2023
Charcot-Marie-Tooth disease type 2E1Feb 19, 2023
Charcot-Marie-Tooth disease type 2I1Feb 19, 2023
Charcot-Marie-Tooth disease type 2R1Feb 21, 2021
Charcot-Marie-Tooth disease type 2Y1Feb 19, 2023
Charcot-Marie-Tooth disease type 4A2Feb 21, 2021
Charcot-Marie-Tooth disease type 4B12Feb 21, 2021
Charcot-Marie-Tooth disease type 4B26Mar 5, 2021
Charcot-Marie-Tooth disease type 4B36Mar 5, 2021
Charcot-Marie-Tooth disease type 4C8Feb 19, 2023
Charcot-Marie-Tooth disease type 4D2Mar 5, 2021
Charcot-Marie-Tooth disease type 4E1Nov 14, 2016
Charcot-Marie-Tooth disease type 4F11Oct 2, 2023
Charcot-Marie-Tooth disease type 4G1Feb 21, 2021
Charcot-Marie-Tooth disease type 4J4Feb 19, 2023
Charcot-Marie-Tooth disease type 4K1Mar 5, 2021
Charcot-Marie-Tooth disease, axonal, IIa 2II1Oct 2, 2023
Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;7Oct 2, 2023
Charcot-Marie-Tooth disease, axonal, type 2EE34Dec 7, 2023
Charcot-Marie-Tooth disease, type IA3Apr 1, 2019
Charcot-marie-tooth disease, axonal, type 2DD1Feb 21, 2021
Charlevoix-Saguenay spastic ataxia204Dec 7, 2023
Chilblain lupus 12Mar 14, 2019
Child syndrome1Feb 19, 2023
Childhood apraxia of speech3Mar 5, 2021
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency3Feb 21, 2021
Childhood hypophosphatasia3Mar 5, 2021
Childhood onset GLUT1 deficiency syndrome 23Mar 5, 2021
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder1Feb 21, 2021
Chilton-Okur-Chung neurodevelopmental syndrome1Feb 19, 2023
Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome1Feb 21, 2021
Cholestanol storage disease79Dec 7, 2023
Cholestasis, intrahepatic, of pregnancy, 36Oct 2, 2023
Cholestasis, progressive familial intrahepatic, 44Mar 5, 2021
Cholestasis, progressive familial intrahepatic, 61Feb 19, 2023
Cholestasis, progressive familial intrahepatic, 7, with or without hearing loss1Feb 19, 2023
Cholestasis, progressive familial intrahepatic, 81Feb 19, 2023
Cholestasis-pigmentary retinopathy-cleft palate syndrome3Dec 14, 2023
Chondrodysplasia with joint dislocations, gPAPP type2Feb 19, 2023
Chondrosarcoma67Dec 7, 2023
Chopra-Amiel-Gordon syndrome1Feb 19, 2023
Chorea-acanthocytosis7Mar 5, 2021
Christianson syndrome2Mar 5, 2021
Chromosome 16p11.2 duplication syndrome5Apr 1, 2019
Chromosome 16p12.1 deletion syndrome, 520kb6Apr 1, 2019
Chromosome 16p13.3 duplication syndrome1Apr 1, 2019
Chromosome 17P13.3, telomeric, duplication syndrome2Apr 1, 2019
Chromosome 17q11.2 deletion syndrome, 1.4Mb1Mar 5, 2021
Chromosome 17q12 deletion syndrome2Apr 1, 2019
Chromosome 17q12 duplication syndrome4Apr 1, 2019
Chromosome 1p32-p31 deletion syndrome2Feb 21, 2021
Chromosome 1p36 deletion syndrome3Apr 1, 2019
Chromosome 1q21.1 deletion syndrome3Apr 1, 2019
Chromosome 1q21.1 duplication syndrome4Apr 1, 2019
Chromosome 22q11.2 deletion syndrome, distal1Apr 1, 2019
Chromosome 22q11.2 microduplication syndrome12Apr 1, 2019
Chromosome 2q32-q33 deletion syndrome7Dec 14, 2023
Chromosome 2q37 deletion syndrome3Apr 1, 2019
Chronic infantile neurological, cutaneous and articular syndrome1Feb 21, 2021
Chuvash polycythemia61Dec 7, 2023
Chédiak-Higashi syndrome65Dec 7, 2023
Ciliary dyskinesia, primary, 3713Dec 14, 2023
Ciliary dyskinesia, primary, 391Feb 19, 2023
Ciliary dyskinesia, primary, 408Oct 2, 2023
Ciliary dyskinesia, primary, 49, without situs inversus1Oct 2, 2023
Cirrhosis, familial2Feb 21, 2021
Citrullinemia type I96Dec 7, 2023
Citrullinemia, type II, adult-onset83Dec 7, 2023
Clark-Baraitser syndrome9Oct 2, 2023
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency3Oct 2, 2023
Classic homocystinuria98Dec 7, 2023
Cleft lip/palate-ectodermal dysplasia syndrome1Feb 21, 2021
Cleidocranial dysostosis2Mar 5, 2021
Clubfoot1Mar 5, 2021
Cobalamin C disease91Feb 2, 2024
Cobblestone lissencephaly without muscular or ocular involvement9Oct 2, 2023
Cockayne syndrome type 23Oct 16, 2017
Coenzyme Q10 deficiency, primary, 15Mar 5, 2021
Coenzyme Q10 deficiency, primary, 35Oct 2, 2023
Coenzyme q10 deficiency, primary, 91Oct 2, 2023
Coffin-Lowry syndrome1Feb 21, 2021
Coffin-Siris syndrome 140Dec 14, 2023
Coffin-Siris syndrome 101Feb 21, 2021
Coffin-Siris syndrome 124Oct 2, 2023
Coffin-Siris syndrome 53Oct 2, 2023
Coffin-Siris syndrome 68Dec 14, 2023
Coffin-Siris syndrome 72Feb 19, 2023
Coffin-Siris syndrome 86Feb 19, 2023
Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome3Mar 5, 2021
Cognitive impairment with or without cerebellar ataxia13Oct 2, 2023
Cohen syndrome27Oct 2, 2023
Cole-Carpenter syndrome 11Mar 5, 2021
Cole-Carpenter syndrome 21Mar 5, 2021
Coloboma of optic nerve1Mar 5, 2021
Coloboma, ocular, autosomal recessive1Mar 5, 2021
Colobomatous microphthalmia-rhizomelic dysplasia syndrome1Mar 5, 2021
Colorectal cancer182Dec 7, 2023
Colorectal cancer, hereditary nonpolyposis, type 2257Dec 7, 2023
Colorectal cancer, hereditary nonpolyposis, type 71Feb 10, 2021
Colorectal cancer, susceptibility to, 1107Dec 7, 2023
Colorectal cancer, susceptibility to, 1069Dec 7, 2023
Colorectal cancer, susceptibility to, 1267Dec 7, 2023
Combined PSAP deficiency7Oct 2, 2023
Combined deficiency of sialidase AND beta galactosidase1Feb 21, 2021
Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia3Mar 12, 2023
Combined immunodeficiency due to CD3gamma deficiency1Feb 21, 2021
Combined immunodeficiency due to DOCK8 deficiency22Mar 5, 2021
Combined immunodeficiency due to GINS1 deficiency1Mar 5, 2021
Combined immunodeficiency due to LRBA deficiency20Dec 14, 2023
Combined immunodeficiency due to MALT1 deficiency6Mar 5, 2021
Combined immunodeficiency due to ORAI1 deficiency2Mar 5, 2021
Combined immunodeficiency due to STIM1 deficiency1Mar 14, 2019
Combined immunodeficiency due to ZAP70 deficiency1Feb 21, 2021
Combined immunodeficiency due to partial RAG1 deficiency77Dec 7, 2023
Combined immunodeficiency with skin granulomas34Dec 7, 2023
Combined immunodeficiency, X-linked1Feb 21, 2021
Combined malonic and methylmalonic acidemia100Dec 7, 2023
Combined oxidative phosphorylation defect type 117Mar 12, 2023
Combined oxidative phosphorylation defect type 1311Mar 5, 2021
Combined oxidative phosphorylation defect type 149Oct 2, 2023
Combined oxidative phosphorylation defect type 157Feb 21, 2021
Combined oxidative phosphorylation defect type 175Feb 19, 2023
Combined oxidative phosphorylation defect type 21Feb 19, 2023
Combined oxidative phosphorylation defect type 2015Oct 2, 2023
Combined oxidative phosphorylation defect type 215Mar 5, 2021
Combined oxidative phosphorylation defect type 232Mar 5, 2021
Combined oxidative phosphorylation defect type 246Mar 5, 2021
Combined oxidative phosphorylation defect type 253Mar 5, 2021
Combined oxidative phosphorylation defect type 262Mar 5, 2021
Combined oxidative phosphorylation defect type 279Oct 2, 2023
Combined oxidative phosphorylation defect type 43Mar 5, 2021
Combined oxidative phosphorylation defect type 812Oct 2, 2023
Combined oxidative phosphorylation defect type 92Oct 2, 2023
Combined oxidative phosphorylation deficiency 191Feb 21, 2021
Combined oxidative phosphorylation deficiency 221Mar 5, 2021
Combined oxidative phosphorylation deficiency 291Feb 21, 2021
Combined oxidative phosphorylation deficiency 322Feb 19, 2023
Combined oxidative phosphorylation deficiency 342Feb 21, 2021
Combined oxidative phosphorylation deficiency 353Feb 19, 2023
Combined oxidative phosphorylation deficiency 362Feb 21, 2021
Combined oxidative phosphorylation deficiency 393Feb 19, 2023
Combined oxidative phosphorylation deficiency 441Feb 19, 2023
Combined oxidative phosphorylation deficiency 513Feb 19, 2023
Combined oxidative phosphorylation deficiency 5511Dec 14, 2023
Complement component 2 deficiency1Mar 5, 2021
Complement component 3 deficiency3Feb 19, 2023
Complement component 4a deficiency2Mar 5, 2021
Complement component 4b deficiency1Mar 5, 2021
Complement component 5 deficiency5Feb 19, 2023
Complement component 6 deficiency2Dec 14, 2023
Complement component 7 deficiency2Mar 5, 2021
Complement component 9 deficiency1Mar 5, 2021
Complex cortical dysplasia with other brain malformations 15Oct 2, 2023
Complex cortical dysplasia with other brain malformations 23Feb 19, 2023
Complex cortical dysplasia with other brain malformations 32Feb 19, 2023
Complex cortical dysplasia with other brain malformations 54Feb 19, 2023
Complex cortical dysplasia with other brain malformations 63Oct 2, 2023
Complex cortical dysplasia with other brain malformations 72Feb 21, 2021
Compton-North congenital myopathy1Feb 21, 2021
Cone dystrophy 31Feb 21, 2021
Cone dystrophy with supernormal rod response1Mar 5, 2021
Cone-rod dystrophy 121Feb 21, 2021
Cone-rod dystrophy 133Mar 5, 2021
Cone-rod dystrophy 33Mar 5, 2021
Cone-rod dystrophy 51Mar 5, 2021
Cone-rod dystrophy 72Feb 19, 2023
Cone-rod dystrophy and hearing loss 11Feb 21, 2021
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency1Feb 21, 2021
Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency1Mar 5, 2021
Congenital amegakaryocytic thrombocytopenia4Feb 21, 2021
Congenital anomalies of kidney and urinary tract 11Mar 5, 2021
Congenital anomalies of kidney and urinary tract 21Feb 19, 2023
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay2Oct 2, 2023
Congenital bilateral aplasia of vas deferens from CFTR mutation187Mar 12, 2023
Congenital bile acid synthesis defect 14Oct 2, 2023
Congenital bile acid synthesis defect 23Feb 21, 2021
Congenital bile acid synthesis defect 34Mar 5, 2021
Congenital bile acid synthesis defect 61Mar 5, 2021
Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome3Mar 5, 2021
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome2Oct 16, 2017
Congenital central hypoventilation5Feb 21, 2021
Congenital cerebellar hypoplasia1Feb 19, 2023
Congenital contractural arachnodactyly5Mar 5, 2021
Congenital contractures of the limbs and face, hypotonia, and developmental delay6Oct 2, 2023
Congenital defect of folate absorption2Feb 21, 2021
Congenital diarrhea 61Mar 5, 2021
Congenital diarrhea 7 with exudative enteropathy3Feb 21, 2021
Congenital disorder of deglycosylation5Mar 5, 2021
Congenital disorder of deglycosylation 12Dec 14, 2023
Congenital disorder of deglycosylation 21Oct 2, 2023
Congenital disorder of glycosylation type 1E2Feb 21, 2021
Congenital disorder of glycosylation type Ir2Mar 5, 2021
Congenital disorder of glycosylation with defective fucosylation 12Feb 19, 2023
Congenital disorder of glycosylation with defective fucosylation 25Feb 19, 2023
Congenital disorder of glycosylation, type 2v2Oct 2, 2023
Congenital disorder of glycosylation, type IAA2Mar 5, 2021
Congenital disorder of glycosylation, type ICC1Oct 2, 2023
Congenital disorder of glycosylation, type IIq2Feb 21, 2021
Congenital disorder of glycosylation, type Iw, autosomal dominant1Oct 2, 2023
Congenital disorder of glycosylation, type iit1Feb 19, 2023
Congenital dyserythropoietic anemia, type II1Feb 21, 2021
Congenital dyserythropoietic anemia, type III1Oct 2, 2023
Congenital factor VII deficiency1Oct 2, 2023
Congenital generalized lipodystrophy type 12Nov 14, 2016
Congenital generalized lipodystrophy type 22Oct 2, 2023
Congenital glucose-galactose malabsorption5Feb 19, 2023
Congenital heart defects and ectodermal dysplasia5Mar 5, 2021
Congenital heart defects and skeletal malformations syndrome6Feb 19, 2023
Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder16Oct 2, 2023
Congenital heart defects, multiple types, 27Feb 19, 2023
Congenital heart defects, multiple types, 41Feb 19, 2023
Congenital heart defects, multiple types, 51Feb 21, 2021
Congenital heart defects, multiple types, 62Mar 5, 2021
Congenital heart disease2Jan 10, 2017
Congenital hyperammonemia, type I10Dec 14, 2023
Congenital hypotonia, epilepsy, developmental delay, and digital anomalies1Oct 2, 2023
Congenital hypotrichosis with juvenile macular dystrophy1Feb 19, 2023
Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome2Oct 16, 2017
Congenital isolated adrenocorticotropic hormone deficiency1Oct 16, 2017
Congenital lactase deficiency1Mar 5, 2021
Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type86Dec 7, 2023
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome3Mar 5, 2021
Congenital microvillous atrophy2Mar 5, 2021
Congenital multicore myopathy with external ophthalmoplegia10Feb 21, 2021
Congenital muscular dystrophy due to LMNA mutation3Feb 21, 2021
Congenital muscular dystrophy due to integrin alpha-7 deficiency7Mar 5, 2021
Congenital muscular dystrophy with cataracts and intellectual disability2Mar 5, 2021
Congenital muscular dystrophy with intellectual disability and severe epilepsy1Feb 21, 2021
Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome1Feb 21, 2021
Congenital muscular hypertrophy-cerebral syndrome22Oct 2, 2023
Congenital myasthenic syndrome 1011Mar 12, 2023
Congenital myasthenic syndrome 114Mar 12, 2023
Congenital myasthenic syndrome 122Mar 5, 2021
Congenital myasthenic syndrome 166Dec 14, 2023
Congenital myasthenic syndrome 193Mar 5, 2021
Congenital myasthenic syndrome 201Feb 19, 2023
Congenital myasthenic syndrome 214Mar 5, 2021
Congenital myasthenic syndrome 2A1Feb 19, 2023
Congenital myasthenic syndrome 3A3Mar 5, 2021
Congenital myasthenic syndrome 3C1Feb 19, 2023
Congenital myasthenic syndrome 4A109Dec 7, 2023
Congenital myasthenic syndrome 4B5Feb 21, 2021
Congenital myasthenic syndrome 4C8Sep 27, 2019
Congenital myasthenic syndrome 548Dec 7, 2023
Congenital myasthenic syndrome 71Feb 21, 2021
Congenital myasthenic syndrome 816Oct 2, 2023
Congenital myasthenic syndrome 95Dec 14, 2023
Congenital myopathy 231Feb 21, 2021
Congenital myopathy 4B, autosomal recessive2Feb 21, 2021
Congenital myopathy with fiber type disproportion5Feb 21, 2021
Congenital myopathy with internal nuclei and atypical cores1Mar 5, 2021
Congenital myotonia, autosomal dominant form4Mar 5, 2021
Congenital myotonia, autosomal recessive form4Mar 12, 2023
Congenital neutropenia-myelofibrosis-nephromegaly syndrome3Feb 21, 2021
Congenital nongoitrous hypothryoidism 61Mar 12, 2023
Congenital nonprogressive myopathy with Moebius and Robin sequences2Feb 21, 2021
Congenital plasminogen activator inhibitor type 1 deficiency1Mar 5, 2021
Congenital prothrombin deficiency2Mar 5, 2021
Congenital secretory diarrhea, chloride type1Feb 21, 2021
Congenital secretory sodium diarrhea 31Feb 21, 2021
Congenital secretory sodium diarrhea 81Mar 5, 2021
Congenital sensory neuropathy with selective loss of small myelinated fibers3Mar 5, 2021
Conotruncal heart malformations2Mar 5, 2021
Corneal dystrophy, Fuchs endothelial, 41Feb 21, 2021
Corneal dystrophy, Fuchs endothelial, 61Mar 5, 2021
Cornelia de Lange syndrome 116Oct 2, 2023
Cornelia de Lange syndrome 35Feb 21, 2021
Cornelia de Lange syndrome 44Oct 2, 2023
Cornelia de Lange syndrome 511Feb 19, 2023
Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome2Feb 21, 2021
Cortical dysplasia, complex, with other brain malformations 102Feb 19, 2023
Cortical dysplasia, complex, with other brain malformations 112Dec 14, 2023
Cortical dysplasia, complex, with other brain malformations 92Oct 2, 2023
Cortical dysplasia-focal epilepsy syndrome17Mar 5, 2021
Corticosteroid-binding globulin deficiency2Feb 21, 2021
Cortisone reductase deficiency 11Feb 21, 2021
Costello syndrome10Oct 2, 2023
Cowden syndrome 18Mar 5, 2021
Cowden syndrome 54Dec 14, 2023
Cowden syndrome 61Mar 5, 2021
Cowden syndrome 73Mar 5, 2021
Cranioectodermal dysplasia 11Feb 21, 2021
Cranioectodermal dysplasia 27Oct 2, 2023
Craniofacial dysplasia - osteopenia syndrome4Mar 5, 2021
Craniofacial-deafness-hand syndrome1Feb 21, 2021
Craniolenticulosutural dysplasia1Mar 5, 2021
Craniosynostosis 42Feb 21, 2021
Creatine transporter deficiency5Dec 7, 2023
Crigler-Najjar syndrome type 11Oct 7, 2022
Crouzon syndrome1Nov 23, 2018
Crouzon syndrome-acanthosis nigricans syndrome2Mar 14, 2019
Cryptosporidiosis-chronic cholangitis-liver disease syndrome3Mar 5, 2021
Curry-Hall syndrome3Mar 5, 2021
Cutis laxa with osteodystrophy3Feb 19, 2023
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies6Oct 2, 2023
Cutis laxa, X-linked6Oct 2, 2023
Cutis laxa, autosomal dominant 12Mar 5, 2021
Cutis laxa, autosomal dominant 23Mar 5, 2021
Cutis laxa, autosomal dominant 34Mar 12, 2023
Cutis laxa, autosomal recessive, type 1A1Mar 14, 2019
Cutis laxa, autosomal recessive, type 1B1Feb 21, 2021
Cyclical neutropenia1Mar 5, 2021
Cystathioninuria1Oct 2, 2023
Cystic fibrosis212Dec 14, 2023
Cystinuria2Dec 14, 2023
D-2-hydroxyglutaric aciduria 19Dec 14, 2023
D-2-hydroxyglutaric aciduria 23Feb 21, 2021
D-Glyceric aciduria4Mar 5, 2021
DDX41-related hematologic malignancy predisposition syndrome69Dec 7, 2023
DICER1-related tumor predisposition2Feb 10, 2021
DK1-congenital disorder of glycosylation1Mar 5, 2021
DOCK2 deficiency11Mar 5, 2021
DOORS syndrome3Feb 21, 2021
DPAGT1-congenital disorder of glycosylation2Mar 5, 2021
DYRK1A-related intellectual disability syndrome9Mar 5, 2021
Dalmatian hypouricemia1Feb 21, 2021
Danon disease4Oct 2, 2023
DeSanto-Shinawi syndrome due to WAC point mutation3Oct 2, 2023
Deafness dystonia syndrome1Oct 2, 2023
Deafness, autosomal dominant 39, with dentinogenesis imperfecta 12Mar 5, 2021
Deafness-encephaloneuropathy-obesity-valvulopathy syndrome2Mar 5, 2021
Deafness-infertility syndrome1Feb 21, 2021
Deafness-lymphedema-leukemia syndrome1Feb 21, 2021
Deficiency of 2-methylbutyryl-CoA dehydrogenase7Mar 12, 2023
Deficiency of 3-hydroxyacyl-CoA dehydrogenase11Dec 7, 2023
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase96Dec 14, 2023
Deficiency of acetyl-CoA acetyltransferase63Dec 7, 2023
Deficiency of alpha-mannosidase86Mar 15, 2024
Deficiency of aromatic-L-amino-acid decarboxylase2Feb 19, 2023
Deficiency of beta-ureidopropionase4Mar 5, 2021
Deficiency of butyryl-CoA dehydrogenase3Feb 19, 2023
Deficiency of galactokinase31Dec 7, 2023
Deficiency of guanidinoacetate methyltransferase46Dec 7, 2023
Deficiency of hydroxymethylglutaryl-CoA lyase30Dec 7, 2023
Deficiency of iodide peroxidase4Feb 21, 2021
Deficiency of isobutyryl-CoA dehydrogenase7Mar 12, 2023
Deficiency of malonyl-CoA decarboxylase1Feb 19, 2023
Deficiency of phosphoserine phosphatase1Mar 5, 2021
Deficiency of steroid 11-beta-monooxygenase51Dec 7, 2023
Deficiency of steroid 17-alpha-monooxygenase61Dec 7, 2023
Deficiency of transaldolase7Mar 12, 2023
Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema6Mar 5, 2021
Dejerine-Sottas disease7Oct 2, 2023
Delayed speech and language development17Jul 17, 2021
Dent disease type 12Feb 19, 2023
Dent disease type 24Mar 5, 2021
Dentatorubral-pallidoluysian atrophy1Oct 2, 2023
Dentin dysplasia type I1Feb 21, 2021
Dermatitis, atopic, 23Mar 5, 2021
Desbuquois dysplasia 12Mar 5, 2021
Desbuquois dysplasia 21Mar 5, 2021
Desmin-related myofibrillar myopathy3Feb 19, 2023
Desmoid disease, hereditary4Feb 21, 2021
Desmosterolosis3Feb 21, 2021
Developmental and epileptic encephalopathy 1061Oct 2, 2023
Developmental and epileptic encephalopathy 1091Oct 2, 2023
Developmental and epileptic encephalopathy 9410Dec 14, 2023
Developmental and epileptic encephalopathy 981Mar 12, 2023
Developmental and epileptic encephalopathy, 12Feb 21, 2021
Developmental and epileptic encephalopathy, 1113Oct 2, 2023
Developmental and epileptic encephalopathy, 125Mar 5, 2021
Developmental and epileptic encephalopathy, 1317Oct 2, 2023
Developmental and epileptic encephalopathy, 148Oct 2, 2023
Developmental and epileptic encephalopathy, 153Mar 5, 2021
Developmental and epileptic encephalopathy, 161Mar 14, 2019
Developmental and epileptic encephalopathy, 172Mar 14, 2019
Developmental and epileptic encephalopathy, 1825Oct 2, 2023
Developmental and epileptic encephalopathy, 29Oct 2, 2023
Developmental and epileptic encephalopathy, 212Mar 5, 2021
Developmental and epileptic encephalopathy, 238Oct 2, 2023
Developmental and epileptic encephalopathy, 244Oct 2, 2023
Developmental and epileptic encephalopathy, 2510Oct 2, 2023
Developmental and epileptic encephalopathy, 269Oct 2, 2023
Developmental and epileptic encephalopathy, 277Oct 2, 2023
Developmental and epileptic encephalopathy, 2814Mar 12, 2023
Developmental and epileptic encephalopathy, 292Feb 19, 2023
Developmental and epileptic encephalopathy, 32Feb 19, 2023
Developmental and epileptic encephalopathy, 304Feb 21, 2021
Developmental and epileptic encephalopathy, 314Oct 2, 2023
Developmental and epileptic encephalopathy, 322Oct 2, 2023
Developmental and epileptic encephalopathy, 349Mar 5, 2021
Developmental and epileptic encephalopathy, 353Mar 5, 2021
Developmental and epileptic encephalopathy, 365Feb 19, 2023
Developmental and epileptic encephalopathy, 379Feb 19, 2023
Developmental and epileptic encephalopathy, 382Mar 5, 2021
Developmental and epileptic encephalopathy, 391Mar 5, 2021
Developmental and epileptic encephalopathy, 48Mar 5, 2021
Developmental and epileptic encephalopathy, 402Feb 21, 2021
Developmental and epileptic encephalopathy, 412Mar 5, 2021
Developmental and epileptic encephalopathy, 4217Mar 12, 2023
Developmental and epileptic encephalopathy, 435Oct 2, 2023
Developmental and epileptic encephalopathy, 442Feb 21, 2021
Developmental and epileptic encephalopathy, 451Mar 5, 2021
Developmental and epileptic encephalopathy, 467Mar 5, 2021
Developmental and epileptic encephalopathy, 472Oct 2, 2023
Developmental and epileptic encephalopathy, 487Mar 5, 2021
Developmental and epileptic encephalopathy, 495Feb 19, 2023
Developmental and epileptic encephalopathy, 59Oct 2, 2023
Developmental and epileptic encephalopathy, 5017Feb 19, 2023
Developmental and epileptic encephalopathy, 515Mar 5, 2021
Developmental and epileptic encephalopathy, 522Feb 21, 2021
Developmental and epileptic encephalopathy, 533Mar 5, 2021
Developmental and epileptic encephalopathy, 546Oct 2, 2023
Developmental and epileptic encephalopathy, 551Feb 21, 2021
Developmental and epileptic encephalopathy, 562Feb 21, 2021
Developmental and epileptic encephalopathy, 572Mar 5, 2021
Developmental and epileptic encephalopathy, 581Dec 14, 2023
Developmental and epileptic encephalopathy, 606Oct 2, 2023
Developmental and epileptic encephalopathy, 623Oct 2, 2023
Developmental and epileptic encephalopathy, 645Oct 2, 2023
Developmental and epileptic encephalopathy, 656Oct 2, 2023
Developmental and epileptic encephalopathy, 663Feb 19, 2023
Developmental and epileptic encephalopathy, 671Feb 19, 2023
Developmental and epileptic encephalopathy, 683Feb 19, 2023
Developmental and epileptic encephalopathy, 710Mar 12, 2023
Developmental and epileptic encephalopathy, 742Feb 21, 2021
Developmental and epileptic encephalopathy, 752Oct 2, 2023
Developmental and epileptic encephalopathy, 761Feb 19, 2023
Developmental and epileptic encephalopathy, 781Oct 2, 2023
Developmental and epileptic encephalopathy, 84Oct 2, 2023
Developmental and epileptic encephalopathy, 802Oct 2, 2023
Developmental and epileptic encephalopathy, 811Feb 19, 2023
Developmental and epileptic encephalopathy, 822Feb 19, 2023
Developmental and epileptic encephalopathy, 831Oct 2, 2023
Developmental and epileptic encephalopathy, 96Oct 2, 2023
Developmental and epileptic encephalopathy, 901Feb 19, 2023
Developmental delay and seizures with or without movement abnormalities3Oct 2, 2023
Developmental delay with autism spectrum disorder and gait instability38Dec 14, 2023
Developmental delay with dysmorphic facies and dental anomalies2Oct 2, 2023
Developmental delay with or without dysmorphic facies and autism9Oct 2, 2023
Developmental delay with short stature, dysmorphic facial features, and sparse hair4Mar 5, 2021
Developmental delay with short stature, dysmorphic facial features, and sparse hair 13Oct 2, 2023
Developmental delay with variable intellectual disability and dysmorphic facies1Dec 14, 2023
Developmental delay with variable intellectual impairment and behavioral abnormalities6Oct 2, 2023
Developmental delay, behavioral abnormalities, and neuropsychiatric disorders1Dec 14, 2023
Developmental delay, hypotonia, and impaired language1Oct 2, 2023
Developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy2Oct 2, 2023
Developmental delay, impaired speech, and behavioral abnormalities4Oct 2, 2023
Developmental delay, impaired speech, and behavioral abnormalities, with or without seizures1Oct 2, 2023
Developmental malformations-deafness-dystonia syndrome1Feb 10, 2021
Developmental regression2Feb 21, 2020
DiGeorge syndrome10Oct 2, 2023
Diabetes insipidus, nephrogenic, X-linked1Nov 14, 2016
Diabetes insipidus, nephrogenic, autosomal3Feb 21, 2021
Diabetes mellitus type 11Dec 7, 2023
Diabetes mellitus, transient neonatal, 34Mar 5, 2021
Diamond-Blackfan anemia 13Feb 19, 2023
Diamond-Blackfan anemia 102Feb 19, 2023
Diamond-Blackfan anemia 121Feb 21, 2021
Diamond-Blackfan anemia 36Feb 19, 2023
Diamond-Blackfan anemia 51Feb 10, 2021
Diamond-Blackfan anemia 65Dec 14, 2023
Diamond-Blackfan anemia 71Feb 19, 2023
Diamond-Blackfan anemia 83Mar 5, 2021
Diamond-Blackfan anemia 93Feb 10, 2021
Diaphragmatic hernia 31Feb 19, 2023
Diarrhea 11, malabsorptive, congenital1Oct 2, 2023
Dias-Logan syndrome2Feb 21, 2021
Diastrophic dysplasia2Feb 19, 2023
Dicarboxylic aminoaciduria1Mar 5, 2021
Diencephalic-mesencephalic junction dysplasia syndrome 15Feb 21, 2021
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome4Oct 2, 2023
Dihydropteridine reductase deficiency2Feb 21, 2021
Dihydropyrimidinase deficiency2Feb 21, 2021
Dihydropyrimidine dehydrogenase deficiency89Dec 7, 2023
Dilated cardiomyopathy 1A5Feb 19, 2023
Dilated cardiomyopathy 1AA3Feb 21, 2021
Dilated cardiomyopathy 1BB1Mar 5, 2021
Dilated cardiomyopathy 1C5Dec 14, 2023
Dilated cardiomyopathy 1CC6Mar 12, 2023
Dilated cardiomyopathy 1D2Oct 2, 2023
Dilated cardiomyopathy 1DD3Feb 19, 2023
Dilated cardiomyopathy 1EE5Oct 2, 2023
Dilated cardiomyopathy 1G72Oct 2, 2023
Dilated cardiomyopathy 1GG151Dec 7, 2023
Dilated cardiomyopathy 1HH1Mar 5, 2021
Dilated cardiomyopathy 1I2Feb 19, 2023
Dilated cardiomyopathy 1JJ2Mar 5, 2021
Dilated cardiomyopathy 1KK2Oct 2, 2023
Dilated cardiomyopathy 1L10Dec 7, 2023
Dilated cardiomyopathy 1O2Mar 5, 2021
Dilated cardiomyopathy 1P1Feb 21, 2021
Dilated cardiomyopathy 1R3Feb 19, 2023
Dilated cardiomyopathy 1S22Dec 14, 2023
Dilated cardiomyopathy 1W2Mar 5, 2021
Dilated cardiomyopathy 1X54Dec 7, 2023
Dilated cardiomyopathy 1Y4Feb 21, 2021
Dilated cardiomyopathy 1Z2Feb 19, 2023
Dilated cardiomyopathy 2A1Mar 5, 2021
Dilated cardiomyopathy 3B4Feb 19, 2023
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome2Oct 2, 2023
Dimethylglycine dehydrogenase deficiency1Feb 19, 2023
Distal 10q deletion syndrome1Apr 1, 2019
Distal 16p11.2 microdeletion syndrome2Apr 1, 2019
Distal arthrogryposis type 2B14Mar 5, 2021
Distal arthrogryposis type 5D2Feb 21, 2021
Distal myopathy with posterior leg and anterior hand involvement6Oct 2, 2023
Distichiasis-lymphedema syndrome3Mar 5, 2021
Dominant dystrophic epidermolysis bullosa with absence of skin2Mar 14, 2019
Donnai-Barrow syndrome12Feb 19, 2023
Drash syndrome53Dec 7, 2023
Dubin-Johnson syndrome5Feb 21, 2021
Duchenne muscular dystrophy16Feb 19, 2023
Dyggve-Melchior-Clausen syndrome1Mar 5, 2021
Dysarthria1Aug 17, 2015
Dyskeratosis congenita, X-linked3Dec 7, 2023
Dyskeratosis congenita, autosomal dominant 278Dec 7, 2023
Dyskeratosis congenita, autosomal dominant 31Dec 6, 2021
Dyskeratosis congenita, autosomal dominant 61Mar 5, 2021
Dyskeratosis congenita, autosomal recessive 21Feb 10, 2021
Dyskeratosis congenita, autosomal recessive 32Dec 7, 2023
Dyskeratosis congenita, autosomal recessive 578Dec 7, 2023
Dyskeratosis congenita, autosomal recessive 62Mar 5, 2021
Dyskinesia with orofacial involvement, autosomal dominant6Dec 14, 2023
Dyslexia, susceptibility to, 21Mar 5, 2021
Dysmorphic features4Jan 10, 2017
Dyssynergia2Nov 12, 2016
Dystonia 129Oct 2, 2023
Dystonia 162Mar 14, 2019
Dystonia 232Mar 5, 2021
Dystonia 272Feb 19, 2023
Dystonia 28, childhood-onset8Mar 5, 2021
Dystonia 331Oct 2, 2023
Dystonia 52Feb 19, 2023
Dystonia 94Mar 5, 2021
Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities1Feb 21, 2021
Dystonic disorder1Aug 17, 2015
EAST syndrome3Feb 19, 2023
EEM syndrome2Feb 19, 2023
EIF3G-related autism spectrum disorder1Dec 14, 2023
Early-onset Lafora body disease2Mar 5, 2021
Early-onset generalized limb-onset dystonia3Mar 5, 2021
Early-onset myopathy with fatal cardiomyopathy51Dec 14, 2023
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome24Oct 2, 2023
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome4Mar 5, 2021
Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive1Feb 19, 2023
Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive2Mar 5, 2021
Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis2Feb 21, 2021
Ectodermal dysplasia and immunodeficiency 21Mar 5, 2021
Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies1Feb 19, 2023
Ectodermal dysplasia-syndactyly syndrome 12Mar 5, 2021
Ectopia lentis 1, isolated, autosomal dominant1Feb 21, 2021
Ectopia lentis et pupillae1Feb 19, 2023
Ehlers-Danlos syndrome due to tenascin-X deficiency10Oct 2, 2023
Ehlers-Danlos syndrome progeroid type2Mar 5, 2021
Ehlers-Danlos syndrome, cardiac valvular type1Mar 14, 2019
Ehlers-Danlos syndrome, classic type3Apr 1, 2019
Ehlers-Danlos syndrome, classic type, 19Oct 2, 2023
Ehlers-Danlos syndrome, classic type, 23Feb 19, 2023
Ehlers-Danlos syndrome, classic-like, 23Mar 5, 2021
Ehlers-Danlos syndrome, dermatosparaxis type7Mar 5, 2021
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type2Feb 21, 2021
Ehlers-Danlos syndrome, kyphoscoliotic type 19Oct 2, 2023
Ehlers-Danlos syndrome, musculocontractural type 12Mar 5, 2021
Ehlers-Danlos syndrome, musculocontractural type 26Feb 21, 2021
Ehlers-Danlos syndrome, periodontal type 21Oct 2, 2023
Ehlers-Danlos syndrome, spondylodysplastic type, 12Feb 19, 2023
Ehlers-Danlos syndrome, spondylodysplastic type, 23Mar 5, 2021
Ehlers-Danlos syndrome, type 411Dec 14, 2023
Ehlers-danlos syndrome, arthrochalasia type, 22Mar 5, 2021
Eichsfeld type congenital muscular dystrophy1Feb 21, 2021
Elliptocytosis 25Mar 5, 2021
Elliptocytosis 37Mar 5, 2021
Ellis-van Creveld syndrome10Mar 5, 2021
Emery-Dreifuss muscular dystrophy 1, X-linked2Dec 7, 2023
Emery-Dreifuss muscular dystrophy 3, autosomal recessive1Dec 14, 2023
Emery-Dreifuss muscular dystrophy 4, autosomal dominant29Oct 2, 2023
Emery-Dreifuss muscular dystrophy 5, autosomal dominant11Feb 19, 2023
Encephalitis/encephalopathy, mild, with reversible myelin vacuolization5Oct 2, 2023
Encephalocraniocutaneous lipomatosis3Feb 21, 2021
Encephalopathy due to GLUT1 deficiency5Oct 2, 2023
Encephalopathy due to defective mitochondrial and peroxisomal fission 23Mar 5, 2021
Encephalopathy, acute, infection-induced, susceptibility to, 465Dec 7, 2023
Encephalopathy, acute, infection-induced, susceptibility to, 93Feb 19, 2023
Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 18Oct 2, 2023
Encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities3Mar 5, 2021
Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 12Feb 21, 2021
Encephalopathy, progressive, early-onset, with episodic rhabdomyolysis3Feb 19, 2023
Encephalopathy, progressive, with amyotrophy and optic atrophy4Mar 5, 2021
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome2Mar 5, 2021
Endometrial carcinoma933Dec 7, 2023
Enhanced S-cone syndrome62Dec 7, 2023
Enterokinase deficiency3Mar 5, 2021
Epidermolysis bullosa pruriginosa2Mar 14, 2019
Epidermolysis bullosa simplex1Oct 16, 2017
Epidermolysis bullosa simplex 1C, localized1Feb 21, 2021
Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency6Oct 2, 2023
Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive1Feb 21, 2021
Epidermolysis bullosa simplex 5B, with muscular dystrophy1Mar 5, 2021
Epidermolysis bullosa simplex 5C, with pyloric atresia4Mar 5, 2021
Epidermolysis bullosa simplex 7, with nephropathy and deafness2Feb 21, 2021
Epidermolysis bullosa simplex with nail dystrophy4Feb 21, 2021
Epidermolysis bullosa simplex, Ogna type2Feb 19, 2023
Epidermolysis bullosa, junctional 2A, intermediate1Feb 19, 2023
Epidermolysis bullosa, junctional 2B, severe1Feb 19, 2023
Epidermolysis bullosa, junctional 5A, intermediate3Oct 2, 2023
Epilepsy4Jan 10, 2017
Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders4Feb 19, 2023
Epilepsy, childhood absence 21Mar 14, 2019
Epilepsy, childhood absence, susceptibility to, 51Aug 17, 2015
Epilepsy, childhood absence, susceptibility to, 617Mar 5, 2021
Epilepsy, early-onset, 3, with or without developmental delay1Dec 14, 2023
Epilepsy, early-onset, vitamin B6-dependent5Mar 5, 2021
Epilepsy, familial adult myoclonic, 23Mar 5, 2021
Epilepsy, familial adult myoclonic, 53Mar 5, 2021
Epilepsy, familial focal, with variable foci 115Dec 14, 2023
Epilepsy, familial focal, with variable foci 22Feb 19, 2023
Epilepsy, familial focal, with variable foci 32Oct 2, 2023
Epilepsy, familial focal, with variable foci 47Oct 2, 2023
Epilepsy, familial temporal lobe, 13Feb 21, 2021
Epilepsy, idiopathic generalized, susceptibility to, 102Mar 5, 2021
Epilepsy, idiopathic generalized, susceptibility to, 112Dec 14, 2023
Epilepsy, idiopathic generalized, susceptibility to, 121Mar 14, 2019
Epilepsy, idiopathic generalized, susceptibility to, 142Oct 2, 2023
Epilepsy, idiopathic generalized, susceptibility to, 151Oct 2, 2023
Epilepsy, idiopathic generalized, susceptibility to, 71Oct 16, 2017
Epilepsy, idiopathic generalized, susceptibility to, 92Feb 19, 2023
Epilepsy, progressive myoclonic, 1B1Oct 2, 2023
Epileptic encephalopathy5Nov 14, 2016
Epileptic encephalopathy, infantile or early childhood, 12Apr 16, 2021
Epileptic encephalopathy, infantile or early childhood, 22Feb 21, 2021
Epileptic encephalopathy, infantile or early childhood, 31Feb 21, 2021
Epiphyseal dysplasia, multiple, 31Nov 14, 2016
Epiphyseal dysplasia, multiple, 61Nov 14, 2016
Episodic ataxia type 11Feb 21, 2021
Episodic ataxia type 219Dec 14, 2023
Episodic ataxia type 51Feb 19, 2023
Episodic ataxia type 62Feb 19, 2023
Episodic flaccid weakness4Sep 3, 2015
Episodic kinesigenic dyskinesia 12Mar 5, 2021
Episodic pain syndrome, familial, 23Feb 19, 2023
Epsilon-trimethyllysine hydroxylase deficiency1Oct 16, 2017
Erythrocytosis, familial, 71Sep 21, 2023
Essential hypertension1Mar 5, 2021
Ethylmalonic encephalopathy30Dec 7, 2023
Euthyroid goiter8Feb 11, 2022
Exostoses, multiple, type 272Dec 7, 2023
Expressive language delay12Jul 10, 2017
Exudative vitreoretinopathy 11Mar 5, 2021
Exudative vitreoretinopathy 41Feb 21, 2021
Exudative vitreoretinopathy 51Feb 21, 2021
Exudative vitreoretinopathy 72Mar 5, 2021
FG syndrome 13Feb 19, 2023
FG syndrome 23Feb 21, 2021
FG syndrome 42Feb 21, 2021
FLNA related disorders1Oct 16, 2017
FRAXE7Feb 19, 2023
Fabry disease2Feb 21, 2021
Facial dysmorphism-immunodeficiency-livedo-short stature syndrome14Feb 11, 2022
Facioscapulohumeral muscular dystrophy 21Oct 2, 2023
Factor H deficiency5Oct 2, 2023
Factor I deficiency1Feb 19, 2023
Factor V deficiency2Mar 5, 2021
Factor VII deficiency2Feb 21, 2021
Factor XII deficiency disease2Dec 14, 2023
Factor XIII, b subunit, deficiency of1Mar 5, 2021
Failure to thrive7Jan 10, 2017
Familial Mediterranean fever2Feb 19, 2023
Familial Mediterranean fever, autosomal dominant19Dec 7, 2023
Familial X-linked hypophosphatemic vitamin D refractory rickets3Feb 21, 2021
Familial acute necrotizing encephalopathy3Feb 21, 2021
Familial adenomatous polyposis 1648Dec 7, 2023
Familial adenomatous polyposis 2220Dec 7, 2023
Familial adenomatous polyposis 3123Dec 7, 2023
Familial adenomatous polyposis 43Mar 5, 2021
Familial amyloid nephropathy with urticaria AND deafness1Feb 21, 2021
Familial amyloid neuropathy1Feb 19, 2023
Familial cancer of breast3608Dec 7, 2023
Familial chronic mucocutaneous candidiasis1Feb 21, 2021
Familial cold autoinflammatory syndrome 11Feb 21, 2021
Familial cold autoinflammatory syndrome 26Oct 2, 2023
Familial cold autoinflammatory syndrome 42Mar 5, 2021
Familial dysautonomia4Feb 11, 2022
Familial dysfibrinogenemia1Oct 2, 2023
Familial episodic pain syndrome with predominantly lower limb involvement1Mar 5, 2021
Familial episodic pain syndrome with predominantly upper body involvement1Mar 5, 2021
Familial expansile osteolysis3Mar 5, 2021
Familial gestational hyperthyroidism2Dec 7, 2023
Familial hemophagocytic lymphohistiocytosis 25Feb 21, 2021
Familial hemophagocytic lymphohistiocytosis 39Mar 5, 2021
Familial hemophagocytic lymphohistiocytosis 412Dec 7, 2023
Familial hemophagocytic lymphohistiocytosis 540Dec 7, 2023
Familial hyperaldosteronism type II1Feb 21, 2021
Familial hyperaldosteronism type III3Feb 19, 2023
Familial hypobetalipoproteinemia 17Oct 2, 2023
Familial hypocalciuric hypercalcemia 11Feb 19, 2023
Familial hypocalciuric hypercalcemia 31Feb 21, 2021
Familial hypokalemia-hypomagnesemia10Oct 2, 2023
Familial infantile myasthenia40Dec 7, 2023
Familial infantile myoclonic epilepsy1Mar 14, 2019
Familial isolated deficiency of vitamin E31Dec 7, 2023
Familial medullary thyroid carcinoma12Dec 6, 2021
Familial meningioma114Dec 7, 2023
Familial partial lipodystrophy, Dunnigan type1Oct 2, 2023
Familial renal glucosuria1Oct 2, 2023
Familial spontaneous pneumothorax3Mar 5, 2021
Familial steroid-resistant nephrotic syndrome with sensorineural deafness1Oct 2, 2023
Familial temporal lobe epilepsy 54Mar 5, 2021
Familial temporal lobe epilepsy 73Feb 19, 2023
Familial thyroid dyshormonogenesis 11Mar 5, 2021
Familial type 5 hyperlipoproteinemia1Feb 19, 2023
Fanconi anemia complementation group A265Dec 7, 2023
Fanconi anemia complementation group B4Dec 7, 2023
Fanconi anemia complementation group C83Dec 7, 2023
Fanconi anemia complementation group D13Mar 5, 2021
Fanconi anemia complementation group D295Dec 7, 2023
Fanconi anemia complementation group E49Dec 7, 2023
Fanconi anemia complementation group F28Dec 7, 2023
Fanconi anemia complementation group G76Dec 7, 2023
Fanconi anemia complementation group I114Dec 7, 2023
Fanconi anemia complementation group J4Dec 6, 2021
Fanconi anemia complementation group L43Dec 7, 2023
Fanconi anemia complementation group N6Feb 11, 2022
Fanconi anemia complementation group O6Mar 12, 2023
Fanconi anemia complementation group P43Dec 7, 2023
Fanconi anemia complementation group Q23Dec 7, 2023
Fanconi anemia complementation group U2Feb 21, 2021
Fanconi anemia, complementation group S2Feb 10, 2021
Fanconi anemia, complementation group W1Feb 19, 2023
Fanconi renotubular syndrome 11Oct 2, 2023
Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young2Dec 14, 2023
Farber lipogranulomatosis3Mar 5, 2021
Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 335Dec 7, 2023
Febrile seizures, familial, 43Mar 5, 2021
Febrile seizures, familial, 82Oct 2, 2023
Ferguson-Bonni neurodevelopmental syndrome1Feb 19, 2023
Fetal akinesia deformation sequence 117Feb 19, 2023
Fetal akinesia deformation sequence 246Dec 7, 2023
Fetal akinesia deformation sequence 351Dec 7, 2023
Fetal akinesia deformation sequence 42Feb 19, 2023
Fetal hemoglobin quantitative trait locus 11Feb 21, 2021
Fibrochondrogenesis 15Mar 5, 2021
Fibromatosis, gingival, 12Dec 7, 2023
Fibromatosis, gingival, 51Feb 10, 2021
Fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement1Feb 21, 2021
Fibrosis, neurodegeneration, and cerebral angiomatosis1Feb 21, 2021
Filippi syndrome3Mar 5, 2021
Finnish congenital nephrotic syndrome150Dec 7, 2023
Floating-Harbor syndrome11Feb 19, 2023
Focal dermal hypoplasia3Dec 14, 2023
Focal segmental glomerulosclerosis 12Mar 5, 2021
Focal segmental glomerulosclerosis 24Mar 5, 2021
Focal segmental glomerulosclerosis 3, susceptibility to2Feb 21, 2021
Focal segmental glomerulosclerosis 4, susceptibility to1Mar 5, 2021
Focal segmental glomerulosclerosis 51Feb 19, 2023
Focal segmental glomerulosclerosis 63Oct 2, 2023
Focal segmental glomerulosclerosis 82Feb 19, 2023
Focal segmental glomerulosclerosis 95Mar 5, 2021
Focal segmental glomerulosclerosis and neurodevelopmental syndrome1Dec 14, 2023
Fontaine progeroid syndrome2Oct 2, 2023
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome1Mar 5, 2021
Fowler syndrome1Mar 5, 2021
Fragile X syndrome2Feb 21, 2021
Frank-Ter Haar syndrome1Feb 21, 2021
Fraser syndrome 17Oct 2, 2023
Fraser syndrome 21Mar 5, 2021
Fraser syndrome 31Mar 12, 2023
Frasier syndrome2Feb 21, 2021
Freeman-Sheldon syndrome2Feb 19, 2023
Friedreich ataxia 11Mar 5, 2021
Frontometaphyseal dysplasia 21Mar 5, 2021
Frontonasal dysplasia with alopecia and genital anomaly1Mar 5, 2021
Frontotemporal dementia and/or amyotrophic lateral sclerosis 31Feb 19, 2023
Frontotemporal dementia and/or amyotrophic lateral sclerosis 42Feb 21, 2021
Frontotemporal dementia and/or amyotrophic lateral sclerosis 51Oct 2, 2023
Frontotemporal dementia and/or amyotrophic lateral sclerosis 62Mar 5, 2021
Frontotemporal dementia and/or amyotrophic lateral sclerosis 849Dec 7, 2023
Fructose-biphosphatase deficiency1Feb 19, 2023
Fumarase deficiency90Dec 7, 2023
GAPO syndrome1Mar 5, 2021
GAPVD1-related Nephrotic syndrome1Oct 2, 2023
GEN1-related prostate cancer1Dec 7, 2023
GJB2-Related Autosomal Recessive Nonsyndromic Hearing Loss1Dec 14, 2023
GM1 gangliosidosis type 23Mar 14, 2019
GM1 gangliosidosis type 33Feb 21, 2021
GM3 synthase deficiency7Feb 21, 2021
GNE myopathy52Dec 7, 2023
GRACILE syndrome3Mar 12, 2023
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions2Feb 21, 2021
Gabriele de Vries syndrome5Feb 19, 2023
Galactosylceramide beta-galactosidase deficiency16Oct 2, 2023
Galloway-Mowat syndrome 15Feb 19, 2023
Galloway-Mowat syndrome 33Mar 5, 2021
Galloway-Mowat syndrome 43Mar 5, 2021
Gamma-aminobutyric acid transaminase deficiency11Dec 7, 2023
Gastric cancer1Mar 5, 2021
Gastrointestinal stromal tumor200Dec 7, 2023
Gaucher disease perinatal lethal2Feb 21, 2021
Gaucher disease type I35Dec 14, 2023
Gaucher disease type II31Feb 21, 2021
Gaucher disease type III30Sep 27, 2019
Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome30Sep 27, 2019
Gaze palsy, familial horizontal, with progressive scoliosis 11Oct 16, 2017
Gaze palsy, familial horizontal, with progressive scoliosis, 21Mar 5, 2021
Generalized dominant dystrophic epidermolysis bullosa3Mar 14, 2019
Generalized epilepsy with febrile seizures plus, type 12Feb 19, 2023
Generalized epilepsy with febrile seizures plus, type 101Oct 2, 2023
Generalized epilepsy with febrile seizures plus, type 211Oct 2, 2023
Generalized epilepsy with febrile seizures plus, type 712Mar 5, 2021
Generalized epilepsy with febrile seizures plus, type 93Oct 2, 2023
Generalized epilepsy-paroxysmal dyskinesia syndrome1Oct 16, 2017
Generalized juvenile polyposis/juvenile polyposis coli1Mar 5, 2021
Generalized pustular psoriasis1Feb 21, 2021
Genitopatellar syndrome9Mar 5, 2021
Genitourinary and/or brain malformation syndrome1Feb 19, 2023
Geroderma osteodysplastica1Mar 5, 2021
Ghosal hematodiaphyseal dysplasia1Feb 21, 2021
Giant axonal neuropathy 14Feb 21, 2021
Giant axonal neuropathy 21Feb 19, 2023
Gillespie syndrome11Oct 2, 2023
Gillessen-Kaesbach-Nishimura syndrome1Feb 19, 2023
Glanzmann thrombasthenia2Mar 5, 2021
Glanzmann thrombasthenia 11Feb 19, 2023
Glaucoma 1, open angle, A1Feb 19, 2023
Glaucoma 3, primary congenital, D2Feb 11, 2022
Glaucoma 3, primary congenital, E1Oct 2, 2023
Glaucoma 3A5Mar 12, 2023
Glioma susceptibility 248Dec 7, 2023
Global developmental delay37Jul 17, 2021
Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome187Dec 7, 2023
Global developmental delay with or without impaired intellectual development5Feb 19, 2023
Global developmental delay with speech and behavioral abnormalities3Dec 14, 2023
Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies2Mar 5, 2021
Glomerulopathy with fibronectin deposits 21Mar 5, 2021
Glomuvenous malformation1Feb 19, 2023
Glucocorticoid deficiency 12Feb 19, 2023
Glucocorticoid deficiency 44Feb 21, 2021
Glucocorticoid deficiency with achalasia1Feb 21, 2021
Glucocorticoid resistance2Feb 19, 2023
Glucose-6-phosphate transport defect68Dec 7, 2023
Glutamate formiminotransferase deficiency2Mar 12, 2023
Glutamate pyruvate transaminase 2 deficiency3Mar 5, 2021
Glutaric aciduria, type 1121Dec 7, 2023
Glycogen storage disease IXa16Dec 14, 2023
Glycogen storage disease IXb2Feb 19, 2023
Glycogen storage disease IXc6Dec 14, 2023
Glycogen storage disease IXd6Oct 2, 2023
Glycogen storage disease XV1Feb 19, 2023
Glycogen storage disease due to glucose-6-phosphatase deficiency type IA20Feb 19, 2023
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency1Feb 21, 2021
Glycogen storage disease due to muscle and heart glycogen synthase deficiency5Oct 2, 2023
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency1Oct 2, 2023
Glycogen storage disease type III150Dec 7, 2023
Glycogen storage disease type X3Oct 2, 2023
Glycogen storage disease, type II241Dec 7, 2023
Glycogen storage disease, type IV85Dec 14, 2023
Glycogen storage disease, type V107Dec 14, 2023
Glycogen storage disease, type VI8Feb 19, 2023
Glycogen storage disease, type VII42Dec 14, 2023
Glycogen storage disorder due to hepatic glycogen synthase deficiency2Feb 19, 2023
Glycosylphosphatidylinositol biosynthesis defect 155Mar 5, 2021
Glycosylphosphatidylinositol biosynthesis defect 164Mar 5, 2021
Glycosylphosphatidylinositol biosynthesis defect 183Feb 21, 2021
Glycosylphosphatidylinositol biosynthesis defect 211Feb 19, 2023
Gnathodiaphyseal dysplasia2Mar 5, 2021
Gnb5-related intellectual disability-cardiac arrhythmia syndrome2Mar 5, 2021
Gordon syndrome4Mar 5, 2021
Gorlin syndrome18Dec 6, 2021
Grange syndrome3Feb 19, 2023
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative2Mar 5, 2021
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 22Mar 5, 2021
Gray platelet syndrome4Feb 21, 2021
Grebe syndrome1Feb 21, 2021
Griscelli syndrome type 12Mar 5, 2021
Griscelli syndrome type 21Mar 14, 2019
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome3Mar 5, 2021
Growth delay due to insulin-like growth factor I resistance11Oct 2, 2023
Growth delay due to insulin-like growth factor type 1 deficiency1Mar 5, 2021
Growth hormone insensitivity with immune dysregulation 1, autosomal recessive1Feb 21, 2021
Growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy12Mar 5, 2021
H syndrome2Feb 19, 2023
HSD10 mitochondrial disease2Feb 21, 2021
Hajdu-Cheney syndrome5Oct 2, 2023
Hao-Fountain syndrome1Feb 19, 2023
Harel-Yoon syndrome8Feb 19, 2023
Hartsfield-Bixler-Demyer syndrome4Feb 19, 2023
Hb SS disease41Feb 19, 2023
Hearing loss, autosomal dominant 371Feb 19, 2023
Hearing loss, autosomal dominant 712Feb 19, 2023
Hearing loss, autosomal dominant 721Feb 21, 2021
Hearing loss, autosomal dominant 754Oct 2, 2023
Hearing loss, autosomal dominant 833Feb 19, 2023
Hearing loss, autosomal dominant 841Oct 2, 2023
Hearing loss, autosomal recessive 1062Feb 21, 2021
Hearing loss, autosomal recessive 1071Feb 21, 2021
Hearing loss, autosomal recessive 1081Feb 21, 2021
Hearing loss, autosomal recessive 1111Mar 5, 2021
Hearing loss, autosomal recessive 1121Feb 21, 2021
Hearing loss, autosomal recessive 575Oct 2, 2023
Hearing loss, autosomal recessive 941Feb 21, 2021
Hearing loss, autosomal recessive 992Feb 21, 2021
Heart and brain malformation syndrome1Feb 21, 2021
Heart defect - tongue hamartoma - polysyndactyly syndrome1Oct 16, 2017
Heart, malformation of1Oct 16, 2017
Heimler syndrome 1140Dec 7, 2023
Heimler syndrome 2103Dec 7, 2023
Heinz body anemia1Sep 21, 2023
Hemochromatosis type 13Dec 14, 2023
Hemochromatosis type 357Dec 7, 2023
Hemoglobin H disease1Sep 21, 2023
Hemolytic anemia due to glucophosphate isomerase deficiency3Mar 5, 2021
Hemolytic anemia due to hexokinase deficiency3Mar 5, 2021
Hemolytic uremic syndrome, atypical, susceptibility to, 13Mar 5, 2021
Hemorrhage, intracerebral, susceptibility to1Mar 5, 2021
Hennekam lymphangiectasia-lymphedema syndrome 13Feb 21, 2021
Hennekam lymphangiectasia-lymphedema syndrome 213Feb 19, 2023
Hepatic veno-occlusive disease-immunodeficiency syndrome5Oct 2, 2023
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 187Dec 7, 2023
Hereditary acrodermatitis enteropathica1Feb 21, 2021
Hereditary angioedema type 13Mar 5, 2021
Hereditary antithrombin deficiency1Feb 21, 2021
Hereditary breast cancer, ABRAXAS1-related1Dec 7, 2023
Hereditary coproporphyria1Mar 12, 2023
Hereditary cryohydrocytosis with reduced stomatin1Mar 14, 2019
Hereditary diffuse gastric adenocarcinoma1Feb 19, 2023
Hereditary diffuse leukoencephalopathy with spheroids5Mar 5, 2021
Hereditary factor VIII deficiency disease4Feb 19, 2023
Hereditary factor XI deficiency disease1Mar 5, 2021
Hereditary fructosuria35Dec 7, 2023
Hereditary hypotrichosis with recurrent skin vesicles1Feb 19, 2023
Hereditary insensitivity to pain with anhidrosis7Mar 5, 2021
Hereditary intrinsic factor deficiency1Mar 5, 2021
Hereditary liability to pressure palsies6Feb 21, 2021
Hereditary lymphedema type I2Feb 19, 2023
Hereditary motor and sensory neuropathy with optic atrophy1Mar 5, 2021
Hereditary mucoepithelial dysplasia1Oct 2, 2023
Hereditary nonpolyposis colon cancer5Dec 7, 2023
Hereditary pancreatitis6Dec 7, 2023
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement2Mar 5, 2021
Hereditary sensory and autonomic neuropathy type 11Aug 17, 2015
Hereditary sensory and autonomic neuropathy type 68Feb 19, 2023
Hereditary sensory and autonomic neuropathy type 71Oct 2, 2023
Hereditary sensory and autonomic neuropathy with spastic paraplegia2Mar 5, 2021
Hereditary spastic paraplegia 101Feb 21, 2021
Hereditary spastic paraplegia 116Feb 19, 2023
Hereditary spastic paraplegia 123Feb 19, 2023
Hereditary spastic paraplegia 1514Mar 5, 2021
Hereditary spastic paraplegia 171Feb 21, 2021
Hereditary spastic paraplegia 181Feb 19, 2023
Hereditary spastic paraplegia 24Feb 21, 2021
Hereditary spastic paraplegia 232Feb 19, 2023
Hereditary spastic paraplegia 265Dec 14, 2023
Hereditary spastic paraplegia 3013Dec 14, 2023
Hereditary spastic paraplegia 311Mar 5, 2021
Hereditary spastic paraplegia 353Mar 5, 2021
Hereditary spastic paraplegia 3A3Mar 14, 2019
Hereditary spastic paraplegia 45Dec 14, 2023
Hereditary spastic paraplegia 421Feb 21, 2021
Hereditary spastic paraplegia 431Feb 21, 2021
Hereditary spastic paraplegia 441Mar 5, 2021
Hereditary spastic paraplegia 451Feb 21, 2021
Hereditary spastic paraplegia 466Mar 5, 2021
Hereditary spastic paraplegia 476Mar 5, 2021
Hereditary spastic paraplegia 4814Oct 2, 2023
Hereditary spastic paraplegia 4910Mar 5, 2021
Hereditary spastic paraplegia 506Feb 19, 2023
Hereditary spastic paraplegia 513Oct 2, 2023
Hereditary spastic paraplegia 532Feb 19, 2023
Hereditary spastic paraplegia 543Oct 2, 2023
Hereditary spastic paraplegia 551Oct 16, 2017
Hereditary spastic paraplegia 563Mar 5, 2021
Hereditary spastic paraplegia 572Mar 5, 2021
Hereditary spastic paraplegia 5A1Oct 16, 2017
Hereditary spastic paraplegia 634Mar 5, 2021
Hereditary spastic paraplegia 641Feb 21, 2021
Hereditary spastic paraplegia 77Mar 12, 2023
Hereditary spastic paraplegia 722Feb 21, 2021
Hereditary spastic paraplegia 742Feb 19, 2023
Hereditary spastic paraplegia 752Feb 21, 2021
Hereditary spastic paraplegia 773Mar 12, 2023
Hereditary spastic paraplegia 82Feb 21, 2021
Hereditary spherocytosis type 14Oct 2, 2023
Hereditary spherocytosis type 22Oct 2, 2023
Hereditary spherocytosis type 33Mar 5, 2021
Hereditary spherocytosis type 41Feb 21, 2021
Hereditary xanthinuria type 11Feb 21, 2021
Hermansky-Pudlak syndrome 167Dec 7, 2023
Hermansky-Pudlak syndrome 219Dec 7, 2023
Hermansky-Pudlak syndrome 388Dec 7, 2023
Hermansky-Pudlak syndrome 432Dec 7, 2023
Hermansky-Pudlak syndrome 61Feb 21, 2021
Hermansky-Pudlak syndrome 71Mar 5, 2021
Hermansky-Pudlak syndrome 81Mar 5, 2021
Hermansky-Pudlak syndrome 91Mar 5, 2021
Heterotaxy, visceral, 1, X-linked1Mar 5, 2021
Heterotaxy, visceral, 10, autosomal, with male infertility1Feb 19, 2023
Heterotaxy, visceral, 12, autosomal2Oct 2, 2023
Heterotaxy, visceral, 4, autosomal2Feb 19, 2023
Heterotaxy, visceral, 5, autosomal3Feb 19, 2023
Heterotaxy, visceral, 6, autosomal3Feb 19, 2023
Heterotaxy, visceral, 7, autosomal2Feb 21, 2021
Heterotaxy, visceral, 8, autosomal10Oct 2, 2023
Heterotaxy, visceral, 9, autosomal, with male infertility1Oct 2, 2023
Heterotopia, periventricular, X-linked dominant4Oct 2, 2023
Hiatt-Neu-Cooper neurodevelopmental syndrome1Oct 2, 2023
High myopia-sensorineural deafness syndrome1Mar 5, 2021
Hirschsprung disease, susceptibility to, 1131Dec 7, 2023
Histiocytic medullary reticulosis46Dec 7, 2023
Hogue-Janssens syndrome 16Oct 2, 2023
Holocarboxylase synthetase deficiency57Dec 7, 2023
Holoprosencephaly 12 with or without pancreatic agenesis1Feb 19, 2023
Holoprosencephaly 13, X-linked1Oct 2, 2023
Holoprosencephaly 31Nov 14, 2016
Holoprosencephaly 42Dec 14, 2023
Holoprosencephaly 52Feb 19, 2023
Holoprosencephaly 71Feb 10, 2021
Holoprosencephaly 94Feb 19, 2023
Holt-Oram syndrome7Oct 2, 2023
Homocystinuria due to methylene tetrahydrofolate reductase deficiency3Mar 5, 2021
Houge-Janssens syndrome 25Oct 2, 2023
Houge-Janssens syndrome 33Feb 19, 2023
Hurler syndrome4Mar 5, 2021
Hurthle cell carcinoma of thyroid2Dec 14, 2023
Hutchinson-Gilford syndrome1Feb 21, 2021
Hyaline fibromatosis syndrome5Mar 5, 2021
Hydatidiform mole, recurrent, 11Feb 21, 2021
Hydrocephalus, congenital, 3, with brain anomalies4Feb 19, 2023
Hydrocephalus, nonsyndromic, autosomal recessive 14Mar 5, 2021
Hydrocephalus, nonsyndromic, autosomal recessive 218Oct 2, 2023
Hydrolethalus syndrome 23Feb 19, 2023
Hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome4Feb 19, 2023
Hyper-IgE recurrent infection syndrome 1, autosomal dominant2Oct 2, 2023
Hyper-IgE recurrent infection syndrome 3, autosomal recessive2Feb 21, 2021
Hyper-IgE recurrent infection syndrome 4, autosomal recessive1Feb 21, 2021
Hyper-IgM syndrome type 31Feb 21, 2021
Hyper-IgM syndrome type 53Mar 5, 2021
Hyperaldosteronism, familial, type IV1Feb 21, 2021
Hyperammonemia, type III36Dec 7, 2023
Hyperbiliverdinemia1Feb 21, 2021
Hypercalcemia, infantile, 13Mar 5, 2021
Hypercalcemia, infantile, 21Feb 21, 2021
Hypercholanemia, familial 12Feb 21, 2021
Hypercholesterolemia, autosomal dominant, 33Oct 2, 2023
Hypercholesterolemia, autosomal dominant, type B5Oct 2, 2023
Hypercholesterolemia, familial, 13Feb 19, 2023
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency1Oct 2, 2023
Hyperekplexia 11Feb 21, 2021
Hyperekplexia 38Feb 19, 2023
Hyperimmunoglobulin D with periodic fever4Feb 21, 2021
Hyperinsulinemic hypoglycemia, familial, 12Mar 5, 2021
Hyperinsulinism due to INSR deficiency1Feb 21, 2021
Hyperinsulinism due to glucokinase deficiency4Feb 19, 2023
Hyperinsulinism-hyperammonemia syndrome2Feb 21, 2021
Hyperkalemic periodic paralysis3Feb 21, 2021
Hyperlipidemia, familial combined, LPL related1Feb 21, 2021
Hyperlipoproteinemia, type 1D1Mar 12, 2023
Hyperlipoproteinemia, type I5Oct 2, 2023
Hyperlysinemia1Feb 21, 2021
Hypermanganesemia with dystonia, polycythemia, and cirrhosis1Feb 19, 2023
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome32Dec 7, 2023
Hyperparathyroidism 126Dec 7, 2023
Hyperparathyroidism, transient neonatal2Feb 21, 2021
Hyperphenylalaninemia due to DNAJC12 deficiency1Feb 19, 2023
Hyperphosphatasemia with bone disease1Oct 2, 2023
Hyperphosphatasia with intellectual disability syndrome 16Mar 5, 2021
Hyperphosphatasia with intellectual disability syndrome 26Feb 19, 2023
Hyperphosphatasia with intellectual disability syndrome 31Feb 21, 2021
Hyperphosphatasia with intellectual disability syndrome 44Mar 5, 2021
Hyperphosphatasia with intellectual disability syndrome 54Feb 19, 2023
Hyperphosphatasia with intellectual disability syndrome 63Mar 5, 2021
Hyperprolinemia type 23Mar 5, 2021
Hypertrichotic osteochondrodysplasia Cantu type2Mar 14, 2019
Hypertriglyceridemia 11Feb 19, 2023
Hypertrophic cardiomyopathy 116Dec 14, 2023
Hypertrophic cardiomyopathy 112Feb 19, 2023
Hypertrophic cardiomyopathy 121Feb 21, 2021
Hypertrophic cardiomyopathy 131Feb 19, 2023
Hypertrophic cardiomyopathy 143Feb 19, 2023
Hypertrophic cardiomyopathy 174Feb 19, 2023
Hypertrophic cardiomyopathy 181Feb 21, 2021
Hypertrophic cardiomyopathy 203Feb 19, 2023
Hypertrophic cardiomyopathy 251Feb 21, 2021
Hypertrophic cardiomyopathy 268Oct 2, 2023
Hypertrophic cardiomyopathy 33Oct 2, 2023
Hypertrophic cardiomyopathy 419Dec 14, 2023
Hypertrophic cardiomyopathy 61Feb 10, 2021
Hypertrophic cardiomyopathy 73Mar 5, 2021
Hypertrophic cardiomyopathy 81Feb 19, 2023
Hypertrophic cardiomyopathy 930Oct 2, 2023
Hypertrophic osteoarthropathy, primary, autosomal recessive, 21Mar 5, 2021
Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome3Feb 19, 2023
Hypoalphalipoproteinemia, primary, 16Oct 2, 2023
Hypochondroplasia1Mar 14, 2019
Hypogonadotropic hypogonadism 1 with or without anosmia2Feb 21, 2021
Hypogonadotropic hypogonadism 16 with or without anosmia1Apr 1, 2019
Hypogonadotropic hypogonadism 18 with or without anosmia1Feb 21, 2021
Hypogonadotropic hypogonadism 19 with or without anosmia2Mar 5, 2021
Hypogonadotropic hypogonadism 2 with or without anosmia3Oct 2, 2023
Hypogonadotropic hypogonadism 21 with or without anosmia1Feb 21, 2021
Hypogonadotropic hypogonadism 26 with or without anosmia1Oct 2, 2023
Hypogonadotropic hypogonadism 5 with or without anosmia7Mar 5, 2021
Hypogonadotropic hypogonadism 6 with or without anosmia1Mar 5, 2021
Hypogonadotropic hypogonadism 7 with or without anosmia2Mar 5, 2021
Hypogonadotropic hypogonadism 8 with or without anosmia1Feb 21, 2021
Hypohidrotic X-linked ectodermal dysplasia1Feb 21, 2021
Hypokalemic periodic paralysis, type 15Oct 2, 2023
Hypokalemic periodic paralysis, type 21Feb 21, 2021
Hypomyelinating leukodystrophy 102Mar 5, 2021
Hypomyelinating leukodystrophy 113Mar 5, 2021
Hypomyelinating leukodystrophy 127Feb 19, 2023
Hypomyelinating leukodystrophy 131Feb 21, 2021
Hypomyelinating leukodystrophy 21Oct 16, 2017
Hypomyelinating leukodystrophy 31Oct 2, 2023
Hypomyelinating leukodystrophy 43Feb 21, 2021
Hypomyelinating leukodystrophy 64Oct 2, 2023
Hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism9Oct 2, 2023
Hypomyelinating leukodystrophy 910Feb 19, 2023
Hypomyelination and Congenital Cataract2Feb 21, 2021
Hypomyelination with brain stem and spinal cord involvement and leg spasticity4Mar 5, 2021
Hypoparathyroidism, deafness, renal disease syndrome2Oct 2, 2023
Hypophosphatasia1Oct 2, 2023
Hypophosphatemic nephrolithiasis/osteoporosis 22Feb 19, 2023
Hypophosphatemic rickets, X-linked recessive1Feb 21, 2021
Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome3Mar 5, 2021
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration2Mar 5, 2021
Hypothyroidism due to TSH receptor mutations1Oct 2, 2023
Hypothyroidism, congenital, nongoitrous, 22Feb 21, 2021
Hypothyroidism, congenital, nongoitrous, 91Feb 21, 2021
Hypotonia2Nov 12, 2016
Hypotonia with lactic acidemia and hyperammonemia3Mar 5, 2021
Hypotonia, ataxia, and delayed development syndrome7Feb 19, 2023
Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome2Feb 19, 2023
Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities1Feb 21, 2021
Hypotonia, infantile, with psychomotor retardation and characteristic facies 12Mar 5, 2021
Hypotonia, infantile, with psychomotor retardation and characteristic facies 235Oct 2, 2023
Hypotonia, infantile, with psychomotor retardation and characteristic facies 313Mar 5, 2021
Hypotrichosis 131Feb 21, 2021
Hypotrichosis 21Feb 21, 2021
Hypotrichosis 81Nov 14, 2016
Hypouricemia, renal, 21Nov 14, 2016
IFAP syndrome 1, with or without BRESHECK syndrome3Oct 2, 2023
IFAP syndrome 21Oct 2, 2023
IL21-related infantile inflammatory bowel disease1Mar 5, 2021
IMAGe syndrome3Oct 2, 2023
Ichthyosis1Nov 14, 2016
Ichthyosis vulgaris19Dec 14, 2023
Ichthyosis, congenital, autosomal recessive 122Feb 21, 2021
Idiopathic basal ganglia calcification 11Feb 19, 2023
IgA nephropathy, susceptibility to, 31Feb 21, 2021
IgE responsiveness, atopic1Feb 19, 2023
Imerslund-Grasbeck syndrome type 17Mar 5, 2021
Immunodeficiency 1047Mar 5, 2021
Immunodeficiency 144Mar 5, 2021
Immunodeficiency 14b, autosomal recessive1Oct 2, 2023
Immunodeficiency 15a1Feb 21, 2021
Immunodeficiency 182Mar 5, 2021
Immunodeficiency 191Mar 5, 2021
Immunodeficiency 234Mar 5, 2021
Immunodeficiency 358Oct 2, 2023
Immunodeficiency 362Oct 2, 2023
Immunodeficiency 391Feb 21, 2021
Immunodeficiency 451Feb 21, 2021
Immunodeficiency 493Mar 5, 2021
Immunodeficiency 514Mar 5, 2021
Immunodeficiency 576Feb 19, 2023
Immunodeficiency 601Feb 21, 2021
Immunodeficiency 63 with lymphoproliferation and autoimmunity1Feb 21, 2021
Immunodeficiency 671Mar 5, 2021
Immunodeficiency 72 with autoinflammation1Feb 19, 2023
Immunodeficiency 754Oct 2, 2023
Immunodeficiency 811Dec 14, 2023
Immunodeficiency 87 and autoimmunity2Feb 19, 2023
Immunodeficiency 951Oct 2, 2023
Immunodeficiency due to CD25 deficiency3Mar 5, 2021
Immunodeficiency due to MASP-2 deficiency2Mar 5, 2021
Immunodeficiency due to ficolin3 deficiency1Feb 21, 2021
Immunodeficiency, common variable, 11Feb 21, 2021
Immunodeficiency, common variable, 102Feb 21, 2021
Immunodeficiency, common variable, 122Feb 21, 2021
Immunodeficiency, common variable, 143Mar 5, 2021
Immunodeficiency, common variable, 28Oct 2, 2023
Immunodeficiency, common variable, 32Mar 5, 2021
Immunodeficiency, common variable, 712Feb 19, 2023
Immunodeficiency, developmental delay, and hypohomocysteinemia1Mar 5, 2021
Immunodeficiency-centromeric instability-facial anomalies syndrome 12Mar 5, 2021
Immunodeficiency-centromeric instability-facial anomalies syndrome 24Feb 19, 2023
Immunodeficiency-centromeric instability-facial anomalies syndrome 42Mar 5, 2021
Immunoglobulin A deficiency 23Mar 5, 2021
Immunoglobulin-mediated membranoproliferative glomerulonephritis2Mar 5, 2021
Immunoskeletal dysplasia with neurodevelopmental abnormalities1Mar 5, 2021
Inborn glycerol kinase deficiency2Feb 19, 2023
Infantile GM1 gangliosidosis7Mar 5, 2021
Infantile bilateral striatal necrosis1Feb 21, 2021
Infantile cerebellar-retinal degeneration7Oct 2, 2023
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly6Oct 2, 2023
Infantile convulsions and choreoathetosis2Feb 21, 2021
Infantile cortical hyperostosis3Feb 21, 2021
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency1Feb 21, 2021
Infantile hypophosphatasia1Mar 12, 2023
Infantile liver failure syndrome 15Feb 21, 2021
Infantile liver failure syndrome 28Mar 12, 2023
Infantile liver failure syndrome 32Dec 7, 2023
Infantile muscular hypotonia7Jun 19, 2015
Infantile nephronophthisis3Mar 5, 2021
Infantile neuroaxonal dystrophy15Mar 12, 2023
Infantile onset spinocerebellar ataxia5Oct 2, 2023
Infantile-onset X-linked spinal muscular atrophy1Mar 5, 2021
Infantile-onset ascending hereditary spastic paralysis1Feb 19, 2023
Infantile-onset periodic fever-panniculitis-dermatosis syndrome2Feb 21, 2021
Inflammatory bowel disease 12Mar 5, 2021
Inflammatory bowel disease 132Mar 5, 2021
Inflammatory bowel disease 253Mar 5, 2021
Inflammatory bowel disease 281Feb 21, 2021
Inflammatory bowel disease, immunodeficiency, and encephalopathy1Feb 21, 2021
Inflammatory skin and bowel disease, neonatal, 12Mar 5, 2021
Inflammatory skin and bowel disease, neonatal, 22Dec 7, 2023
Insulin-dependent diabetes mellitus secretory diarrhea syndrome5Dec 7, 2023
Insulin-resistant diabetes mellitus AND acanthosis nigricans1Mar 5, 2021
Intellectual developmental disorder 591Feb 19, 2023
Intellectual developmental disorder 615Oct 2, 2023
Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature3Feb 19, 2023
Intellectual developmental disorder with autism and macrocephaly13Dec 14, 2023
Intellectual developmental disorder with autistic features and language delay, with or without seizures2Feb 19, 2023
Intellectual developmental disorder with cardiac defects and dysmorphic facies9Feb 19, 2023
Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities8Feb 19, 2023
Intellectual developmental disorder with dysmorphic facies and ptosis10Dec 14, 2023
Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies5Mar 5, 2021
Intellectual developmental disorder with gastrointestinal difficulties and high pain threshold3Mar 5, 2021
Intellectual developmental disorder with hypotonia and behavioral abnormalities1Feb 19, 2023
Intellectual developmental disorder with impaired language and dysmorphic facies1Feb 19, 2023
Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism2Oct 2, 2023
Intellectual developmental disorder with macrocephaly, seizures, and speech delay1Feb 19, 2023
Intellectual developmental disorder with neuropsychiatric features9Mar 5, 2021
Intellectual developmental disorder with or without epilepsy or cerebellar ataxia5Oct 2, 2023
Intellectual developmental disorder with poor growth and with or without seizures or ataxia1Feb 19, 2023
Intellectual developmental disorder with seizures and language delay3Oct 2, 2023
Intellectual developmental disorder with short stature and behavioral abnormalities3Feb 19, 2023
Intellectual developmental disorder with short stature and variable skeletal anomalies1Feb 21, 2021
Intellectual developmental disorder with speech delay, autism, and dysmorphic facies6Oct 2, 2023
Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities8Oct 2, 2023
Intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type1Feb 19, 2023
Intellectual developmental disorder, autosomal dominant 63, with macrocephaly3Feb 19, 2023
Intellectual developmental disorder, autosomal dominant 641Oct 2, 2023
Intellectual developmental disorder, autosomal dominant 651Dec 14, 2023
Intellectual developmental disorder, autosomal dominant 662Dec 14, 2023
Intellectual developmental disorder, autosomal dominant 681Dec 14, 2023
Intellectual developmental disorder, autosomal dominant 701Oct 2, 2023
Intellectual developmental disorder, autosomal recessive 672Mar 12, 2023
Intellectual developmental disorder, autosomal recessive 687Oct 2, 2023
Intellectual developmental disorder, autosomal recessive 693Feb 21, 2021
Intellectual developmental disorder, autosomal recessive 701Feb 21, 2021
Intellectual developmental disorder, autosomal recessive 711Feb 19, 2023
Intellectual developmental disorder, autosomal recessive 746Mar 5, 2021
Intellectual disability31Jul 17, 2021
Intellectual disability, X-linked 16Feb 19, 2023
Intellectual disability, X-linked 1005Feb 19, 2023
Intellectual disability, X-linked 1013Dec 14, 2023
Intellectual disability, X-linked 10213Oct 2, 2023
Intellectual disability, X-linked 1033Feb 19, 2023
Intellectual disability, X-linked 1048Feb 19, 2023
Intellectual disability, X-linked 1052Feb 21, 2021
Intellectual disability, X-linked 1066Dec 14, 2023
Intellectual disability, X-linked 1072Feb 21, 2021
Intellectual disability, X-linked 301Mar 5, 2021
Intellectual disability, X-linked 462Feb 21, 2021
Intellectual disability, X-linked 493Feb 19, 2023
Intellectual disability, X-linked 502Feb 19, 2023
Intellectual disability, X-linked 612Oct 2, 2023
Intellectual disability, X-linked 632Oct 2, 2023
Intellectual disability, X-linked 902Oct 2, 2023
Intellectual disability, X-linked 912Mar 5, 2021
Intellectual disability, X-linked 938Oct 2, 2023
Intellectual disability, X-linked 961Feb 21, 2021
Intellectual disability, X-linked 974Oct 2, 2023
Intellectual disability, X-linked 9914Dec 14, 2023
Intellectual disability, X-linked 99, syndromic, female-restricted5Dec 14, 2023
Intellectual disability, X-linked syndromic, Turner type7Oct 2, 2023
Intellectual disability, X-linked, syndromic 336Oct 2, 2023
Intellectual disability, X-linked, syndromic, 352Mar 5, 2021
Intellectual disability, X-linked, syndromic, Bain type1Dec 14, 2023
Intellectual disability, X-linked, syndromic, Houge type3Feb 21, 2021
Intellectual disability, X-linked, with or without seizures, arx-related1Feb 21, 2021
Intellectual disability, X-linked, with panhypopituitarism4Oct 2, 2023
Intellectual disability, anterior maxillary protrusion, and strabismus3Mar 5, 2021
Intellectual disability, autosomal dominant 110Mar 5, 2021
Intellectual disability, autosomal dominant 101Oct 2, 2023
Intellectual disability, autosomal dominant 112Feb 21, 2021
Intellectual disability, autosomal dominant 138Oct 2, 2023
Intellectual disability, autosomal dominant 1422Oct 2, 2023
Intellectual disability, autosomal dominant 157Feb 19, 2023
Intellectual disability, autosomal dominant 1612Feb 19, 2023
Intellectual disability, autosomal dominant 203Mar 5, 2021
Intellectual disability, autosomal dominant 224Mar 5, 2021
Intellectual disability, autosomal dominant 248Feb 19, 2023
Intellectual disability, autosomal dominant 274Mar 5, 2021
Intellectual disability, autosomal dominant 2913Oct 2, 2023
Intellectual disability, autosomal dominant 37Mar 5, 2021
Intellectual disability, autosomal dominant 305Feb 19, 2023
Intellectual disability, autosomal dominant 332Mar 5, 2021
Intellectual disability, autosomal dominant 383Mar 5, 2021
Intellectual disability, autosomal dominant 394Oct 2, 2023
Intellectual disability, autosomal dominant 41Mar 5, 2021
Intellectual disability, autosomal dominant 403Mar 5, 2021
Intellectual disability, autosomal dominant 413Feb 21, 2021
Intellectual disability, autosomal dominant 425Feb 19, 2023
Intellectual disability, autosomal dominant 4310Mar 5, 2021
Intellectual disability, autosomal dominant 4512Feb 19, 2023
Intellectual disability, autosomal dominant 463Mar 5, 2021
Intellectual disability, autosomal dominant 4716Feb 19, 2023
Intellectual disability, autosomal dominant 484Oct 2, 2023
Intellectual disability, autosomal dominant 524Feb 19, 2023
Intellectual disability, autosomal dominant 504Oct 2, 2023
Intellectual disability, autosomal dominant 512Mar 5, 2021
Intellectual disability, autosomal dominant 5218Oct 2, 2023
Intellectual disability, autosomal dominant 55, with seizures2Mar 5, 2021
Intellectual disability, autosomal dominant 563Feb 19, 2023
Intellectual disability, autosomal dominant 571Mar 14, 2019
Intellectual disability, autosomal dominant 582Feb 21, 2021
Intellectual disability, autosomal dominant 610Oct 2, 2023
Intellectual disability, autosomal dominant 811Oct 2, 2023
Intellectual disability, autosomal dominant 925Dec 14, 2023
Intellectual disability, autosomal recessive 19Oct 2, 2023
Intellectual disability, autosomal recessive 121Mar 5, 2021
Intellectual disability, autosomal recessive 1321Oct 2, 2023
Intellectual disability, autosomal recessive 142Mar 5, 2021
Intellectual disability, autosomal recessive 188Feb 19, 2023
Intellectual disability, autosomal recessive 26Feb 19, 2023
Intellectual disability, autosomal recessive 2711Mar 5, 2021
Intellectual disability, autosomal recessive 315Mar 5, 2021
Intellectual disability, autosomal recessive 344Mar 5, 2021
Intellectual disability, autosomal recessive 427Mar 5, 2021
Intellectual disability, autosomal recessive 435Mar 5, 2021
Intellectual disability, autosomal recessive 447Feb 19, 2023
Intellectual disability, autosomal recessive 454Mar 5, 2021
Intellectual disability, autosomal recessive 465Mar 5, 2021
Intellectual disability, autosomal recessive 4714Feb 19, 2023
Intellectual disability, autosomal recessive 58Feb 19, 2023
Intellectual disability, autosomal recessive 511Mar 5, 2021
Intellectual disability, autosomal recessive 524Mar 5, 2021
Intellectual disability, autosomal recessive 5325Feb 19, 2023
Intellectual disability, autosomal recessive 543Mar 5, 2021
Intellectual disability, autosomal recessive 565Dec 14, 2023
Intellectual disability, autosomal recessive 5712Mar 5, 2021
Intellectual disability, autosomal recessive 589Mar 5, 2021
Intellectual disability, autosomal recessive 593Mar 5, 2021
Intellectual disability, autosomal recessive 69Feb 19, 2023
Intellectual disability, autosomal recessive 601Feb 21, 2021
Intellectual disability, autosomal recessive 6116Mar 5, 2021
Intellectual disability, autosomal recessive 643Mar 5, 2021
Intellectual disability, autosomal recessive 655Mar 5, 2021
Intellectual disability, autosomal recessive 72Feb 19, 2023
Intellectual disability, mild2Aug 17, 2015
Intellectual disability-epilepsy-extrapyramidal syndrome1Aug 21, 2017
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency18Feb 19, 2023
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome8Feb 19, 2023
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome12Oct 2, 2023
Intellectual disability-hypotonic facies syndrome, X-linked, 19Feb 19, 2023
Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome12Dec 14, 2023
Intellectual disability-severe speech delay-mild dysmorphism syndrome7Mar 12, 2023
Intellectual disability-strabismus syndrome7Mar 5, 2021
Interstitial lung disease 25Mar 5, 2021
Interstitial lung disease due to ABCA3 deficiency4Mar 5, 2021
Intestinal hypomagnesemia 13Mar 5, 2021
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency2Dec 6, 2021
Iodotyrosyl coupling defect10Feb 19, 2023
Iris coloboma3Nov 15, 2017
Isolated focal cortical dysplasia type II275Dec 14, 2023
Isolated growth hormone deficiency type IB4Mar 5, 2021
Isolated growth hormone deficiency, type 51Feb 19, 2023
Isolated hyperchlorhidrosis1Feb 21, 2021
Isolated microphthalmia 51Aug 17, 2015
Isovaleryl-CoA dehydrogenase deficiency68Dec 7, 2023
Jackson-Weiss syndrome2Feb 21, 2021
Jawad syndrome3Mar 5, 2021
Jervell and Lange-Nielsen syndrome 21Mar 5, 2021
Johanson-Blizzard syndrome4Feb 19, 2023
Joint laxity, short stature, and myopia4Mar 5, 2021
Joubert syndrome 15Feb 19, 2023
Joubert syndrome 104Feb 19, 2023
Joubert syndrome 133Mar 5, 2021
Joubert syndrome 143Mar 12, 2023
Joubert syndrome 153Mar 5, 2021
Joubert syndrome 1717Mar 1, 2024
Joubert syndrome 181Feb 21, 2021
Joubert syndrome 215Dec 7, 2023
Joubert syndrome 204Mar 5, 2021
Joubert syndrome 2110Feb 19, 2023
Joubert syndrome 236Oct 2, 2023
Joubert syndrome 241Feb 21, 2021
Joubert syndrome 252Mar 5, 2021
Joubert syndrome 262Feb 19, 2023
Joubert syndrome 271Mar 5, 2021
Joubert syndrome 35Feb 19, 2023
Joubert syndrome 302Mar 5, 2021
Joubert syndrome 315Oct 2, 2023
Joubert syndrome 321Feb 10, 2021
Joubert syndrome 332Mar 5, 2021
Joubert syndrome 371Feb 19, 2023
Joubert syndrome 401Feb 19, 2023
Joubert syndrome 54Mar 5, 2021
Joubert syndrome 62Oct 16, 2017
Joubert syndrome 81Mar 5, 2021
Joubert syndrome 95Feb 19, 2023
Joubert syndrome with renal defect52Dec 7, 2023
Junctional epidermolysis bullosa gravis of Herlitz7Feb 19, 2023
Junctional epidermolysis bullosa with pyloric atresia6Oct 2, 2023
Junctional epidermolysis bullosa, non-Herlitz type6Feb 19, 2023
Juvenile arthritis due to defect in LACC11Feb 21, 2021
Juvenile myelomonocytic leukemia360Dec 7, 2023
Juvenile myoclonic epilepsy1Oct 16, 2017
Juvenile nephropathic cystinosis2Sep 27, 2019
Juvenile onset Parkinson disease 19A1Mar 5, 2021
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome41Dec 7, 2023
Juvenile primary lateral sclerosis3Feb 19, 2023
Juvenile retinoschisis9Dec 14, 2023
Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome1Feb 21, 2021
KBG syndrome48Oct 2, 2023
KIF21B-related disorders1Feb 19, 2023
KINSSHIP syndrome2Oct 2, 2023
KLF7-related neurodevelopmental disorder1Feb 19, 2023
KLHL9-related distal myopathy1Feb 19, 2023
Kabuki syndrome 154Dec 14, 2023
Kabuki syndrome 27Oct 2, 2023
Kartagener syndrome1Mar 5, 2021
Karyomegalic interstitial nephritis1Mar 5, 2021
Keipert syndrome1Feb 21, 2021
Kennedy disease1Feb 21, 2021
Keratosis follicularis spinulosa decalvans, X-linked2Oct 2, 2023
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome1Oct 2, 2023
Khan-Khan-Katsanis syndrome2Feb 19, 2023
Kleefstra syndrome 113Oct 2, 2023
Kleefstra syndrome 212Oct 2, 2023
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome9Mar 12, 2023
Klippel-Feil syndrome 1, autosomal dominant2Mar 5, 2021
Knobloch syndrome3Mar 5, 2021
Kohlschutter-Tonz syndrome-like1Dec 14, 2023
Koolen-de Vries syndrome11Dec 14, 2023
Kostmann syndrome3Feb 21, 2021
Kufor-Rakeb syndrome8Feb 19, 2023
L-2-hydroxyglutaric aciduria4Mar 5, 2021
LAMB2-related infantile-onset nephrotic syndrome7Oct 2, 2023
LEOPARD syndrome 119Dec 14, 2023
LEOPARD syndrome 31Feb 21, 2021
LIPE-related familial partial lipodystrophy3Feb 21, 2021
Lafora disease5Oct 2, 2023
Lamb-Shaffer syndrome9Oct 2, 2023
Landau-Kleffner syndrome15Dec 14, 2023
Langer mesomelic dysplasia syndrome2Mar 5, 2021
Larsen syndrome1Feb 19, 2023
Larsen-like syndrome, B3GAT3 type2Oct 2, 2023
Laryngo-onycho-cutaneous syndrome1Feb 19, 2023
Laurence-Moon syndrome2Feb 21, 2021
Leber congenital amaurosis 11Feb 21, 2021
Leber congenital amaurosis 1363Dec 7, 2023
Leber congenital amaurosis 151Mar 5, 2021
Leber congenital amaurosis 172Mar 12, 2023
Leber congenital amaurosis 293Dec 7, 2023
Leber congenital amaurosis 31Mar 5, 2021
Leber congenital amaurosis 541Dec 7, 2023
Leber congenital amaurosis 8141Dec 7, 2023
Leber congenital amaurosis with early-onset deafness1Feb 19, 2023
Left ventricular noncompaction7Jun 19, 2015
Left ventricular noncompaction 14Dec 14, 2023
Left ventricular noncompaction 1021Dec 14, 2023
Left ventricular noncompaction 23Feb 19, 2023
Left ventricular noncompaction 74Oct 2, 2023
Left ventricular noncompaction 82Oct 2, 2023
Legius syndrome3Mar 5, 2021
Leigh syndrome32Mar 5, 2021
Lenz-Majewski hyperostosis syndrome3Oct 2, 2023
Leri-Weill dyschondrosteosis1Nov 14, 2016
Lethal Kniest-like syndrome13Oct 2, 2023
Lethal arthrogryposis-anterior horn cell disease syndrome1Mar 5, 2021
Lethal congenital contracture syndrome 111Feb 21, 2021
Lethal congenital contracture syndrome 61Mar 5, 2021
Lethal congenital contracture syndrome 72Mar 5, 2021
Lethal congenital contracture syndrome 91Feb 21, 2021
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome3Mar 5, 2021
Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome8Mar 5, 2021
Lethal multiple pterygium syndrome6Oct 2, 2023
Lethal occipital encephalocele-skeletal dysplasia syndrome1Feb 10, 2021
Lethal polymalformative syndrome, Boissel type1Feb 21, 2021
Lethal tight skin contracture syndrome3Feb 21, 2021
Leukocyte adhesion deficiency 11Mar 5, 2021
Leukocyte adhesion deficiency 32Feb 21, 2021
Leukocyte adhesion deficiency type II6Mar 5, 2021
Leukodystrophy and acquired microcephaly with or without dystonia;12Mar 5, 2021
Leukodystrophy, hypomyelinating, 141Feb 21, 2021
Leukodystrophy, hypomyelinating, 158Feb 19, 2023
Leukodystrophy, hypomyelinating, 162Feb 21, 2021
Leukodystrophy, hypomyelinating, 171Feb 19, 2023
Leukoencephalopathy3Feb 21, 2020
Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome3Feb 19, 2023
Leukoencephalopathy with mild cerebellar ataxia and white matter edema2Mar 5, 2021
Leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate2Feb 21, 2021
Leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome1Oct 2, 2023
Leukoencephalopathy, diffuse hereditary, with spheroids 11Oct 2, 2023
Leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome1Feb 19, 2023
Leukoencephalopathy, progressive, with ovarian failure2Feb 19, 2023
Leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome14Mar 5, 2021
Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome11Dec 14, 2023
Levy-Hollister syndrome1Mar 14, 2019
Li-Fraumeni syndrome 19Oct 2, 2023
Li-Fraumeni syndrome 211Feb 11, 2022
Lichtenstein-Knorr syndrome1Feb 19, 2023
Limb-girdle muscular dystrophy due to POMK deficiency1Dec 14, 2023
Linear skin defects with multiple congenital anomalies 21Feb 21, 2021
Lipase deficiency, combined3Feb 21, 2021
Lipid proteinosis1Feb 21, 2021
Lipoic acid synthetase deficiency3Feb 21, 2021
Lipoyl transferase 1 deficiency2Oct 16, 2017
Lissencephaly 43Mar 5, 2021
Lissencephaly 6 with microcephaly1Mar 5, 2021
Lissencephaly 82Mar 5, 2021
Lissencephaly 9 with complex brainstem malformation11Dec 14, 2023
Lissencephaly due to LIS1 mutation3Oct 16, 2017
Lissencephaly due to TUBA1A mutation11Dec 14, 2023
Lissencephaly type 1 due to doublecortin gene mutation2Feb 21, 2021
Loeys-Dietz syndrome 14Feb 19, 2023
Loeys-Dietz syndrome 24Feb 21, 2021
Loeys-Dietz syndrome 44Feb 19, 2023
Long QT syndrome 17Dec 14, 2023
Long QT syndrome 117Feb 19, 2023
Long QT syndrome 121Feb 21, 2021
Long QT syndrome 22Feb 19, 2023
Long QT syndrome 32Feb 19, 2023
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency56Dec 7, 2023
Long qt syndrome 83Oct 2, 2023
Lopes-Maciel-Rodan syndrome8Oct 2, 2023
Lowe syndrome1Oct 16, 2017
Lung cancer6Feb 10, 2021
Lung disease, immunodeficiency, and chromosome breakage syndrome;1Mar 5, 2021
Luscan-Lumish syndrome15Oct 2, 2023
Lymphangiomyomatosis3Mar 5, 2021
Lymphatic malformation 66Oct 2, 2023
Lymphoproliferative syndrome 12Feb 21, 2021
Lynch syndrome 1352Dec 7, 2023
Lynch syndrome 4317Dec 14, 2023
Lynch syndrome 57Dec 6, 2021
Lysinuric protein intolerance56Dec 7, 2023
Lysosomal acid lipase deficiency1Feb 19, 2023
MASA syndrome3Feb 21, 2021
MEGF10-related myopathy4Oct 2, 2023
MEGF8-related Carpenter syndrome13Oct 2, 2023
MEHMO syndrome1Mar 5, 2021
MGAT2-congenital disorder of glycosylation2Mar 5, 2021
MHC class I deficiency6Oct 2, 2023
MHC class II deficiency11Feb 19, 2023
MIRAGE syndrome4Feb 19, 2023
MOGS-congenital disorder of glycosylation3Mar 5, 2021
MPDU1-congenital disorder of glycosylation2Mar 5, 2021
MPI-congenital disorder of glycosylation50Dec 7, 2023
MYH6-related cardiac defects4Oct 2, 2023
MYH7-related skeletal myopathy15Dec 14, 2023
MYPN-related myopathy1Oct 2, 2023
Macrocephaly, dysmorphic facies, and psychomotor retardation17Oct 2, 2023
Macrocephaly-autism syndrome5Feb 21, 2021
Macrocephaly-developmental delay syndrome5Feb 19, 2023
Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome6Oct 2, 2023
Macrocephaly/megalencephaly syndrome, autosomal recessive1Mar 5, 2021
Macrocytic dyserythropoietic anemia2Aug 17, 2015
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss4Oct 2, 2023
Macrothrombocytopenia, isolated, 1, autosomal dominant2Mar 5, 2021
Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome2Feb 19, 2023
Macular corneal dystrophy2Feb 21, 2021
Macular degeneration, X-linked atrophic1Feb 19, 2023
Macular degeneration, age-related, 31Mar 14, 2019
Macular degeneration, early-onset1Feb 21, 2021
Macular dystrophy with central cone involvement1Mar 5, 2021
Malan overgrowth syndrome2Feb 21, 2021
Malaria, susceptibility to33Dec 7, 2023
Malignant hyperthermia, susceptibility to, 118Dec 14, 2023
Malignant tumor of esophagus1Mar 5, 2021
Malignant tumor of prostate1Feb 19, 2023
Malignant tumor of urinary bladder58Dec 7, 2023
Mandibular hypoplasia-deafness-progeroid syndrome6Feb 11, 2022
Mandibuloacral dysplasia with type A lipodystrophy1Feb 21, 2021
Mandibuloacral dysplasia with type B lipodystrophy3Feb 19, 2023
Mandibulofacial dysostosis-microcephaly syndrome8Dec 14, 2023
Mannose-binding lectin deficiency1Feb 21, 2021
Maple syrup urine disease173Dec 7, 2023
Marden-Walker syndrome3Feb 19, 2023
Marfan syndrome14Dec 14, 2023
Marinesco-Sjögren syndrome5Mar 5, 2021
Marshall syndrome1Feb 19, 2023
Marshall-Smith syndrome1Feb 19, 2023
Martsolf syndrome3Mar 5, 2021
Mast syndrome1Feb 21, 2021
Matthew-Wood syndrome2Mar 5, 2021
Maturity-onset diabetes of the young type 11Mar 14, 2019
Maturity-onset diabetes of the young type 112Feb 19, 2023
Maturity-onset diabetes of the young type 24Feb 19, 2023
Maturity-onset diabetes of the young type 32Oct 2, 2023
Maturity-onset diabetes of the young type 71Feb 21, 2021
Maturity-onset diabetes of the young type 82Mar 5, 2021
McCune-Albright syndrome1Feb 21, 2021
Meckel syndrome, type 12Feb 21, 2021
Meckel syndrome, type 112Feb 21, 2021
Meckel syndrome, type 34Mar 12, 2023
Meckel syndrome, type 41Feb 21, 2021
Meckel syndrome, type 54Mar 5, 2021
Meckel syndrome, type 65Feb 21, 2021
Meckel syndrome, type 82Feb 21, 2021
Meckel syndrome, type 92Mar 5, 2021
Medium-chain acyl-coenzyme A dehydrogenase deficiency137Dec 14, 2023
Medulloblastoma1Dec 6, 2021
Meester-Loeys syndrome1Mar 5, 2021
Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations5Oct 2, 2023
Megaconial type congenital muscular dystrophy3Feb 19, 2023
Megalencephalic leukoencephalopathy with subcortical cysts 150Dec 7, 2023
Megalencephalic leukoencephalopathy with subcortical cysts 2A3Mar 5, 2021
Megalencephaly-capillary malformation-polymicrogyria syndrome2Feb 21, 2021
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 12Feb 19, 2023
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 32Mar 5, 2021
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness1Mar 5, 2021
Meier-Gorlin syndrome3Jun 23, 2015
Meier-Gorlin syndrome 14Feb 19, 2023
Meier-Gorlin syndrome 31Mar 5, 2021
Meier-Gorlin syndrome 41Feb 21, 2021
Meier-Gorlin syndrome 72Mar 5, 2021
Meier-Gorlin syndrome 81Mar 5, 2021
Melanoma and neural system tumor syndrome70Dec 7, 2023
Melanoma, cutaneous malignant, susceptibility to, 162Dec 7, 2023
Melanoma, cutaneous malignant, susceptibility to, 81Dec 7, 2023
Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency3Mar 5, 2021
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency4Feb 19, 2023
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency5Mar 5, 2021
Menke-Hennekam syndrome 14Feb 21, 2021
Menke-Hennekam syndrome 21Feb 21, 2021
Menkes kinky-hair syndrome9Dec 7, 2023
Merosin deficient congenital muscular dystrophy184Dec 7, 2023
Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression1Feb 21, 2021
Metachondromatosis15Dec 14, 2023
Metachromatic leukodystrophy12Mar 5, 2021
Metaphyseal anadysplasia 22Feb 21, 2021
Metaphyseal chondrodysplasia, Jansen type2Feb 19, 2023
Metaphyseal chondrodysplasia, Schmid type1Feb 21, 2021
Metaphyseal chondrodysplasia, Spahr type1Feb 21, 2021
Methylcobalamin deficiency type cblE3Feb 19, 2023
Methylcobalamin deficiency type cblG1Mar 5, 2021
Methylmalonate semialdehyde dehydrogenase deficiency1Mar 5, 2021
Methylmalonic acidemia with homocystinuria, type cblJ1Feb 19, 2023
Methylmalonic acidemia with homocystinuria, type cblX7Feb 19, 2023
Methylmalonic aciduria and homocystinuria type cblD25Dec 7, 2023
Methylmalonic aciduria and homocystinuria type cblF5Oct 2, 2023
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency5Mar 5, 2021
Methylmalonic aciduria, cblA type42Dec 7, 2023
Methylmalonic aciduria, cblB type28Dec 7, 2023
Methylmalonic aciduria, type cblc1Dec 14, 2023
Mevalonic aciduria3Feb 21, 2021
Microangiopathy and leukoencephalopathy, pontine, autosomal dominant1Oct 7, 2022
Microcephalic osteodysplastic primordial dwarfism type II12Feb 19, 2023
Microcephalic primordial dwarfism due to RTTN deficiency15Feb 19, 2023
Microcephalic primordial dwarfism due to ZNF335 deficiency4Feb 21, 2021
Microcephalic primordial dwarfism, Alazami type1Feb 21, 2021
Microcephaly 1, primary, autosomal recessive6Mar 5, 2021
Microcephaly 11, primary, autosomal recessive2Mar 5, 2021
Microcephaly 13, primary, autosomal recessive4Mar 5, 2021
Microcephaly 15, primary, autosomal recessive1Feb 21, 2021
Microcephaly 16, primary, autosomal recessive2Feb 21, 2021
Microcephaly 17, primary, autosomal recessive9Feb 19, 2023
Microcephaly 18, primary, autosomal dominant8Feb 19, 2023
Microcephaly 2, primary, autosomal recessive, with or without cortical malformations14Oct 2, 2023
Microcephaly 20, primary, autosomal recessive6Feb 19, 2023
Microcephaly 21, primary, autosomal recessive3Feb 21, 2021
Microcephaly 22, primary, autosomal recessive6Mar 5, 2021
Microcephaly 23, primary, autosomal recessive2Feb 21, 2021
Microcephaly 24, primary, autosomal recessive1Feb 21, 2021
Microcephaly 25, primary, autosomal recessive1Feb 21, 2021
Microcephaly 27, primary, autosomal dominant1Oct 2, 2023
Microcephaly 3, primary, autosomal recessive12Mar 5, 2021
Microcephaly 4, primary, autosomal recessive9Mar 5, 2021
Microcephaly 5, primary, autosomal recessive21Mar 5, 2021
Microcephaly 6, primary, autosomal recessive4Mar 5, 2021
Microcephaly 7, primary, autosomal recessive5Mar 5, 2021
Microcephaly 8, primary, autosomal recessive4Mar 5, 2021
Microcephaly 9, primary, autosomal recessive4Oct 2, 2023
Microcephaly and chorioretinopathy 111Mar 5, 2021
Microcephaly and chorioretinopathy 23Mar 5, 2021
Microcephaly and chorioretinopathy 32Feb 21, 2021
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability8Feb 19, 2023
Microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum2Feb 21, 2021
Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome1Feb 21, 2021
Microcephaly, growth deficiency, seizures, and brain malformations2Dec 14, 2023
Microcephaly, growth restriction, and increased sister chromatid exchange 22Feb 19, 2023
Microcephaly, normal intelligence and immunodeficiency7Mar 12, 2023
Microcephaly, short stature, and impaired glucose metabolism 12Feb 21, 2021
Microcephaly, short stature, and limb abnormalities3Mar 5, 2021
Microcephaly-capillary malformation syndrome5Mar 5, 2021
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome8Feb 19, 2023
Microcephaly-micromelia syndrome1Mar 12, 2023
Microcephaly-thin corpus callosum-intellectual disability syndrome2Mar 5, 2021
Microcytic anemia2Feb 21, 2021
Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome20Feb 19, 2023
Microphthalmia, isolated, with coloboma 31Feb 21, 2021
Microphthalmia, isolated, with coloboma 92Mar 5, 2021
Microphthalmia, syndromic 122Feb 19, 2023
Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis1Oct 2, 2023
Migraine, familial hemiplegic, 12Oct 16, 2017
Migraine, familial hemiplegic, 23Feb 19, 2023
Migraine, familial hemiplegic, 33Feb 21, 2021
Mild global developmental delay1Mar 19, 2021
Miller syndrome1Feb 19, 2023
Mirror movements 12Mar 5, 2021
Mismatch repair cancer syndrome 16Dec 6, 2021
Mitchell syndrome18Dec 7, 2023
Mitochondrial DNA deletion syndrome with progressive myopathy1Feb 21, 2021
Mitochondrial DNA depletion syndrome 138Dec 7, 2023
Mitochondrial DNA depletion syndrome 112Feb 19, 2023
Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant1Mar 5, 2021
Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive1Dec 14, 2023
Mitochondrial DNA depletion syndrome 1314Oct 2, 2023
Mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)1Mar 5, 2021
Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)1Feb 19, 2023
Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)2Oct 2, 2023
Mitochondrial DNA depletion syndrome 4b9Sep 27, 2019
Mitochondrial DNA depletion syndrome 8a8Mar 12, 2023
Mitochondrial DNA depletion syndrome 96Feb 19, 2023
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria4Dec 14, 2023
Mitochondrial DNA depletion syndrome, myopathic form3Feb 21, 2021
Mitochondrial complex 1 deficiency, nuclear type 111Feb 19, 2023
Mitochondrial complex 1 deficiency, nuclear type 144Oct 2, 2023
Mitochondrial complex 1 deficiency, nuclear type 151Feb 21, 2021
Mitochondrial complex 1 deficiency, nuclear type 1644Dec 7, 2023
Mitochondrial complex 1 deficiency, nuclear type 171Feb 21, 2021
Mitochondrial complex 1 deficiency, nuclear type 182Mar 12, 2023
Mitochondrial complex 1 deficiency, nuclear type 193Feb 19, 2023
Mitochondrial complex 1 deficiency, nuclear type 21Dec 14, 2023
Mitochondrial complex 1 deficiency, nuclear type 223Dec 14, 2023
Mitochondrial complex 1 deficiency, nuclear type 231Feb 21, 2021
Mitochondrial complex 1 deficiency, nuclear type 251Feb 21, 2021
Mitochondrial complex 1 deficiency, nuclear type 264Feb 19, 2023
Mitochondrial complex 1 deficiency, nuclear type 282Dec 14, 2023
Mitochondrial complex 1 deficiency, nuclear type 291Feb 21, 2021
Mitochondrial complex 1 deficiency, nuclear type 32Feb 19, 2023
Mitochondrial complex 1 deficiency, nuclear type 301Feb 21, 2021
Mitochondrial complex 1 deficiency, nuclear type 313Feb 21, 2021
Mitochondrial complex 1 deficiency, nuclear type 342Feb 19, 2023
Mitochondrial complex 1 deficiency, nuclear type 372Dec 14, 2023
Mitochondrial complex 1 deficiency, nuclear type 48Dec 14, 2023
Mitochondrial complex 1 deficiency, nuclear type 55Oct 2, 2023
Mitochondrial complex 1 deficiency, nuclear type 61Feb 21, 2021
Mitochondrial complex 1 deficiency, nuclear type 72Feb 19, 2023
Mitochondrial complex 1 deficiency, nuclear type 82Feb 19, 2023
Mitochondrial complex 1 deficiency, nuclear type 912Dec 7, 2023
Mitochondrial complex 2 deficiency, nuclear type 325Dec 7, 2023
Mitochondrial complex 4 deficiency, nuclear type 111Feb 19, 2023
Mitochondrial complex 4 deficiency, nuclear type 32Oct 2, 2023
Mitochondrial complex 4 deficiency, nuclear type 44Feb 19, 2023
Mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 61Feb 21, 2021
Mitochondrial complex I deficiency5Oct 16, 2017
Mitochondrial complex I deficiency, nuclear type 156Dec 7, 2023
Mitochondrial complex II deficiency, nuclear type 16Mar 5, 2021
Mitochondrial complex III deficiency nuclear type 15Mar 5, 2021
Mitochondrial complex III deficiency nuclear type 25Feb 19, 2023
Mitochondrial complex III deficiency nuclear type 42Mar 5, 2021
Mitochondrial complex III deficiency nuclear type 53Mar 5, 2021
Mitochondrial complex III deficiency nuclear type 71Mar 5, 2021
Mitochondrial complex III deficiency nuclear type 81Feb 21, 2021
Mitochondrial complex IV deficiency, nuclear type 116Feb 19, 2023
Mitochondrial complex IV deficiency, nuclear type 5, French-Canadian1Dec 14, 2023
Mitochondrial complex V (ATP synthase) deficiency nuclear type 22Feb 19, 2023
Mitochondrial complex V (ATP synthase) deficiency, nuclear type 14Mar 5, 2021
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency10Oct 2, 2023
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome4Mar 5, 2021
Mitochondrial myopathy-lactic acidosis-deafness syndrome4Feb 19, 2023
Mitochondrial pyruvate carrier deficiency1Feb 21, 2021
Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency8Feb 19, 2023
Mitochondrial trifunctional protein deficiency42Dec 7, 2023
Mitochondrial trifunctional protein deficiency 22Dec 14, 2023
Mitral valve prolapse, myxomatous 210Feb 19, 2023
Miyoshi muscular dystrophy 1214Dec 7, 2023
Miyoshi muscular dystrophy 33Mar 5, 2021
Moderate global developmental delay1Dec 6, 2020
Monocytopenia with susceptibility to infections2Mar 5, 2021
Mosaic variegated aneuploidy syndrome 15Feb 21, 2021
Mosaic variegated aneuploidy syndrome 211Feb 11, 2022
Mosaic variegated aneuploidy syndrome 31Mar 5, 2021
Motor delay3Nov 15, 2017
Mowat-Wilson syndrome20Oct 2, 2023
Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome1Apr 1, 2019
Moyamoya disease 22Mar 5, 2021
Moyamoya disease with early-onset achalasia2Mar 5, 2021
Mucolipidosis type II9Mar 5, 2021
Mucolipidosis type IV10Oct 7, 2022
Mucopolysaccharidosis type 12Oct 2, 2023
Mucopolysaccharidosis type 669Dec 7, 2023
Mucopolysaccharidosis type 72Feb 21, 2021
Mucopolysaccharidosis, MPS-I-S2Feb 21, 2021
Mucopolysaccharidosis, MPS-II3Feb 19, 2023
Mucopolysaccharidosis, MPS-III-A78Dec 7, 2023
Mucopolysaccharidosis, MPS-III-B8Oct 2, 2023
Mucopolysaccharidosis, MPS-III-C2Feb 21, 2021
Mucopolysaccharidosis, MPS-III-D2Feb 21, 2021
Mucopolysaccharidosis, MPS-IV-A3Mar 5, 2021
Mucopolysaccharidosis, MPS-IV-B2Mar 14, 2019
Mucopolysaccharidosis-plus syndrome2Feb 21, 2021
Muenke syndrome1Mar 14, 2019
Muir-Torré syndrome3Feb 21, 2021
Mulibrey nanism syndrome41Dec 7, 2023
Mullegama-Klein-Martinez syndrome4Oct 2, 2023
Mullerian aplasia and hyperandrogenism1Feb 19, 2023
Multicentric osteolysis nodulosis arthropathy spectrum4Mar 5, 2021
Multicentric osteolysis, nodulosis, and arthropathy1Feb 19, 2023
Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome1Feb 21, 2021
Multiple acyl-CoA dehydrogenase deficiency166Dec 7, 2023
Multiple benign circumferential skin creases on limbs 13Oct 2, 2023
Multiple congenital anomalies-hypotonia-seizures syndrome 114Oct 2, 2023
Multiple congenital anomalies-hypotonia-seizures syndrome 24Feb 21, 2021
Multiple congenital anomalies-hypotonia-seizures syndrome 33Mar 5, 2021
Multiple congenital exostosis2Feb 21, 2021
Multiple cutaneous and mucosal venous malformations1Oct 16, 2017
Multiple endocrine neoplasia type 440Dec 7, 2023
Multiple endocrine neoplasia, type 180Dec 7, 2023
Multiple epiphyseal dysplasia type 11Feb 21, 2021
Multiple epiphyseal dysplasia type 42Feb 19, 2023
Multiple epiphyseal dysplasia, Al-Gazali type11Mar 5, 2021
Multiple gastrointestinal atresias6Mar 5, 2021
Multiple mitochondrial dysfunctions syndrome 12Oct 2, 2023
Multiple mitochondrial dysfunctions syndrome 24Feb 21, 2021
Multiple mitochondrial dysfunctions syndrome 32Mar 5, 2021
Multiple mitochondrial dysfunctions syndrome 42Mar 5, 2021
Multiple mitochondrial dysfunctions syndrome 65Mar 5, 2021
Multiple myeloma1Feb 21, 2021
Multiple sclerosis, susceptibility to, 31Mar 5, 2021
Multiple self-healing squamous epithelioma2Oct 2, 2023
Multiple sulfatase deficiency5Mar 12, 2023
Multiple system atrophy1Mar 5, 2021
Multiple system atrophy 1, susceptibility to2Dec 14, 2023
Multisystemic smooth muscle dysfunction syndrome2Feb 19, 2023
Muscle AMP deaminase deficiency3Mar 5, 2021
Muscle eye brain disease3Sep 27, 2019
Muscular dystrophy, limb-girdle, autosomal dominant 4176Dec 7, 2023
Muscular dystrophy, limb-girdle, autosomal recessive 231Feb 21, 2021
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 43Sep 27, 2019
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 74Feb 21, 2021
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A181Dec 14, 2023
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A142Feb 21, 2021
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A245Dec 7, 2023
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A379Dec 7, 2023
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A563Dec 7, 2023
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A64Mar 5, 2021
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A92Feb 21, 2021
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 101Mar 5, 2021
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 113Mar 5, 2021
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 122Mar 5, 2021
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 85Mar 5, 2021
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B12Feb 21, 2021
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B141Feb 21, 2021
Muscular dystrophy-dystroglycanopathy type B61Feb 21, 2021
Myasthenic syndrome, congenital, 222Feb 21, 2021
Myasthenic syndrome, congenital, 24, presynaptic5Feb 21, 2021
Myelodysplastic syndrome2Feb 19, 2023
Myeloproliferative disorder, chronic, with eosinophilia1Mar 5, 2021
Myhre syndrome2Feb 21, 2021
Myoclonic dystonia 115Oct 2, 2023
Myoclonic dystonia 261Feb 21, 2021
Myoclonic-astatic epilepsy3Mar 5, 2021
Myoclonus, familial, 11Mar 5, 2021
Myoclonus, familial, 25Oct 2, 2023
Myoclonus, intractable, neonatal3Mar 5, 2021
Myofibrillar myopathy 102Feb 19, 2023
Myofibrillar myopathy 111Feb 19, 2023
Myofibrillar myopathy 21Mar 5, 2021
Myofibrillar myopathy 31Feb 21, 2021
Myofibrillar myopathy 58Dec 14, 2023
Myofibrillar myopathy 62Feb 21, 2021
Myofibrillar myopathy 72Mar 5, 2021
Myofibrillar myopathy 83Mar 5, 2021
Myofibromatosis, infantile, 22Mar 5, 2021
Myoglobinuria, acute recurrent, autosomal recessive5Oct 2, 2023
Myopathy, centronuclear, 23Mar 5, 2021
Myopathy, centronuclear, 510Feb 19, 2023
Myopathy, congenital, progressive, with scoliosis1Feb 21, 2021
Myopathy, congenital, with respiratory insufficiency and bone fractures1Oct 2, 2023
Myopathy, distal, 52Feb 19, 2023
Myopathy, distal, with rimmed vacuoles2Oct 2, 2023
Myopathy, lactic acidosis, and sideroblastic anemia 119Dec 7, 2023
Myopathy, lactic acidosis, and sideroblastic anemia 23Feb 21, 2021
Myopathy, myofibrillar, 9, with early respiratory failure66Oct 2, 2023
Myopathy, myosin storage, autosomal recessive16Dec 14, 2023
Myopathy, proximal, and ophthalmoplegia6Oct 2, 2023
Myopathy, reducing body, X-linked, childhood-onset1Mar 14, 2019
Myopathy, reducing body, X-linked, early-onset, severe1Mar 14, 2019
Myopathy, tubular aggregate, 11Feb 21, 2021
Myopathy, tubular aggregate, 21Feb 21, 2021
Myopia 21, autosomal dominant1Mar 5, 2021
Myosclerosis3Mar 5, 2021
Myosin storage myopathy22Oct 2, 2023
NAD(P)HX dehydratase deficiency3Feb 21, 2021
NDE1-related microhydranencephaly1Feb 21, 2021
NPHP3-related Meckel-like syndrome4Feb 21, 2021
Nail-patella syndrome1Oct 2, 2023
Nail-patella-like renal disease1Oct 2, 2023
Nance-Horan syndrome2Feb 21, 2021
Nemaline myopathy 105Mar 5, 2021
Nemaline myopathy 244Mar 5, 2021
Nemaline myopathy 53Feb 21, 2021
Nemaline myopathy 62Feb 21, 2021
Nemaline myopathy 71Feb 21, 2021
Nemaline myopathy 86Mar 5, 2021
Nemaline myopathy 91Feb 21, 2021
Neonatal diabetes mellitus with congenital hypothyroidism8Feb 19, 2023
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome5Mar 5, 2021
Neonatal ichthyosis-sclerosing cholangitis syndrome1Apr 1, 2019
Neonatal intrahepatic cholestasis due to citrin deficiency10Oct 2, 2023
Neonatal pseudo-hydrocephalic progeroid syndrome3Mar 12, 2023
Neonatal severe primary hyperparathyroidism1Mar 5, 2021
Neonatal-onset encephalopathy with rigidity and seizures8Mar 5, 2021
Nephrolithiasis, calcium oxalate2Feb 21, 2021
Nephronophthisis 11Apr 1, 2019
Nephronophthisis 128Oct 2, 2023
Nephronophthisis 134Oct 2, 2023
Nephronophthisis 143Feb 21, 2021
Nephronophthisis 153Feb 19, 2023
Nephronophthisis 163Mar 5, 2021
Nephronophthisis 183Oct 2, 2023
Nephronophthisis 206Oct 2, 2023
Nephronophthisis 47Feb 19, 2023
Nephronophthisis 72Mar 5, 2021
Nephronophthisis 91Feb 21, 2021
Nephropathic cystinosis71Dec 7, 2023
Nephrotic syndrome 145Oct 2, 2023
Nephrotic syndrome, IIa 261Oct 2, 2023
Nephrotic syndrome, type 121Feb 19, 2023
Nephrotic syndrome, type 171Feb 21, 2021
Nephrotic syndrome, type 182Feb 21, 2021
Nephrotic syndrome, type 191Feb 21, 2021
Nephrotic syndrome, type 253Dec 7, 2023
Nephrotic syndrome, type 211Feb 19, 2023
Nephrotic syndrome, type 231Oct 2, 2023
Nephrotic syndrome, type 243Oct 2, 2023
Nephrotic syndrome, type 35Mar 5, 2021
Nephrotic syndrome, type 63Oct 2, 2023
Nephrotic syndrome, type 82Feb 21, 2021
Nephrotic syndrome, type 94Oct 2, 2023
Netherton syndrome4Mar 5, 2021
Neu-Laxova syndrome 17Mar 12, 2023
Neural tube defects, folate-sensitive128Feb 23, 2024
Neuroblastoma, susceptibility to, 232Dec 7, 2023
Neuroblastoma, susceptibility to, 3208Dec 7, 2023
Neurodegeneration with ataxia and late-onset optic atrophy1Feb 19, 2023
Neurodegeneration with brain iron accumulation 2B2Mar 5, 2021
Neurodegeneration with brain iron accumulation 55Mar 12, 2023
Neurodegeneration with brain iron accumulation 64Mar 5, 2021
Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures3Feb 21, 2021
Neurodegeneration, childhood-onset, with cerebellar atrophy3Feb 21, 2021
Neurodegeneration, infantile-onset, biotin-responsive1Oct 2, 2023
Neurodevelopmental delay2Feb 23, 2023
Neurodevelopmental disorder2Feb 19, 2023
Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity2Feb 19, 2023
Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter1Feb 21, 2021
Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia1Feb 21, 2021
Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies5Oct 2, 2023
Neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies4Feb 19, 2023
Neurodevelopmental disorder with central and peripheral motor dysfunction5Feb 19, 2023
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction3Oct 2, 2023
Neurodevelopmental disorder with cerebellar atrophy and with or without seizures3Feb 19, 2023
Neurodevelopmental disorder with cerebellar hypoplasia and spasticity1Feb 19, 2023
Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities4Oct 2, 2023
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies14Oct 2, 2023
Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies2Dec 14, 2023
Neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities1Oct 2, 2023
Neurodevelopmental disorder with dystonia and seizures1Oct 2, 2023
Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum1Feb 21, 2021
Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination1Feb 19, 2023
Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities3Feb 19, 2023
Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities2Oct 2, 2023
Neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation1Oct 2, 2023
Neurodevelopmental disorder with hypotonia, neuropathy, and deafness4Feb 19, 2023
Neurodevelopmental disorder with hypotonia, seizures, and absent language11Oct 2, 2023
Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia4Feb 19, 2023
Neurodevelopmental disorder with impaired language and ataxia and with or without seizures2Oct 2, 2023
Neurodevelopmental disorder with impaired speech and hyperkinetic movements11Oct 2, 2023
Neurodevelopmental disorder with involuntary movements3Feb 19, 2023
Neurodevelopmental disorder with language impairment and behavioral abnormalities1Feb 19, 2023
Neurodevelopmental disorder with microcephaly and dysmorphic facies1Feb 19, 2023
Neurodevelopmental disorder with microcephaly and structural brain anomalies1Feb 21, 2021
Neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies5Oct 2, 2023
Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities4Mar 5, 2021
Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity1Feb 21, 2021
Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies4Mar 5, 2021
Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities1Feb 19, 2023
Neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy20Oct 2, 2023
Neurodevelopmental disorder with midbrain and hindbrain malformations1Feb 21, 2021
Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures4Oct 2, 2023
Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart15Oct 2, 2023
Neurodevelopmental disorder with or without autism or seizures2Feb 19, 2023
Neurodevelopmental disorder with or without early-onset generalized epilepsy4Dec 14, 2023
Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive1Feb 21, 2021
Neurodevelopmental disorder with or without seizures and gait abnormalities3Feb 19, 2023
Neurodevelopmental disorder with or without variable brain abnormalities; NEDBA6Dec 14, 2023
Neurodevelopmental disorder with or without variable movement or behavioral abnormalities1Oct 2, 2023
Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies4Mar 5, 2021
Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities2Dec 14, 2023
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures8Feb 21, 2021
Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements2Oct 2, 2023
Neurodevelopmental disorder with severe motor impairment and absent language3Mar 5, 2021
Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies1Feb 21, 2021
Neurodevelopmental disorder with spasticity and poor growth2Mar 5, 2021
Neurodevelopmental disorder with speech impairment and dysmorphic facies2Feb 19, 2023
Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies1Feb 21, 2021
Neurodevelopmental disorder with visual defects and brain anomalies3Feb 19, 2023
Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures7Feb 19, 2023
Neurofibromatosis, type 125Oct 2, 2023
Neurofibromatosis, type 27Dec 6, 2021
Neurogenic scapuloperoneal syndrome, Kaeser type2Feb 19, 2023
Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset1Feb 21, 2021
Neuronal ceroid lipofuscinosis 142Dec 7, 2023
Neuronal ceroid lipofuscinosis 101Mar 5, 2021
Neuronal ceroid lipofuscinosis 29Mar 5, 2021
Neuronal ceroid lipofuscinosis 359Dec 7, 2023
Neuronal ceroid lipofuscinosis 538Dec 7, 2023
Neuronal ceroid lipofuscinosis 71Feb 21, 2021
Neuronal ceroid lipofuscinosis 82Mar 12, 2023
Neuronopathy, distal hereditary motor, autosomal recessive 41Feb 19, 2023
Neuronopathy, distal hereditary motor, type 2A1Feb 21, 2021
Neuronopathy, distal hereditary motor, type 2B1Feb 21, 2021
Neuronopathy, distal hereditary motor, type 2D1Feb 21, 2021
Neuronopathy, distal hereditary motor, type 5A1Feb 19, 2023
Neuronopathy, distal hereditary motor, type 5B4Feb 19, 2023
Neuronopathy, distal hereditary motor, type 7A1Feb 19, 2023
Neuronopathy, distal hereditary motor, type 7B6Oct 2, 2023
Neurooculocardiogenitourinary syndrome2Feb 19, 2023
Neuropathy, hereditary motor and sensory, type 6A5Oct 2, 2023
Neuropathy, hereditary motor and sensory, type 6B1Feb 21, 2021
Neuropathy, hereditary sensory and autonomic, type 2A5Mar 5, 2021
Neuropathy, hereditary sensory and autonomic, type 2B3Mar 5, 2021
Neuropathy, hereditary sensory, type 1D2Mar 5, 2021
Neuropathy, hereditary sensory, type 2C7Dec 14, 2023
Neutral 1 amino acid transport defect1Mar 5, 2021
Neutral lipid storage myopathy2Mar 5, 2021
Neutropenia, severe congenital, 1, autosomal dominant2Feb 21, 2021
Neutropenia, severe congenital, 2, autosomal dominant1Feb 21, 2021
Nicolaides-Baraitser syndrome11Oct 2, 2023
Niemann-Pick disease, type A109Dec 7, 2023
Niemann-Pick disease, type B4Mar 12, 2023
Niemann-Pick disease, type C121Mar 5, 2021
Niemann-Pick disease, type C23Mar 5, 2021
Nijmegen breakage syndrome-like disorder160Dec 7, 2023
Nizon-Isidor syndrome2Feb 19, 2023
Non-acquired combined pituitary hormone deficiency with spine abnormalities1Feb 21, 2021
Non-ketotic hyperglycinemia52Dec 7, 2023
Nonimmune chronic idiopathic neutropenia of adults1Feb 21, 2021
Nonpapillary renal cell carcinoma2Dec 6, 2021
Nonsyndromic congenital nail disorder 11Feb 21, 2021
Nonsyndromic congenital nail disorder 82Mar 14, 2019
Noonan syndrome 124Dec 14, 2023
Noonan syndrome 1015Dec 6, 2021
Noonan syndrome 111Feb 21, 2021
Noonan syndrome 122Oct 2, 2023
Noonan syndrome 22Feb 21, 2021
Noonan syndrome 36Feb 21, 2021
Noonan syndrome 49Dec 14, 2023
Noonan syndrome 54Feb 19, 2023
Noonan syndrome 71Feb 21, 2021
Noonan syndrome 83Feb 19, 2023
Noonan syndrome 93Feb 19, 2023
Noonan syndrome-like disorder with loose anagen hair 14Feb 19, 2023
Norman-Roberts syndrome9Mar 5, 2021
Nystagmus 1, congenital, X-linked1Apr 1, 2019
Nystagmus, congenital, autosomal recessive1Oct 2, 2023
O'Donnell-Luria-Rodan syndrome8Oct 2, 2023
Obesity2Mar 5, 2021
Obesity due to leptin receptor gene deficiency1Feb 21, 2021
Obesity due to prohormone convertase I deficiency1Mar 5, 2021
Obsessive-compulsive disorder1Feb 21, 2021
Occipital pachygyria and polymicrogyria11Mar 5, 2021
Ocular albinism, type II1Mar 5, 2021
Ocular cystinosis2Sep 27, 2019
Oculocerebrofacial syndrome, Kaufman type5Mar 5, 2021
Oculocutaneous albinism type 1B3Feb 21, 2021
Oculocutaneous albinism type 41Nov 14, 2016
Oculodentodigital dysplasia2Feb 21, 2021
Oculofaciocardiodental syndrome4Oct 2, 2023
Oculogastrointestinal-neurodevelopmental syndrome3Feb 19, 2023
Oculomaxillofacial dysostosis1Mar 5, 2021
Oculotrichoanal syndrome1Mar 5, 2021
Ogden syndrome5Feb 21, 2021
Okur-Chung neurodevelopmental syndrome5Mar 5, 2021
Oligodontia-cancer predisposition syndrome10Dec 6, 2021
Olmsted syndrome, X-linked3Oct 2, 2023
Ophthalmoplegia, external, with rib and vertebral anomalies1Feb 21, 2021
Opsismodysplasia3Mar 5, 2021
Optic atrophy 10 with or without ataxia, intellectual disability, and seizures3Oct 2, 2023
Optic atrophy 111Feb 21, 2021
Optic atrophy 31Mar 5, 2021
Optic atrophy 53Mar 14, 2019
Optic atrophy 91Mar 5, 2021
Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy1Mar 5, 2021
Ornithine aminotransferase deficiency51Dec 7, 2023
Ornithine carbamoyltransferase deficiency16Dec 14, 2023
Orofacial-digital syndrome III1Mar 12, 2023
Orofacial-digital syndrome IV2Feb 19, 2023
Orofaciodigital syndrome I4Mar 5, 2021
Orofaciodigital syndrome V1Mar 5, 2021
Orofaciodigital syndrome XV2Mar 5, 2021
Orofaciodigital syndrome type 143Oct 2, 2023
Orofaciodigital syndrome type 64Feb 21, 2021
Orthostatic hypotension 12Oct 2, 2023
Osteochondritis dissecans2Mar 5, 2021
Osteocraniostenosis2Mar 5, 2021
Osteofibrous dysplasia5Dec 6, 2021
Osteogenesis imperfecta12Nov 23, 2018
Osteogenesis imperfecta type 111Feb 21, 2021
Osteogenesis imperfecta type 133Mar 5, 2021
Osteogenesis imperfecta type 141Feb 21, 2021
Osteogenesis imperfecta type 161Mar 5, 2021
Osteogenesis imperfecta type 171Mar 5, 2021
Osteogenesis imperfecta type 61Feb 19, 2023
Osteogenesis imperfecta type 71Feb 21, 2021
Osteogenesis imperfecta type 81Feb 21, 2021
Osteogenesis imperfecta type I12Oct 2, 2023
Osteogenesis imperfecta type III3Feb 21, 2021
Osteogenesis imperfecta with normal sclerae, dominant form5Oct 2, 2023
Osteogenesis imperfecta, perinatal lethal1Mar 14, 2019
Osteogenesis imperfecta, type 181Feb 21, 2021
Osteogenesis imperfecta, type 192Oct 2, 2023
Osteoglophonic dysplasia1Mar 14, 2019
Osteootohepatoenteric syndrome1Feb 19, 2023
Osteopathia striata with cranial sclerosis5Dec 14, 2023
Osteopetrosis with renal tubular acidosis3Feb 19, 2023
Osteoporosis2Oct 2, 2023
Osteoporosis with pseudoglioma3Mar 5, 2021
Oto-palato-digital syndrome, type I2Mar 5, 2021
Otofaciocervical syndrome 23Feb 21, 2021
Otospondylomegaepiphyseal dysplasia, autosomal recessive4Feb 19, 2023
Ovarian dysgenesis 71Feb 21, 2021
Overhydrated hereditary stomatocytosis1Feb 19, 2023
Oxoglutaricaciduria1Feb 21, 2021
PBRM1-related BAFopathy1Jul 1, 2021
PCWH syndrome3Feb 19, 2023
PDS5A-related disorder2Apr 8, 2018
PEHO syndrome1Mar 5, 2021
PEHO-like syndrome1Mar 5, 2021
PERCHING syndrome1Feb 21, 2021
PHARC syndrome2Mar 5, 2021
PHGDH deficiency1Mar 14, 2019
PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome8Feb 19, 2023
PLIN1-related familial partial lipodystrophy2Mar 5, 2021
PLXNA1-related neurodevelopmental disorder1Feb 19, 2023
PMM2-congenital disorder of glycosylation97Dec 7, 2023
PMS1-related breast cancer2Dec 7, 2023
PSAT deficiency2Mar 5, 2021
PULMONARY ALVEOLAR MICROLITHIASIS1Mar 5, 2021
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome4Oct 2, 2023
Pachyonychia congenita 11Mar 5, 2021
Paganini-Miozzo syndrome1Feb 21, 2021
Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome2Feb 21, 2021
Palmoplantar keratoderma, nonepidermolytic, focal 11Feb 21, 2021
Palmoplantar keratoderma, punctate type 1A1Feb 21, 2021
Palmoplantar keratoderma-esophageal carcinoma syndrome87Dec 7, 2023
Pancreatic cancer, susceptibility to, 21Dec 6, 2021
Pancreatic hypoplasia-diabetes-congenital heart disease syndrome2Feb 19, 2023
Pancreatic insufficiency-anemia-hyperostosis syndrome1Mar 5, 2021
Pancytopenia due to IKZF1 mutations1Mar 5, 2021
Pancytopenia-developmental delay syndrome3Mar 5, 2021
Papillary renal cell carcinoma type 13Feb 11, 2022
Papillon-Lefèvre syndrome1Feb 21, 2021
Paragangliomas 232Dec 7, 2023
Paragangliomas 44Feb 10, 2021
Paragangliomas 51Dec 6, 2021
Paramyotonia congenita of Von Eulenburg1Mar 5, 2021
Parenti-mignot neurodevelopmental syndrome2Oct 2, 2023
Parkinson disease 11, autosomal dominant, susceptibility to1Feb 21, 2021
Parkinson disease 18, autosomal dominant, susceptibility to1Feb 21, 2021
Parkinsonism with polyneuropathy1Feb 19, 2023
Parkinsonism-dystonia 3, childhood-onset2Feb 19, 2023
Paroxysmal extreme pain disorder1Oct 2, 2023
Paroxysmal nocturnal hemoglobinuria 11Mar 5, 2021
Partial androgen insensitivity syndrome1Feb 19, 2023
Patent ductus arteriosus 31Mar 5, 2021
Patterned macular dystrophy 256Dec 7, 2023
Pelizaeus-Merzbacher disease8Oct 2, 2023
Pelviscapular dysplasia1Feb 21, 2021
Pendred syndrome14Oct 7, 2022
Periodic fever-infantile enterocolitis-autoinflammatory syndrome1Nov 14, 2016
Peripheral motor neuropathy, childhood-onset, biotin-responsive1Oct 2, 2023
Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development7Feb 19, 2023
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome6Feb 19, 2023
Periventricular heterotopia with microcephaly, autosomal recessive4Mar 5, 2021
Periventricular nodular heterotopia 61Feb 21, 2021
Periventricular nodular heterotopia 74Oct 2, 2023
Periventricular nodular heterotopia 81Feb 19, 2023
Periventricular nodular heterotopia 93Feb 19, 2023
Perlman syndrome32Dec 7, 2023
Permanent neonatal diabetes mellitus 15Feb 19, 2023
Peroxisome biogenesis disorder 10A (Zellweger)1Feb 21, 2021
Peroxisome biogenesis disorder 10B1Feb 21, 2021
Peroxisome biogenesis disorder 12A (Zellweger)3Mar 5, 2021
Peroxisome biogenesis disorder 1A (Zellweger)31Oct 7, 2022
Peroxisome biogenesis disorder 1B29Feb 21, 2021
Peroxisome biogenesis disorder 2A (Zellweger)6Oct 2, 2023
Peroxisome biogenesis disorder 2B4Oct 2, 2023
Peroxisome biogenesis disorder 3A (Zellweger)34Dec 7, 2023
Peroxisome biogenesis disorder 4A (Zellweger)1Mar 14, 2019
Peroxisome biogenesis disorder 4B2Feb 21, 2021
Peroxisome biogenesis disorder 5A (Zellweger)32Dec 7, 2023
Peroxisome biogenesis disorder 6A (Zellweger)45Dec 7, 2023
Peroxisome biogenesis disorder 7A (Zellweger)20Dec 7, 2023
Peroxisome biogenesis disorder 8A (Zellweger)3Mar 12, 2023
Peroxisome biogenesis disorder 8B2Oct 16, 2017
Peroxisome biogenesis disorder 9B38Dec 7, 2023
Perrault syndrome 21Feb 19, 2023
Perrault syndrome 44Feb 19, 2023
Perrault syndrome 51Oct 2, 2023
Perrault syndrome 61Mar 5, 2021
Peters plus syndrome2Oct 2, 2023
Peutz-Jeghers syndrome1Mar 5, 2021
Pfeiffer syndrome2Mar 14, 2019
Phelan-McDermid syndrome11Feb 19, 2023
Phenylketonuria256Dec 7, 2023
Pheochromocytoma64Dec 7, 2023
Phosphoenolpyruvate carboxykinase deficiency, cytosolic1Feb 21, 2021
Phosphoenolpyruvate carboxykinase deficiency, mitochondrial5Mar 12, 2023
Phytanic acid storage disease25Dec 7, 2023
Pidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome3Feb 21, 2021
Piebaldism2Mar 5, 2021
Pierpont syndrome1Feb 19, 2023
Pigmentary pallidal degeneration3Dec 14, 2023
Pigmented nodular adrenocortical disease, primary, 23Mar 5, 2021
Pilarowski-Bjornsson syndrome8Oct 2, 2023
Pili torti-deafness syndrome50Dec 7, 2023
Pilomatrixoma1Feb 10, 2021
Pitt-Hopkins syndrome6Mar 5, 2021
Pitt-Hopkins-like syndrome 29Mar 5, 2021
Pituitary adenoma 5, multiple types184Dec 7, 2023
Pituitary hormone deficiency, combined, 225Dec 7, 2023
Pituitary hormone deficiency, combined, 61Feb 19, 2023
Plasminogen deficiency, type I3Mar 5, 2021
Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease4Mar 12, 2023
Platelet-activating factor acetylhydrolase deficiency1Feb 21, 2021
Platelet-type bleeding disorder 103Feb 19, 2023
Platelet-type bleeding disorder 111Feb 19, 2023
Platelet-type bleeding disorder 152Feb 19, 2023
Platelet-type bleeding disorder 164Feb 19, 2023
Platelet-type bleeding disorder 171Feb 19, 2023
Platelet-type bleeding disorder 204Oct 2, 2023
Poikiloderma with neutropenia3Mar 5, 2021
Poirier-Bienvenu neurodevelopmental syndrome2Feb 19, 2023
Polycystic kidney disease 24Mar 5, 2021
Polycystic kidney disease 3 with or without polycystic liver disease3Oct 2, 2023
Polycystic kidney disease 4369Feb 23, 2024
Polycystic kidney disease 51Feb 21, 2021
Polycystic kidney disease, adult type23Feb 19, 2023
Polycystic liver disease 11Mar 5, 2021
Polydactyly, postaxial, type A11Nov 14, 2016
Polydactyly, postaxial, type A81Mar 5, 2021
Polydactyly, postaxial, type A91Feb 19, 2023
Polydactyly, postaxial, type a71Feb 21, 2021
Polyendocrine-polyneuropathy syndrome2Mar 5, 2021
Polyglandular autoimmune syndrome, type 12Mar 5, 2021
Polyglucosan body myopathy type 11Mar 5, 2021
Polyglucosan body myopathy type 21Feb 19, 2023
Polymicrogyria with optic nerve hypoplasia4Mar 5, 2021
Polymicrogyria with or without vascular-type Ehlers-Danlos syndrome3Feb 19, 2023
Polymicrogyria, bilateral perisylvian, autosomal recessive1Mar 5, 2021
Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis7Feb 19, 2023
Polyposis syndrome, hereditary mixed, 2100Dec 7, 2023
Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal94Dec 7, 2023
Pontocerebellar hypoplasia type 105Mar 5, 2021
Pontocerebellar hypoplasia type 1A4Oct 7, 2022
Pontocerebellar hypoplasia type 1B2Mar 5, 2021
Pontocerebellar hypoplasia type 2A8Oct 2, 2023
Pontocerebellar hypoplasia type 2B3Mar 12, 2023
Pontocerebellar hypoplasia type 2D4Feb 19, 2023
Pontocerebellar hypoplasia type 2E5Mar 5, 2021
Pontocerebellar hypoplasia type 319Mar 5, 2021
Pontocerebellar hypoplasia type 43Feb 21, 2021
Pontocerebellar hypoplasia type 53Mar 5, 2021
Pontocerebellar hypoplasia type 6103Dec 7, 2023
Pontocerebellar hypoplasia type 72Feb 21, 2021
Pontocerebellar hypoplasia type 87Feb 19, 2023
Pontocerebellar hypoplasia type 91Feb 19, 2023
Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal2Feb 19, 2023
Pontocerebellar hypoplasia, type 114Mar 5, 2021
Pontocerebellar hypoplasia, type 1C2Feb 21, 2021
Porencephaly 26Oct 2, 2023
Porokeratosis 8, disseminated superficial actinic type1Mar 5, 2021
Porphobilinogen synthase deficiency1Mar 5, 2021
Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome4Oct 2, 2023
Posterior column ataxia-retinitis pigmentosa syndrome2Mar 5, 2021
Postmenopausal osteoporosis1Feb 21, 2021
Prader-Willi syndrome6Feb 21, 2021
Precocious puberty, central, 21Feb 21, 2021
Predisposition to Wilm's tumor, FBXW7-related1Dec 7, 2023
Predisposition to Wilms tumor, CTR9-related1Dec 7, 2023
Premature chromatid separation trait3Dec 7, 2023
Premature ovarian failure 152Dec 7, 2023
Premature ovarian failure 161Feb 21, 2021
Premature ovarian failure 51Feb 21, 2021
Pretibial dystrophic epidermolysis bullosa2Mar 14, 2019
Primary ciliary dyskinesia 102Feb 19, 2023
Primary ciliary dyskinesia 133Feb 21, 2021
Primary ciliary dyskinesia 143Oct 2, 2023
Primary ciliary dyskinesia 153Mar 5, 2021
Primary ciliary dyskinesia 172Mar 5, 2021
Primary ciliary dyskinesia 186Dec 14, 2023
Primary ciliary dyskinesia 191Feb 21, 2021
Primary ciliary dyskinesia 201Feb 21, 2021
Primary ciliary dyskinesia 211Mar 5, 2021
Primary ciliary dyskinesia 231Oct 2, 2023
Primary ciliary dyskinesia 245Mar 5, 2021
Primary ciliary dyskinesia 273Mar 5, 2021
Primary ciliary dyskinesia 285Mar 5, 2021
Primary ciliary dyskinesia 293Oct 2, 2023
Primary ciliary dyskinesia 314Mar 5, 2021
Primary ciliary dyskinesia 304Mar 5, 2021
Primary ciliary dyskinesia 321Mar 5, 2021
Primary ciliary dyskinesia 331Mar 5, 2021
Primary ciliary dyskinesia 351Mar 5, 2021
Primary ciliary dyskinesia 57Feb 19, 2023
Primary ciliary dyskinesia 720Oct 2, 2023
Primary dilated cardiomyopathy3Feb 19, 2023
Primary erythromelalgia4Oct 2, 2023
Primary hyperoxaluria, type I71Dec 7, 2023
Primary hyperoxaluria, type II41Dec 7, 2023
Primary hypomagnesemia3Feb 19, 2023
Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency4Mar 5, 2021
Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection5Mar 5, 2021
Primary intraosseous venous malformation1Feb 21, 2021
Primary myelofibrosis2Feb 19, 2023
Primrose syndrome5Feb 19, 2023
Progressive demyelinating neuropathy with bilateral striatal necrosis2Oct 2, 2023
Progressive encephalopathy with leukodystrophy due to DECR deficiency1Feb 21, 2021
Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome7Mar 5, 2021
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 12Feb 21, 2021
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 33Oct 2, 2023
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 43Mar 5, 2021
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 13Feb 21, 2021
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 41Feb 19, 2023
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 52Feb 21, 2021
Progressive familial intrahepatic cholestasis type 14Feb 21, 2021
Progressive familial intrahepatic cholestasis type 23Feb 21, 2021
Progressive familial intrahepatic cholestasis type 36Oct 2, 2023
Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome2Feb 21, 2021
Progressive myoclonic epilepsy type 32Feb 21, 2021
Progressive myoclonic epilepsy type 51Aug 17, 2015
Progressive myoclonic epilepsy type 61Feb 19, 2023
Progressive myoclonic epilepsy type 72Feb 21, 2021
Progressive myoclonic epilepsy type 81Feb 21, 2021
Progressive myoclonic epilepsy type 95Mar 5, 2021
Progressive myositis ossificans1Mar 14, 2019
Progressive pseudorheumatoid dysplasia3Feb 19, 2023
Progressive sclerosing poliodystrophy130Dec 7, 2023
Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome2Feb 21, 2021
Prolidase deficiency1Feb 21, 2021
Propionic acidemia158Dec 7, 2023
Prostate cancer, hereditary, 91Dec 7, 2023
Proteasome-associated autoinflammatory syndrome 11Mar 5, 2021
Proteasome-associated autoinflammatory syndrome 31Mar 5, 2021
Protoporphyria, erythropoietic, 12Oct 2, 2023
Proximal 16p11.2 microdeletion syndrome5Apr 1, 2019
Proximal myopathy with extrapyramidal signs3Oct 2, 2023
Pseudo-Hurler polydystrophy1Feb 21, 2021
Pseudo-TORCH syndrome 12Feb 21, 2021
Pseudo-TORCH syndrome 31Dec 14, 2023
Pseudohyperaldosteronism type 21Feb 21, 2021
Pseudohypoaldosteronism type 2C3Mar 5, 2021
Pseudohypoaldosteronism type 2D1Feb 19, 2023
Pseudohypoaldosteronism type 2E2Feb 19, 2023
Pseudohypoparathyroidism2Mar 5, 2021
Pseudohypoparathyroidism type 1B1Apr 1, 2019
Pseudopseudohypoparathyroidism5Dec 14, 2023
Pseudoxanthoma elasticum, forme fruste1Aug 17, 2015
Psychomotor retardation, epilepsy, and craniofacial dysmorphism1Mar 5, 2021
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 11Feb 10, 2021
Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 31Mar 5, 2021
Pulmonary fibrosis and/or bone marrow failure, telomere-related, 51Feb 21, 2021
Pulmonary hypertension, neonatal, susceptibility to94Feb 2, 2024
Pulmonary hypertension, primary, 12Feb 19, 2023
Pulmonary hypertension, primary, 21Feb 21, 2021
Pulmonary venoocclusive disease 13Feb 19, 2023
Purine-nucleoside phosphorylase deficiency3Feb 19, 2023
Pyknodysostosis31Dec 7, 2023
Pyogenic arthritis-pyoderma gangrenosum-acne syndrome1Oct 2, 2023
Pyridoxal phosphate-responsive seizures2Feb 21, 2021
Pyridoxine-dependent epilepsy5Mar 5, 2021
Pyropoikilocytosis, hereditary2Mar 5, 2021
Pyruvate carboxylase deficiency37Dec 14, 2023
Pyruvate dehydrogenase E1-alpha deficiency12Mar 12, 2023
Pyruvate dehydrogenase E1-beta deficiency10Dec 7, 2023
Pyruvate dehydrogenase E2 deficiency3Oct 2, 2023
Pyruvate dehydrogenase E3 deficiency39Dec 14, 2023
Pyruvate dehydrogenase E3-binding protein deficiency6Dec 14, 2023
Pyruvate dehydrogenase phosphatase deficiency1Feb 19, 2023
Pyruvate kinase deficiency of red cells2Mar 5, 2021
Pyruvate kinase hyperactivity1Feb 21, 2021
Quebec platelet disorder1Feb 21, 2021
RAB23-related Carpenter syndrome1Feb 21, 2021
RASopathy48Oct 16, 2017
RFT1-congenital disorder of glycosylation4Oct 2, 2023
RHOB-related disorder1Feb 19, 2023
RIDDLE syndrome4Feb 19, 2023
RYR1-Related Disorders1Apr 6, 2023
Rabson-Mendenhall syndrome1Mar 5, 2021
Radial aplasia-thrombocytopenia syndrome2Feb 21, 2021
Radio-Tartaglia syndrome6Dec 14, 2023
Radioulnar synostosis with amegakaryocytic thrombocytopenia 22Oct 2, 2023
Rafiq syndrome18Oct 2, 2023
Rauch-Steindl syndrome1Oct 2, 2023
Recessive dystrophic epidermolysis bullosa5Mar 12, 2023
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome1Feb 21, 2021
Regressive spondylometaphyseal dysplasia1Feb 21, 2021
Renal carnitine transport defect112Dec 14, 2023
Renal cysts and diabetes syndrome2Oct 2, 2023
Renal hypodysplasia/aplasia 13Mar 5, 2021
Renal hypodysplasia/aplasia 33Feb 19, 2023
Renal tubular acidosis with progressive nerve deafness1Feb 21, 2021
Renal tubular dysgenesis2Feb 21, 2021
Renal-hepatic-pancreatic dysplasia 23Feb 19, 2023
Renpenning syndrome6Mar 5, 2021
Reticular dysgenesis4Mar 5, 2021
Retinal arterial tortuosity1Feb 21, 2021
Retinal dystrophy with or without macular staphyloma2Mar 5, 2021
Retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndrome1Feb 19, 2023
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations2Mar 14, 2019
Retinitis pigmentosa 192Mar 14, 2019
Retinitis pigmentosa 25316Dec 14, 2023
Retinitis pigmentosa 2667Dec 7, 2023
Retinitis pigmentosa 271Mar 12, 2023
Retinitis pigmentosa 2853Dec 7, 2023
Retinitis pigmentosa 33Feb 19, 2023
Retinitis pigmentosa 351Feb 19, 2023
Retinitis pigmentosa 383Feb 19, 2023
Retinitis pigmentosa 39553Mar 14, 2024
Retinitis pigmentosa 441Mar 5, 2021
Retinitis pigmentosa 452Feb 21, 2021
Retinitis pigmentosa 491Feb 19, 2023
Retinitis pigmentosa 5123Dec 7, 2023
Retinitis pigmentosa 599Dec 7, 2023
Retinitis pigmentosa 6130Dec 7, 2023
Retinitis pigmentosa 671Mar 12, 2023
Retinitis pigmentosa 71Feb 21, 2021
Retinitis pigmentosa 701Feb 21, 2021
Retinitis pigmentosa 711Mar 5, 2021
Retinitis pigmentosa 782Mar 5, 2021
Retinitis pigmentosa and erythrocytic microcytosis1Feb 21, 2021
Retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without deafness1Feb 19, 2023
Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome2Feb 19, 2023
Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome1Feb 21, 2021
Retinoblastoma8Oct 2, 2023
Rett syndrome12Dec 14, 2023
Rett syndrome, congenital variant6Oct 2, 2023
Revesz syndrome2Feb 10, 2021
Reynolds syndrome1Feb 21, 2021
Rhabdoid tumor predisposition syndrome 116Dec 7, 2023
Rhabdoid tumor predisposition syndrome 2133Dec 7, 2023
Rhabdomyosarcoma, embryonal, 21Dec 6, 2021
Rheumatoid arthritis1Feb 21, 2021
Rhizomelic chondrodysplasia punctata type 116Sep 27, 2019
Rhizomelic chondrodysplasia punctata type 222Dec 7, 2023
Rhizomelic chondrodysplasia punctata type 316Dec 7, 2023
Rhizomelic chondrodysplasia punctata type 53Oct 2, 2023
Right atrial isomerism2Feb 19, 2023
Ritscher-Schinzel syndrome 12Feb 21, 2021
Ritscher-Schinzel syndrome 25Oct 2, 2023
Ritscher-Schinzel syndrome 42Oct 2, 2023
Roberts-SC phocomelia syndrome2Feb 21, 2021
Robinow-Sorauf syndrome1Mar 5, 2021
Rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked1Feb 19, 2023
Rothmund-Thomson syndrome1Oct 16, 2017
Rothmund-Thomson syndrome type 234Feb 11, 2022
Rotor syndrome5Feb 19, 2023
Rubinstein-Taybi syndrome due to CREBBP mutations17Oct 2, 2023
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency11Mar 5, 2021
SHORT syndrome3Oct 2, 2023
SHOX-related short stature1Nov 14, 2016
SIN3A-related intellectual disability syndrome due to a point mutation6Oct 2, 2023
SKIN/HAIR/EYE PIGMENTATION 1, BLUE/NONBLUE EYES79Dec 7, 2023
SKIN/HAIR/EYE PIGMENTATION 3, LIGHT/DARK SKIN81Dec 7, 2023
SLC35A1-congenital disorder of glycosylation1Feb 21, 2021
SLC35A2-congenital disorder of glycosylation4Oct 2, 2023
SLC39A8-CDG4Feb 21, 2021
SLIT3-related anomalies of the kidney and urinary tract5Oct 2, 2023
SMARCA2-related BAFopathy9Jul 1, 2021
SMARCA4-related BAFopathy11Jul 1, 2021
SMARCB1-related BAFopathy4Jul 1, 2021
SMARCC1-associated developmental dysgenesis syndrome4Jul 1, 2021
SMARCC2-related BAFopathy4Jul 1, 2021
SRD5A3-congenital disorder of glycosylation3Feb 21, 2021
SSR4-congenital disorder of glycosylation2Feb 19, 2023
STAG2-related disorder6Apr 8, 2018
STAT3-related early-onset multisystem autoimmune disease2Mar 5, 2021
STT3A-congenital disorder of glycosylation1Feb 21, 2021
SUDDEN INFANT DEATH SYNDROME1Feb 19, 2023
Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome1Feb 21, 2021
Saldino-Mainzer syndrome3Mar 5, 2021
Salla disease42Dec 7, 2023
Sandhoff disease10Oct 2, 2023
Sarcotubular myopathy2Mar 5, 2021
Scapuloperoneal spinal muscular atrophy1Feb 19, 2023
Schaaf-Yang syndrome13Dec 14, 2023
Schimke immuno-osseous dysplasia2Mar 5, 2021
Schinzel-Giedion syndrome5Oct 2, 2023
Schizencephaly1Dec 14, 2023
Schuurs-Hoeijmakers syndrome2Feb 19, 2023
Schwannomatosis 2210Dec 7, 2023
Schwartz-Jampel syndrome5Feb 21, 2021
Schwartz-Jampel syndrome type 11Feb 19, 2023
Scoliosis, isolated, susceptibility to, 31Mar 5, 2021
Seckel syndrome 11Mar 5, 2021
Seckel syndrome 101Mar 5, 2021
Seckel syndrome 42Mar 5, 2021
Seckel syndrome 52Feb 19, 2023
Seckel syndrome 63Mar 5, 2021
Seckel syndrome 74Mar 5, 2021
Seckel syndrome 82Mar 5, 2021
Seckel syndrome 91Mar 5, 2021
Secondary microcephaly10Jul 10, 2017
See cases3Aug 22, 2022
Seizure8Feb 23, 2023
Seizures, benign familial infantile, 21Oct 2, 2023
Seizures, benign familial infantile, 33Feb 21, 2021
Seizures, benign familial infantile, 59Oct 2, 2023
Seizures, benign familial neonatal, 12Mar 5, 2021
Seizures, benign familial neonatal, 25Mar 5, 2021
Seizures-scoliosis-macrocephaly syndrome1Mar 5, 2021
Sengers syndrome3Mar 5, 2021
Senior-Loken syndrome 41Feb 21, 2021
Senior-Loken syndrome 535Dec 7, 2023
Senior-Loken syndrome 63Mar 5, 2021
Senior-Loken syndrome 82Mar 14, 2019
Senior-Loken syndrome 93Oct 2, 2023
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis2Feb 19, 2023
Septo-optic dysplasia sequence1Feb 21, 2021
Sessile serrated polyposis cancer syndrome101Dec 7, 2023
Severe X-linked mitochondrial encephalomyopathy4Dec 7, 2023
Severe X-linked myotubular myopathy8Dec 7, 2023
Severe achondroplasia-developmental delay-acanthosis nigricans syndrome1Mar 14, 2019
Severe combined immunodeficiency due to CARMIL2 deficiency4Dec 14, 2023
Severe combined immunodeficiency due to CORO1A deficiency1Mar 5, 2021
Severe combined immunodeficiency due to CTPS1 deficiency1Feb 21, 2021
Severe combined immunodeficiency due to DNA-PKcs deficiency14Mar 5, 2021
Severe combined immunodeficiency due to IKK2 deficiency2Mar 5, 2021
Severe combined immunodeficiency due to LAT deficiency2Mar 5, 2021
Severe combined immunodeficiency due to LCK deficiency2Mar 5, 2021
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency70Dec 7, 2023
Severe early-childhood-onset retinal dystrophy5Feb 21, 2021
Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency2Mar 5, 2021
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome11Mar 12, 2023
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome4Oct 2, 2023
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome7Dec 14, 2023
Severe intellectual disability-progressive spastic diplegia syndrome6Feb 19, 2023
Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome5Mar 5, 2021
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome3Feb 21, 2021
Severe myoclonic epilepsy in infancy17Mar 12, 2023
Severe neonatal hypotonia improving with age1Oct 16, 2017
Severe neonatal-onset encephalopathy with microcephaly3Feb 21, 2021
Severe neurodegenerative syndrome with lipodystrophy4Mar 5, 2021
Shashi-Pena syndrome5Mar 5, 2021
Short QT syndrome type 31Mar 14, 2019
Short stature12Jul 17, 2021
Short stature due to growth hormone secretagogue receptor deficiency1Mar 5, 2021
Short stature due to primary acid-labile subunit deficiency3Mar 5, 2021
Short stature with microcephaly and distinctive facies4Feb 21, 2021
Short stature, microcephaly, and endocrine dysfunction1Oct 2, 2023
Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay2Mar 5, 2021
Short stature-brachydactyly-obesity-global developmental delay syndrome4Mar 5, 2021
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome5Mar 5, 2021
Short stature-optic atrophy-Pelger-HuC+t anomaly syndrome4Feb 19, 2023
Short-rib thoracic dysplasia 10 with or without polydactyly2Dec 14, 2023
Short-rib thoracic dysplasia 11 with or without polydactyly1Feb 21, 2021
Short-rib thoracic dysplasia 13 with or without polydactyly2Feb 21, 2021
Short-rib thoracic dysplasia 14 with polydactyly1Feb 21, 2021
Short-rib thoracic dysplasia 19 with or without polydactyly1Feb 21, 2021
Short-rib thoracic dysplasia 6 with or without polydactyly3Feb 19, 2023
Short-rib thoracic dysplasia 7 with or without polydactyly1Feb 21, 2021
Shprintzen-Goldberg syndrome6Mar 12, 2023
Shukla-Vernon syndrome4Oct 2, 2023
Shwachman-Diamond syndrome 16Feb 19, 2023
Shwachman-Diamond syndrome 23Mar 5, 2021
Sialic acid storage disease, severe infantile type2Feb 21, 2021
Sialuria6Feb 21, 2021
Siddiqi syndrome2Feb 19, 2023
Sideroblastic anemia 21Oct 16, 2017
Sideroblastic anemia 32Feb 21, 2021
Sifrim-Hitz-Weiss syndrome12Oct 2, 2023
Silver-Russell syndrome 11Apr 1, 2019
Silver-Russell syndrome 31Feb 19, 2023
Simpson-Golabi-Behmel syndrome type 16Dec 6, 2021
Simpson-Golabi-Behmel syndrome type 24Oct 2, 2023
Singleton-Merten syndrome 12Oct 2, 2023
Sitosterolemia 12Mar 5, 2021
Sitosterolemia 21Feb 21, 2021
Situs inversus2May 29, 2016
Sjögren-Larsson syndrome7Oct 2, 2023
Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome1Oct 2, 2023
Skraban-Deardorff syndrome3Mar 5, 2021
Smith-Lemli-Opitz syndrome50Dec 14, 2023
Smith-Magenis syndrome8Oct 2, 2023
Sneddon syndrome2Mar 5, 2021
Snijders Blok-Campeau syndrome6Oct 2, 2023
Snijders blok-fisher syndrome2Oct 2, 2023
Snowflake vitreoretinal degeneration1Feb 21, 2021
Somatotroph adenoma43Dec 7, 2023
Sotos syndrome21Oct 2, 2023
Southeast Asian ovalocytosis1Oct 2, 2023
Spastic ataxia 25Mar 12, 2023
Spastic ataxia 44Mar 5, 2021
Spastic ataxia 53Mar 5, 2021
Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy3Feb 19, 2023
Spastic paraplegia2Oct 16, 2017
Spastic paraplegia 52, autosomal recessive2Mar 5, 2021
Spastic paraplegia 80, autosomal dominant1Oct 2, 2023
Spastic paraplegia 86, autosomal recessive1Dec 14, 2023
Spastic paraplegia, intellectual disability, nystagmus, and obesity6Mar 5, 2021
Spastic paraplegia, optic atropy, and neuropathy1Feb 21, 2021
Spastic paraplegia-severe developmental delay-epilepsy syndrome1Feb 21, 2021
Spastic tetraplegia and axial hypotonia, progressive1Feb 19, 2023
Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome1Mar 12, 2023
Specific language impairment 51Apr 1, 2019
Spermatogenic failure 111Feb 21, 2021
Spermatogenic failure 171Feb 21, 2021
Spermatogenic failure 182Mar 5, 2021
Spermatogenic failure 191Feb 21, 2021
Spermatogenic failure 201Feb 21, 2021
Spermatogenic failure 231Feb 19, 2023
Spermatogenic failure 251Feb 21, 2021
Spermatogenic failure 2831Mar 12, 2023
Spermatogenic failure 291Feb 21, 2021
Spermatogenic failure 302Feb 21, 2021
Spermatogenic failure 391Feb 19, 2023
Spermatogenic failure 401Feb 21, 2021
Spermatogenic failure 451Feb 19, 2023
Spermatogenic failure 511Feb 19, 2023
Spermatogenic failure 651Feb 19, 2023
Spinal muscular atrophy with congenital bone fractures 22Feb 21, 2021
Spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant1Feb 19, 2023
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome3Mar 5, 2021
Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits1Feb 21, 2021
Spinocerebellar ataxia 442Mar 5, 2021
Spinocerebellar ataxia 451Feb 19, 2023
Spinocerebellar ataxia 473Oct 2, 2023
Spinocerebellar ataxia type 111Feb 21, 2021
Spinocerebellar ataxia type 133Feb 19, 2023
Spinocerebellar ataxia type 142Feb 19, 2023
Spinocerebellar ataxia type 15/166Mar 12, 2023
Spinocerebellar ataxia type 171Mar 5, 2021
Spinocerebellar ataxia type 19/222Dec 14, 2023
Spinocerebellar ataxia type 231Mar 5, 2021
Spinocerebellar ataxia type 253Mar 12, 2023
Spinocerebellar ataxia type 281Feb 21, 2021
Spinocerebellar ataxia type 294Feb 21, 2021
Spinocerebellar ataxia type 341Feb 21, 2021
Spinocerebellar ataxia type 351Mar 5, 2021
Spinocerebellar ataxia type 361Feb 21, 2021
Spinocerebellar ataxia type 405Feb 19, 2023
Spinocerebellar ataxia type 427Mar 5, 2021
Spinocerebellar ataxia type 57Feb 19, 2023
Spinocerebellar ataxia type 66Mar 5, 2021
Spinocerebellar ataxia, autosomal recessive 222Mar 5, 2021
Spinocerebellar ataxia, autosomal recessive 231Feb 21, 2021
Spinocerebellar ataxia, autosomal recessive 261Mar 5, 2021
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 13Mar 5, 2021
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 26Feb 19, 2023
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 31Feb 21, 2021
Split hand-foot malformation 31Apr 1, 2019
Split hand-foot malformation 61Feb 21, 2021
Split-foot malformation-mesoaxial polydactyly syndrome1Feb 21, 2021
Spondylo-megaepiphyseal-metaphyseal dysplasia1Feb 21, 2021
Spondylo-ocular syndrome1Feb 21, 2021
Spondylocostal dysostosis 1, autosomal recessive4Oct 2, 2023
Spondylocostal dysostosis 2, autosomal recessive1Feb 21, 2021
Spondylocostal dysostosis 52Mar 5, 2021
Spondylocostal dysostosis 6, autosomal recessive1Feb 19, 2023
Spondyloenchondrodysplasia with immune dysregulation3Mar 5, 2021
Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures4Oct 2, 2023
Spondyloepimetaphyseal dysplasia with multiple dislocations5Oct 2, 2023
Spondyloepimetaphyseal dysplasia, Bieganski type1Feb 21, 2021
Spondyloepimetaphyseal dysplasia, Isidor-Toutain type1Feb 21, 2021
Spondyloepimetaphyseal dysplasia, PAPSS2 type2Feb 21, 2021
Spondyloepimetaphyseal dysplasia, aggrecan type3Mar 5, 2021
Spondyloepimetaphyseal dysplasia, matrilin-3 type1Feb 21, 2021
Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome4Feb 19, 2023
Spondyloepiphyseal dysplasia with metatarsal shortening1Feb 21, 2021
Spondylometaphyseal dysplasia, Sedaghatian type1Feb 21, 2021
Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome3Mar 5, 2021
Spongy degeneration of central nervous system54Dec 7, 2023
Squalene synthase deficiency2Feb 21, 2021
Stankiewicz-Isidor syndrome2Mar 5, 2021
Steel syndrome4Mar 5, 2021
Sterile multifocal osteomyelitis with periostitis and pustulosis1Feb 21, 2021
Sterol carrier protein 2 deficiency1Mar 5, 2021
Stickler syndrome type 12Oct 2, 2023
Stickler syndrome type 25Feb 19, 2023
Stickler syndrome, type 41Mar 5, 2021
Stiff skin syndrome3Feb 19, 2023
Stormorken syndrome2Oct 2, 2023
Striatonigral degeneration, childhood-onset2Mar 5, 2021
Stromme syndrome15Oct 2, 2023
Structural heart defects and renal anomalies syndrome5Oct 2, 2023
Stuve-Wiedemann syndrome3Feb 21, 2021
Succinate-semialdehyde dehydrogenase deficiency4Feb 19, 2023
Succinyl-CoA acetoacetate transferase deficiency1Feb 21, 2021
Sucrase-isomaltase deficiency3Feb 19, 2023
Sudden infant death-dysgenesis of the testes syndrome1Feb 21, 2021
Suleiman-El-Hattab syndrome1Feb 19, 2023
Sulfite oxidase deficiency1Feb 21, 2021
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A25Dec 7, 2023
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B4Oct 2, 2023
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C4Feb 19, 2023
Surfactant metabolism dysfunction, pulmonary, 11Feb 21, 2021
Surfactant metabolism dysfunction, pulmonary, 22Oct 2, 2023
Surfactant metabolism dysfunction, pulmonary, 52Mar 5, 2021
Susceptibility to respiratory infections associated with CD8alpha chain mutation1Mar 5, 2021
Symmetrical dyschromatosis of extremities1Mar 5, 2021
Syndactyly type 52Oct 2, 2023
Syndromic X-linked intellectual disability 141Feb 21, 2021
Syndromic X-linked intellectual disability 946Dec 14, 2023
Syndromic X-linked intellectual disability Claes-Jensen type10Oct 2, 2023
Syndromic X-linked intellectual disability Lubs type5Oct 2, 2023
Syndromic X-linked intellectual disability Najm type6Oct 2, 2023
Syndromic X-linked intellectual disability Nascimento type1Apr 1, 2019
Syndromic X-linked intellectual disability Raymond type1Feb 21, 2021
Syndromic X-linked intellectual disability Shashi type1Feb 21, 2021
Syndromic X-linked intellectual disability Siderius type8Feb 19, 2023
Syndromic X-linked intellectual disability Snyder type2Oct 2, 2023
Syndromic microphthalmia type 51Oct 16, 2017
Syndromic multisystem autoimmune disease due to ITCH deficiency1Feb 21, 2021
Synpolydactyly type 11Mar 14, 2019
Synpolydactyly type 21Feb 21, 2021
T-B+ severe combined immunodeficiency due to JAK3 deficiency7Mar 5, 2021
T-cell immunodeficiency, congenital alopecia, and nail dystrophy6Dec 14, 2023
T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant1Feb 19, 2023
TARP syndrome4Dec 14, 2023
TCF12-related craniosynostosis4Mar 5, 2021
TELO2-related intellectual disability-neurodevelopmental disorder6Feb 19, 2023
TFRC-related combined immunodeficiency5Mar 5, 2021
THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome10Mar 12, 2023
TMEM165-congenital disorder of glycosylation1Mar 5, 2021
TWIST1-related craniosynostosis1Mar 5, 2021
Tall stature-intellectual disability-renal anomalies syndrome2Dec 14, 2023
Tangier disease4Oct 2, 2023
Tatton-Brown-Rahman overgrowth syndrome1Feb 21, 2021
Tay-Sachs disease9Feb 19, 2023
Tay-Sachs disease, variant AB2Feb 21, 2021
Telangiectasia, hereditary hemorrhagic, type 13Dec 7, 2023
Telangiectasia, hereditary hemorrhagic, type 24Oct 2, 2023
Telangiectasia, hereditary hemorrhagic, type 51Mar 5, 2021
Temple-Baraitser syndrome1Feb 21, 2021
Temtamy syndrome3Mar 5, 2021
Testicular anomalies with or without congenital heart disease7Dec 14, 2023
Tetralogy of Fallot8Oct 2, 2023
Thanatophoric dysplasia type 15Feb 19, 2023
Thanatophoric dysplasia, type 22Mar 14, 2019
Thrombocythemia 13Feb 19, 2023
Thrombocythemia 21Mar 5, 2021
Thrombocythemia 31Mar 5, 2021
Thrombocytopenia 25Dec 7, 2023
Thrombocytopenia 31Mar 5, 2021
Thrombocytopenia 41Mar 5, 2021
Thrombocytopenia 53Mar 5, 2021
Thrombocytopenia 71Dec 14, 2023
Thrombocytopenia, anemia, and myelofibrosis1Feb 21, 2021
Thrombomodulin-related bleeding disorder1Feb 21, 2021
Thrombophilia due to activated protein C resistance2Oct 2, 2023
Thrombophilia due to protein C deficiency, autosomal recessive1Dec 14, 2023
Thrombophilia due to protein S deficiency, autosomal dominant1Mar 5, 2021
Thrombophilia due to thrombin defect1Oct 2, 2023
Thromboxane synthetase deficiency1Mar 5, 2021
Thyroid dyshormonogenesis 62Feb 19, 2023
Thyroid hormone metabolism, abnormal 12Oct 2, 2023
Tibial muscular dystrophy33Oct 2, 2023
Timothy syndrome2Feb 21, 2021
Tooth agenesis, selective, 71Mar 5, 2021
Torsion dystonia 44Feb 19, 2023
Tourette syndrome1Mar 5, 2021
Townes-Brocks syndrome 11Mar 5, 2021
Transcobalamin II deficiency3Feb 19, 2023
Transient bullous dermolysis of the newborn2Mar 14, 2019
Transient infantile hypertriglyceridemia and hepatosteatosis4Feb 19, 2023
Transketolase deficiency4Feb 19, 2023
Transposition of the great arteries, dextro-looped1Mar 5, 2021
Treacher Collins syndrome 21Mar 5, 2021
Treacher Collins syndrome 32Mar 14, 2019
Tremor, hereditary essential, 54Oct 2, 2023
Trichohepatoenteric syndrome 19Feb 21, 2021
Trichohepatoenteric syndrome 21Oct 16, 2017
Trichorhinophalangeal dysplasia type I2Feb 21, 2021
Trichothiodystrophy 1, photosensitive20Feb 19, 2023
Trichothiodystrophy 2, photosensitive7Dec 7, 2023
Trichothiodystrophy 4, nonphotosensitive1Feb 21, 2021
Trichothiodystrophy 5, nonphotosensitive2Feb 21, 2021
Trichotillomania1Feb 21, 2021
Trigonocephaly 11Mar 14, 2019
Trigonocephaly 23Mar 5, 2021
Trimethylaminuria1Feb 19, 2023
Tropical pancreatitis2Dec 7, 2023
Troyer syndrome2Feb 19, 2023
Tuberous sclerosis 19Feb 19, 2023
Tuberous sclerosis 221Dec 6, 2021
Tubulointerstitial kidney disease, autosomal dominant, 21Feb 21, 2021
Tumor predisposition syndrome 31Dec 14, 2023
Tumoral calcinosis, hyperphosphatemic, familial, 12Feb 21, 2021
Type 1 diabetes mellitus 207Dec 6, 2021
Type 2 diabetes mellitus183Dec 7, 2023
Type A2 brachydactyly1Mar 5, 2021
Type II complement component 8 deficiency2Mar 5, 2021
Tyrosinase-negative oculocutaneous albinism5Mar 12, 2023
Tyrosinase-positive oculocutaneous albinism1Feb 21, 2021
Tyrosinemia type I74Dec 7, 2023
Tyrosinemia type II18Dec 7, 2023
UBR5-related diseases1Oct 2, 2023
UDPglucose-4-epimerase deficiency1Feb 21, 2021
Ullrich congenital muscular dystrophy 1A17Feb 19, 2023
Ullrich congenital muscular dystrophy 24Mar 5, 2021
Ulnar-mammary syndrome3Feb 19, 2023
Upshaw-Schulman syndrome6Mar 12, 2023
Urocanate hydratase deficiency1Mar 5, 2021
Urofacial syndrome type 11Feb 21, 2021
Uruguay Faciocardiomusculoskeletal syndrome2Feb 19, 2023
Usher syndrome type 118Oct 7, 2022
Usher syndrome type 1C2Mar 12, 2023
Usher syndrome type 1D2Mar 12, 2023
Usher syndrome type 2A17Mar 12, 2023
Usher syndrome type 2C12Dec 14, 2023
Usher syndrome type 2D1Feb 19, 2023
Usher syndrome type 32Sep 27, 2019
Uveal coloboma-cleft lip and palate-intellectual disability1Mar 5, 2021
VACTERL association1Feb 19, 2023
VACTERL with hydrocephalus1Mar 14, 2019
Van Maldergem syndrome 16Oct 2, 2023
Van Maldergem syndrome 24Feb 19, 2023
Van den Ende-Gupta syndrome3Feb 21, 2021
Van der Woude syndrome 11Oct 16, 2017
Vanishing white matter disease16Oct 2, 2023
Vas deferens, congenital bilateral aplasia of, X-linked1Feb 21, 2021
Vasculitis due to ADA2 deficiency6Feb 19, 2023
Velocardiofacial syndrome2Oct 2, 2023
Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome8Oct 2, 2023
Ventricular septal defect 11Feb 21, 2021
Ventricular septal defect 21Dec 14, 2023
Ventriculomegaly-cystic kidney disease2Feb 21, 2021
Vertebral anomalies and variable endocrine and T-cell dysfunction3Oct 2, 2023
Vertebral, cardiac, renal, and limb defects syndrome 21Dec 14, 2023
Vertebral, cardiac, renal, and limb defects syndrome 31Feb 19, 2023
Ververi-Brady syndrome2Feb 19, 2023
Very long chain acyl-CoA dehydrogenase deficiency174Dec 14, 2023
Vesicoureteral reflux 21Mar 5, 2021
Vesicoureteral reflux 82Mar 5, 2021
Vici syndrome13Mar 5, 2021
Visceral myopathy 13Feb 19, 2023
Vitamin D hydroxylation-deficient rickets, type 1B1Feb 19, 2023
Vitamin D-dependent rickets, type 1A3Oct 2, 2023
Vitelliform macular dystrophy 41Feb 21, 2021
Vitelliform macular dystrophy 51Mar 5, 2021
Von Hippel-Lindau syndrome3Dec 6, 2021
WAPL-related disorder1Apr 8, 2018
WHIM syndrome 11Feb 19, 2023
Waardenburg syndrome type 11Feb 21, 2021
Waardenburg syndrome type 2A1Feb 21, 2021
Waardenburg syndrome type 2E1Nov 14, 2016
Waardenburg syndrome type 31Mar 5, 2021
Warburg micro syndrome 13Feb 21, 2021
Warburg micro syndrome 21Mar 14, 2019
Warburg micro syndrome 41Feb 21, 2021
Warsaw breakage syndrome4Mar 5, 2021
Weaver syndrome1Feb 10, 2021
Webb-Dattani syndrome1Mar 5, 2021
Weill-Marchesani 4 syndrome, recessive1Mar 5, 2021
Weill-Marchesani syndrome 12Mar 5, 2021
Weill-Marchesani syndrome 2, dominant1Mar 5, 2021
Weiss-kruszka syndrome5Feb 19, 2023
Welander distal myopathy1Feb 21, 2021
Werner syndrome121Dec 7, 2023
Wieacker-Wolff syndrome1Oct 2, 2023
Wieacker-Wolff syndrome, female-restricted1Oct 2, 2023
Wiedemann-Steiner syndrome24Oct 2, 2023
Williams syndrome6Feb 19, 2023
Wilms tumor 110Oct 2, 2023
Wilson disease272Dec 7, 2023
Wilson-Turner syndrome2Oct 2, 2023
Wiskott-Aldrich syndrome2Feb 21, 2021
Wiskott-Aldrich syndrome 21Mar 5, 2021
Wolcott-Rallison dysplasia23Dec 7, 2023
Wolfram syndrome 17Oct 2, 2023
Woodhouse-Sakati syndrome3Feb 19, 2023
Woolly hair-skin fragility syndrome2Feb 21, 2021
X-linked Alport syndrome11Oct 2, 2023
X-linked Opitz G/BBB syndrome1Feb 21, 2021
X-linked agammaglobulinemia with growth hormone deficiency1Mar 5, 2021
X-linked central congenital hypothyroidism with late-onset testicular enlargement1Mar 5, 2021
X-linked cerebral-cerebellar-coloboma syndrome syndrome3Oct 16, 2017
X-linked complicated corpus callosum dysgenesis2Feb 21, 2021
X-linked cone-rod dystrophy 17Dec 7, 2023
X-linked distal spinal muscular atrophy type 36Oct 2, 2023
X-linked dominant chondrodysplasia, Chassaing-Lacombe type1Mar 5, 2021
X-linked dystonia-parkinsonism2Oct 2, 2023
X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome1Feb 21, 2021
X-linked hydrocephalus syndrome2Mar 5, 2021
X-linked ichthyosis with steryl-sulfatase deficiency3Apr 1, 2019
X-linked intellectual disability1Feb 19, 2023
X-linked intellectual disability Cabezas type5Oct 2, 2023
X-linked intellectual disability with marfanoid habitus3Feb 21, 2021
X-linked intellectual disability, Cantagrel type15Oct 2, 2023
X-linked intellectual disability, Stocco dos Santos type10Feb 19, 2023
X-linked intellectual disability, van Esch type1Feb 21, 2021
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome1Feb 21, 2021
X-linked intellectual disability-cerebellar hypoplasia syndrome6Oct 2, 2023
X-linked intellectual disability-psychosis-macroorchidism syndrome2Mar 14, 2019
X-linked intellectual disability-short stature-overweight syndrome4Feb 19, 2023
X-linked lissencephaly with abnormal genitalia1Feb 21, 2021
X-linked lymphoproliferative disease due to XIAP deficiency2Feb 21, 2021
X-linked myopathy with excessive autophagy1Mar 5, 2021
X-linked myopathy with postural muscle atrophy1Mar 14, 2019
X-linked progressive cerebellar ataxia6Feb 19, 2023
X-linked reticulate pigmentary disorder1Feb 19, 2023
X-linked scapuloperoneal muscular dystrophy2Mar 5, 2021
X-linked sideroblastic anemia with ataxia1Oct 2, 2023
X-linked spondyloepimetaphyseal dysplasia3Mar 5, 2021
XFE progeroid syndrome1Feb 21, 2021
Xeroderma pigmentosum group A24Dec 7, 2023
Xeroderma pigmentosum, group C67Dec 7, 2023
Xeroderma pigmentosum, group D3Feb 19, 2023
Xeroderma pigmentosum, group E2Dec 6, 2021
Xeroderma pigmentosum, group F1Mar 12, 2023
Yunis-Varon syndrome2Feb 19, 2023
ZTTK syndrome27Oct 2, 2023
Zimmermann-Laband syndrome 12Mar 5, 2021
Zimmermann-laband syndrome 31Feb 21, 2021
Zinc deficiency, transient neonatal1Mar 5, 2021
alpha Thalassemia3Sep 21, 2023
beta Thalassemia5Mar 5, 2021
gamma-Glutamyltransferase deficiency1Feb 21, 2021
not provided135Apr 1, 2019
von Willebrand disease type 15Mar 5, 2021
von Willebrand disease type 25Oct 2, 2023
von Willebrand disease type 31Feb 21, 2021

Testing in GTR

Disease nameNumber of tests
3 beta-Hydroxysteroid dehydrogenase deficiency1 test
3-Methylglutaconic aciduria type 27 tests
3-Methylglutaconic aciduria type 37 tests
3-hydroxy-3-methylglutaryl-CoA synthase deficiency4 tests
3-methylcrotonyl-CoA carboxylase 1 deficiency11 tests
3-methylcrotonyl-CoA carboxylase 2 deficiency9 tests
3-methylglutaconic aciduria type 18 tests
3-methylglutaconic aciduria type 54 tests
46,XX sex reversal 12 tests
46,XY sex reversal 11 test
6-Pyruvoyl-tetrahydrobiopterin synthase deficiency7 tests
AICA-ribosiduria1 test
ALDH18A1-related de Barsy syndrome1 test
ALG1-congenital disorder of glycosylation5 tests
ALG11-congenital disorder of glycosylation3 tests
ALG12-congenital disorder of glycosylation5 tests
ALG2-congenital disorder of glycosylation2 tests
ALG3-congenital disorder of glycosylation5 tests
ALG6-congenital disorder of glycosylation 1C5 tests
ALG8 congenital disorder of glycosylation4 tests
ALG9 congenital disorder of glycosylation5 tests
Abetalipoproteinaemia4 tests
Abnormal chromosome morphology1 test
Acatalasia1 test
Acetyl-CoA acetyltransferase-2 deficiency1 test
Acetyl-CoA: carboxylase deficiency6 tests
Achondrogenesis type II6 tests
Achondrogenesis, type IB3 tests
Achondroplasia2 tests
Achromatopsia 21 test
Achromatopsia 31 test
Achromatopsia 41 test
Acne inversa, familial, 31 test
Acrocephalosyndactyly type I1 test
Acrodysostosis 1 with or without hormone resistance2 tests
Acromicric dysplasia5 tests
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins6 tests
Acute lymphoid leukemia8 tests
Acute myeloid leukemia22 tests
Acute promyelocytic leukemia1 test
Acyl-CoA dehydrogenase 9 deficiency7 tests
Acyl-CoA oxidase deficiency4 tests
Adenine phosphoribosyltransferase deficiency3 tests
Adenylosuccinate lyase deficiency8 tests
Adrenocortical carcinoma, hereditary17 tests
Adrenoleukodystrophy7 tests
Adult hypophosphatasia9 tests
Adult-onset foveomacular vitelliform dystrophy9 tests
Age related macular degeneration 101 test
Age related macular degeneration 27 tests
Agenesis of the corpus callosum with peripheral neuropathy5 tests
Alagille syndrome due to a JAG1 point mutation3 tests
Alcohol sensitivity, acute1 test
Alkaptonuria1 test
Alpha-1-antitrypsin deficiency5 tests
Alpha-methylacyl-CoA racemase deficiency4 tests
Alstrom syndrome1 test
Alveolar capillary dysplasia with pulmonary venous misalignment8 tests
Alzheimer disease2 tests
Alzheimer disease 31 test
Aminoglycoside-induced deafness5 tests
Amish lethal microcephaly1 test
Amyotrophic lateral sclerosis type 11 test
Amyotrophic lateral sclerosis type 123 tests
Amyotrophic lateral sclerosis type 203 tests
Amyotrophic neuralgia3 tests
Anauxetic dysplasia 14 tests
Androgen resistance syndrome4 tests
Anemia, nonspherocytic hemolytic, due to G6PD deficiency4 tests
Angelman syndrome19 tests
Anhaptoglobinemia1 test
Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome2 tests
Aniridia 11 test
Anophthalmia/microphthalmia-esophageal atresia syndrome1 test
Anterior segment dysgenesis 11 test
Anterior segment dysgenesis 31 test
Anterior segment dysgenesis 41 test
Anxiety2 tests
Aplastic anemia5 tests
Arginase deficiency8 tests
Arginine:glycine amidinotransferase deficiency9 tests
Argininosuccinate lyase deficiency8 tests
Arrhythmogenic cardiomyopathy with wooly hair and keratoderma1 test
Arrhythmogenic right ventricular dysplasia 81 test
Arteriohepatic dysplasia4 tests
Aspartate aminotransferase, serum level of, quantitative trait locus 11 test
Aspartylglucosaminuria6 tests
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia4 tests
Ataxia-telangiectasia syndrome12 tests
Ataxia-telangiectasia-like disorder3 tests
Ataxia-telangiectasia-like disorder 13 tests
Atelosteogenesis type II2 tests
Atrophia bulborum hereditaria4 tests
Autism2 tests
Autism spectrum disorder - epilepsy - arthrogryposis syndrome4 tests
Autism, susceptibility to, X-linked 37 tests
Autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome1 test
Autoimmune lymphoproliferative syndrome type 2B1 test
Autoimmune lymphoproliferative syndrome type 43 tests
Autosomal dominant keratitis-ichthyosis-hearing loss syndrome5 tests
Autosomal dominant nonsyndromic hearing loss 101 test
Autosomal dominant nonsyndromic hearing loss 114 tests
Autosomal dominant nonsyndromic hearing loss 3A5 tests
Autosomal dominant nonsyndromic hearing loss 3B1 test
Autosomal dominant nonsyndromic hearing loss 61 test
Autosomal dominant nonsyndromic hearing loss 641 test
Autosomal dominant optic atrophy classic form5 tests
Autosomal dominant osteopetrosis 11 test
Autosomal dominant osteopetrosis 25 tests
Autosomal dominant vitreoretinochoroidopathy5 tests
Autosomal recessive Alport syndrome4 tests
Autosomal recessive DOPA responsive dystonia5 tests
Autosomal recessive ataxia due to ubiquinone deficiency6 tests
Autosomal recessive bestrophinopathy5 tests
Autosomal recessive congenital ichthyosis 15 tests
Autosomal recessive congenital ichthyosis 4A1 test
Autosomal recessive congenital ichthyosis 4B1 test
Autosomal recessive cutis laxa type 2B1 test
Autosomal recessive early-onset Parkinson disease 61 test
Autosomal recessive early-onset Parkinson disease 71 test
Autosomal recessive limb-girdle muscular dystrophy type 2A3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2C3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2D3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2E3 tests
Autosomal recessive limb-girdle muscular dystrophy type 2M4 tests
Autosomal recessive nonsyndromic hearing loss 124 tests
Autosomal recessive nonsyndromic hearing loss 18A5 tests
Autosomal recessive nonsyndromic hearing loss 1A9 tests
Autosomal recessive nonsyndromic hearing loss 1B1 test
Autosomal recessive nonsyndromic hearing loss 233 tests
Autosomal recessive nonsyndromic hearing loss 316 tests
Autosomal recessive nonsyndromic hearing loss 41 test
Autosomal recessive nonsyndromic hearing loss 741 test
Autosomal recessive nonsyndromic hearing loss 972 tests
Autosomal recessive optic atrophy, OPA7 type1 test
Autosomal recessive osteopetrosis 16 tests
Autosomal recessive osteopetrosis 21 test
Autosomal recessive osteopetrosis 44 tests
Autosomal recessive osteopetrosis 51 test
Autosomal recessive osteopetrosis 72 tests
Autosomal recessive polycystic kidney disease7 tests
Avascular necrosis of femoral head, primary, 16 tests
Avellino corneal dystrophy1 test
Axenfeld-Rieger syndrome type 14 tests
Axenfeld-Rieger syndrome type 31 test
B-cell chronic lymphocytic leukemia1 test
B4GALT1-congenital disorder of glycosylation5 tests
Bannayan-Riley-Ruvalcaba syndrome7 tests
Bardet-Biedl syndrome4 tests
Bardet-Biedl syndrome 18 tests
Bardet-Biedl syndrome 106 tests
Bardet-Biedl syndrome 123 tests
Bardet-Biedl syndrome 145 tests
Bardet-Biedl syndrome 153 tests
Bardet-Biedl syndrome 27 tests
Bardet-Biedl syndrome 33 tests
Bardet-Biedl syndrome 43 tests
Bardet-Biedl syndrome 53 tests
Bardet-Biedl syndrome 73 tests
Bardet-Biedl syndrome 93 tests
Basal cell carcinoma, susceptibility to, 13 tests
Basal cell carcinoma, susceptibility to, 712 tests
Becker muscular dystrophy8 tests
Beckwith-Wiedemann syndrome5 tests
Benign recurrent intrahepatic cholestasis type 15 tests
Benign recurrent intrahepatic cholestasis type 26 tests
Beta-D-mannosidosis1 test
Beta-hydroxyisobutyryl-CoA deacylase deficiency1 test
Bietti crystalline corneoretinal dystrophy1 test
Bifunctional peroxisomal enzyme deficiency7 tests
Biotinidase deficiency12 tests
Birt-Hogg-Dube syndrome5 tests
Blepharophimosis, ptosis, and epicanthus inversus syndrome1 test
Bloom syndrome11 tests
Body mass index quantitative trait locus 122 tests
Body mass index quantitative trait locus 41 test
Bone fragility with contractures, arterial rupture, and deafness1 test
Bone marrow transplant1 test
Bone mineral density quantitative trait locus 11 test
Bone osteosarcoma18 tests
Bothnia retinal dystrophy6 tests
Bradyopsia1 test
Branchiootic syndrome 11 test
Branchiootorenal syndrome 11 test
Breast-ovarian cancer, familial, susceptibility to, 110 tests
Breast-ovarian cancer, familial, susceptibility to, 211 tests
Breast-ovarian cancer, familial, susceptibility to, 34 tests
Breast-ovarian cancer, familial, susceptibility to, 44 tests
Bronchiectasis with or without elevated sweat chloride 16 tests
Bruck syndrome 22 tests
Brunner syndrome1 test
Budd-Chiari syndrome2 tests
Burkitt lymphoma1 test
CBL-related disorder5 tests
CHARGE association7 tests
COACH syndrome 13 tests
COG1 congenital disorder of glycosylation5 tests
COG4-congenital disorder of glycosylation1 test
COG5-congenital disorder of glycosylation3 tests
COG6-ongenital disorder of glycosylation1 test
COG7 congenital disorder of glycosylation5 tests
COG8-congenital disorder of glycosylation5 tests
COVID-191 test
Camptodactyly, tall stature, and hearing loss syndrome (CATSHL syndrome)1 test
Camptodactyly-tall stature-scoliosis-hearing loss syndrome1 test
Carcinoid tumor of intestine4 tests
Carcinoma of colon13 tests
Carcinoma of pancreas17 tests
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 16 tests
Cardiofaciocutaneous syndrome 14 tests
Cardiofaciocutaneous syndrome 31 test
Cardiofaciocutaneous syndrome 41 test
Cardiomyopathy-hypotonia-lactic acidosis syndrome1 test
Carney complex, type 15 tests
Carney-Stratakis syndrome5 tests
Carnitine acylcarnitine translocase deficiency8 tests
Carnitine palmitoyl transferase 1A deficiency12 tests
Carnitine palmitoyl transferase II deficiency, myopathic form11 tests
Carnitine palmitoyl transferase II deficiency, neonatal form11 tests
Carnitine palmitoyl transferase II deficiency, severe infantile form13 tests
Carotid intimal medial thickness 11 test
Cataract 11 multiple types4 tests
Cataract 14 multiple types1 test
Cataract 16 multiple types1 test
Cataract 181 test
Cataract 401 test
Cerebral amyloid angiopathy, APP-related1 test
Ceroid lipofuscinosis, neuronal, 6A5 tests
Cervical cancer1 test
Charcot-Marie-Tooth disease dominant intermediate D1 test
Charcot-Marie-Tooth disease recessive intermediate B6 tests
Charcot-Marie-Tooth disease recessive intermediate D3 tests
Charcot-Marie-Tooth disease type 1B1 test
Charcot-Marie-Tooth disease type 2A11 test
Charcot-Marie-Tooth disease type 2A23 tests
Charcot-Marie-Tooth disease type 2D1 test
Charcot-Marie-Tooth disease type 2I1 test
Charcot-Marie-Tooth disease type 2J1 test
Charcot-Marie-Tooth disease type 4K1 test
Charcot-Marie-Tooth disease, axonal, type 2EE1 test
Charcot-Marie-Tooth disease, type IA1 test
Charlevoix-Saguenay spastic ataxia5 tests
Childhood hypophosphatasia7 tests
Childhood onset GLUT1 deficiency syndrome 23 tests
Cholestanol storage disease6 tests
Cholestasis, intrahepatic, of pregnancy, 11 test
Cholestasis, intrahepatic, of pregnancy, 34 tests
Chondrocalcinosis 21 test
Choroid plexus papilloma17 tests
Choroidal dystrophy, central areolar 26 tests
Choroideremia1 test
Christianson syndrome1 test
Chromosome 8, partial trisomy1 test
Chromosome Xp11.22 duplication syndrome6 tests
Chronic myelogenous leukemia, BCR-ABL1 positive4 tests
Chuvash polycythemia13 tests
Citrullinemia type I9 tests
Citrullinemia type II10 tests
Classic homocystinuria11 tests
Cleidocranial dysostosis3 tests
Cobalamin C disease12 tests
Coenzyme Q10 deficiency, primary, 16 tests
Coenzyme Q10 deficiency, primary, 36 tests
Coloboma of optic nerve2 tests
Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome1 test
Colorectal cancer, hereditary nonpolyposis, type 26 tests
Combined PSAP deficiency1 test
Combined deficiency of sialidase AND beta galactosidase2 tests
Combined immunodeficiency, X-linked3 tests
Combined malonic and methylmalonic acidemia6 tests
Combined molybdoflavoprotein enzyme deficiency9 tests
Combined oxidative phosphorylation defect type 145 tests
Combined oxidative phosphorylation defect type 152 tests
Combined oxidative phosphorylation defect type 21 test
Combined oxidative phosphorylation defect type 245 tests
Combined oxidative phosphorylation defect type 254 tests
Combined oxidative phosphorylation defect type 41 test
Combined oxidative phosphorylation defect type 75 tests
Combined oxidative phosphorylation defect type 86 tests
Combined oxidative phosphorylation defect type 94 tests
Combined oxidative phosphorylation deficiency 224 tests
Combined oxidative phosphorylation deficiency 353 tests
Combined oxidative phosphorylation deficiency 392 tests
Complex cortical dysplasia with other brain malformations 11 test
Conduction disorder of the heart1 test
Cone dystrophy 31 test
Cone dystrophy 41 test
Cone dystrophy with supernormal rod response1 test
Cone monochromatism1 test
Cone-rod dystrophy 13 tests
Cone-rod dystrophy 101 test
Cone-rod dystrophy 126 tests
Cone-rod dystrophy 137 tests
Cone-rod dystrophy 156 tests
Cone-rod dystrophy 161 test
Cone-rod dystrophy 27 tests
Cone-rod dystrophy 37 tests
Cone-rod dystrophy 51 test
Cone-rod dystrophy 66 tests
Cone-rod dystrophy 71 test
Cone-rod dystrophy 91 test
Cone-rod synaptic disorder, congenital nonprogressive7 tests
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency1 test
Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency1 test
Congenital amegakaryocytic thrombocytopenia5 tests
Congenital bilateral aplasia of vas deferens from CFTR mutation6 tests
Congenital bile acid synthesis defect 23 tests
Congenital bile acid synthesis defect 41 test
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome4 tests
Congenital central hypoventilation7 tests
Congenital chromosomal disease2 tests
Congenital diarrhea 5 with tufting enteropathy4 tests
Congenital disorder of deglycosylation3 tests
Congenital disorder of glycosylation type 1E2 tests
Congenital disorder of glycosylation type Ir4 tests
Congenital fibrosis of extraocular muscles type 11 test
Congenital generalized lipodystrophy type 41 test
Congenital hyperammonemia, type I7 tests
Congenital hypomyelinating neuropathy1 test
Congenital hypothyroidism3 tests
Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome1 test
Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type9 tests
Congenital lipoid adrenal hyperplasia due to STAR deficency1 test
Congenital muscular hypertrophy-cerebral syndrome1 test
Congenital myasthenic syndrome 103 tests
Congenital myasthenic syndrome 113 tests
Congenital myasthenic syndrome 131 test
Congenital myasthenic syndrome 4A3 tests
Congenital myasthenic syndrome 4B2 tests
Congenital myasthenic syndrome 4C2 tests
Congenital prothrombin deficiency2 tests
Congenital stationary night blindness 1A1 test
Congenital stationary night blindness 1B1 test
Congenital stationary night blindness 1C1 test
Congenital stationary night blindness 1D1 test
Congenital stationary night blindness 2A1 test
Congenital stationary night blindness autosomal dominant 11 test
Congenital stationary night blindness autosomal dominant 25 tests
Congenital stationary night blindness autosomal dominant 31 test
Corneal dystrophy, Fuchs endothelial, 61 test
Corneal dystrophy, Meesmann, 11 test
Corneal dystrophy, lattice type 3A1 test
Cornelia de Lange syndrome 11 test
Cornelia de Lange syndrome 31 test
Cornelia de Lange syndrome 41 test
Cornelia de Lange syndrome 51 test
Coronary artery disease, autosomal dominant, 12 tests
Corpus callosum agenesis-abnormal genitalia syndrome6 tests
Corticosterone 18-monooxygenase deficiency1 test
Corticosterone methyloxidase type 2 deficiency1 test
Costello syndrome4 tests
Cowden syndrome1 test
Cowden syndrome 114 tests
Craniodiaphyseal dysplasia, autosomal dominant1 test
Craniofacial anomalies and anterior segment dysgenesis syndrome1 test
Craniometaphyseal dysplasia, autosomal dominant1 test
Creatine transporter deficiency6 tests
Crigler-Najjar syndrome2 tests
Crigler-Najjar syndrome type 13 tests
Crigler-Najjar syndrome, type II2 tests
Crouzon syndrome1 test
Crouzon syndrome-acanthosis nigricans syndrome2 tests
Cutis laxa with osteodystrophy2 tests
Cutis laxa, X-linked5 tests
Cutis laxa, autosomal dominant 11 test
Cutis laxa, autosomal dominant 21 test
Cutis laxa, autosomal recessive, type 1A1 test
Cystic fibrosis20 tests
Cystinuria1 test
D-2-hydroxyglutaric aciduria 11 test
D-2-hydroxyglutaric aciduria 21 test
D-Glyceric aciduria1 test
DK1-congenital disorder of glycosylation5 tests
DPAGT1-congenital disorder of glycosylation1 test
DPM3-congenital disorder of glycosylation2 tests
Deafness dystonia syndrome6 tests
Deafness, congenital heart defects, and posterior embryotoxon4 tests
Deafness-encephaloneuropathy-obesity-valvulopathy syndrome1 test
Deafness-lymphedema-leukemia syndrome4 tests
Deficiency of 2-methylbutyryl-CoA dehydrogenase8 tests
Deficiency of 3-hydroxyacyl-CoA dehydrogenase2 tests
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase11 tests
Deficiency of acetyl-CoA acetyltransferase8 tests
Deficiency of alpha-mannosidase6 tests
Deficiency of butyryl-CoA dehydrogenase8 tests
Deficiency of cytochrome-b5 reductase1 test
Deficiency of galactokinase6 tests
Deficiency of guanidinoacetate methyltransferase9 tests
Deficiency of hydroxymethylglutaryl-CoA lyase11 tests
Deficiency of isobutyryl-CoA dehydrogenase6 tests
Deficiency of malonyl-CoA decarboxylase1 test
Deficiency of phosphoserine phosphatase1 test
Deficiency of steroid 11-beta-monooxygenase4 tests
Deficiency of steroid 17-alpha-monooxygenase6 tests
Dejerine-Sottas disease1 test
Dent disease type 24 tests
Dermatofibrosis lenticularis disseminata6 tests
Desmoid disease, hereditary6 tests
Deuteranomaly1 test
Developmental and epileptic encephalopathy, 16 tests
Developmental and epileptic encephalopathy, 27 tests
Developmental and epileptic encephalopathy, 391 test
Developmental and epileptic encephalopathy, 44 tests
Developmental and epileptic encephalopathy, 93 tests
DiGeorge syndrome4 tests
Diabetes mellitus type 11 test
Diamond-Blackfan anemia7 tests
Diamond-Blackfan anemia 51 test
Diaphyseal dysplasia6 tests
Dihydropteridine reductase deficiency2 tests
Dihydropyrimidine dehydrogenase deficiency5 tests
Dilated cardiomyopathy 1GG6 tests
Dilated cardiomyopathy 1J1 test
Dilated cardiomyopathy 1U1 test
Dilated cardiomyopathy 1X1 test
Dilated cardiomyopathy 3B4 tests
Dimethylglycine dehydrogenase deficiency1 test
Dominant beta-thalassemia2 tests
Dopa-responsive dystonia due to sepiapterin reductase deficiency1 test
Doyne honeycomb retinal dystrophy1 test
Drash syndrome3 tests
Duchenne muscular dystrophy10 tests
Dyskeratosis congenita, autosomal recessive 54 tests
Dystonia 161 test
Early myoclonic encephalopathy1 test
Ectodermal dysplasia and immunodeficiency 12 tests
Ectopia lentis 1, isolated, autosomal dominant5 tests
Ehlers-Danlos syndrome progeroid type7 tests
Ehlers-Danlos syndrome type 7A1 test
Ehlers-Danlos syndrome type 7B1 test
Ehlers-Danlos syndrome, arthrochalasia type7 tests
Ehlers-Danlos syndrome, cardiac valvular type7 tests
Ehlers-Danlos syndrome, classic type10 tests
Ehlers-Danlos syndrome, dermatosparaxis type4 tests
Ehlers-Danlos syndrome, kyphoscoliotic type 13 tests
Ehlers-Danlos syndrome, spondylocheirodysplastic type7 tests
Ehlers-Danlos syndrome, type 35 tests
Ehlers-Danlos syndrome, type 47 tests
Ehlers-danlos syndrome, arthrochalasia type, 21 test
Encephalopathy due to GLUT1 deficiency3 tests
Encephalopathy, acute, infection-induced, susceptibility to, 46 tests
Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 14 tests
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome1 test
Endometrial carcinoma16 tests
Enhanced S-cone syndrome2 tests
Epidermal nevus1 test
Epidermolysis bullosa simplex 1A, generalized severe1 test
Epidermolysis bullosa simplex 1C, localized1 test
Epidermolysis bullosa simplex with migratory circinate erythema1 test
Epidermolysis bullosa simplex with mottled pigmentation1 test
Epidermolysis bullosa simplex, Koebner type1 test
Epithelial basement membrane dystrophy1 test
Epsilon-trimethyllysine hydroxylase deficiency6 tests
Ethylmalonic encephalopathy9 tests
Exercise-induced hyperinsulinism3 tests
Exudative vitreoretinopathy 14 tests
Exudative vitreoretinopathy 2, X-linked1 test
Exudative vitreoretinopathy 44 tests
Exudative vitreoretinopathy 54 tests
Fabry disease6 tests
Factor V deficiency2 tests
Familial Mediterranean fever1 test
Familial adenomatous polyposis 112 tests
Familial adenomatous polyposis 27 tests
Familial aplasia of the vermis1 test
Familial atrial myxoma2 tests
Familial cancer of breast37 tests
Familial colorectal cancer5 tests
Familial dysautonomia10 tests
Familial expansile osteolysis2 tests
Familial gestational hyperthyroidism2 tests
Familial hemophagocytic lymphohistiocytosis 22 tests
Familial hypercholesterolemia7 tests
Familial hyperthyroidism due to mutations in TSH receptor2 tests
Familial infantile myasthenia4 tests
Familial isolated deficiency of vitamin E5 tests
Familial medullary thyroid carcinoma4 tests
Familial meningioma9 tests
Familial porphyria cutanea tarda1 test
Familial prostate carcinoma1 test
Familial spontaneous pneumothorax2 tests
Familial steroid-resistant nephrotic syndrome with sensorineural deafness1 test
Fanconi anemia complementation group C9 tests
Fanconi anemia complementation group D110 tests
Fanconi anemia complementation group N8 tests
Fanconi anemia complementation group O1 test
Fanconi renotubular syndrome 27 tests
Fasting plasma glucose level quantitative trait locus 51 test
Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 36 tests
Febrile seizures, familial, 44 tests
Fetal hemoglobin quantitative trait locus 12 tests
Fibromatosis, gingival, 13 tests
Fibrosis of extraocular muscles, congenital, 21 test
Fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement1 test
Finnish congenital nephrotic syndrome5 tests
Focal dermal hypoplasia3 tests
Follicular lymphoma, susceptibility to, 12 tests
Fragile X syndrome9 tests
Fragile X-associated tremor/ataxia syndrome3 tests
Frasier syndrome3 tests
Friedreich ataxia 14 tests
Frontotemporal dementia1 test
Frontotemporal dementia and/or amyotrophic lateral sclerosis 61 test
Fructose-biphosphatase deficiency7 tests
Fumarase deficiency3 tests
GM1 gangliosidosis type 23 tests
GM1 gangliosidosis type 33 tests
GNE myopathy10 tests
GRACILE syndrome7 tests
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions1 test
Galactosylceramide beta-galactosidase deficiency7 tests
Gamma-aminobutyric acid transaminase deficiency1 test
Gastric lymphoma2 tests
Gastrointestinal stromal tumor5 tests
Gaucher disease due to saposin C deficiency1 test
Gaucher disease perinatal lethal6 tests
Gaucher disease type I9 tests
Gaucher disease type II6 tests
Gaucher disease type III6 tests
Geleophysic dysplasia 25 tests
Generalized juvenile polyposis/juvenile polyposis coli9 tests
Glaucoma 1, open angle, A4 tests
Glaucoma 3A7 tests
Glaucoma, normal tension, susceptibility to5 tests
Glioma susceptibility 114 tests
Glioma susceptibility 27 tests
Glioma susceptibility 310 tests
Glucocorticoid-remediable aldosteronism4 tests
Glucose-6-phosphate transport defect9 tests
Glutaric aciduria, type 111 tests
Glutaryl-CoA oxidase deficiency6 tests
Gluthathione peroxidase deficiency1 test
Glycine N-methyltransferase deficiency3 tests
Glycogen storage disease IIIa3 tests
Glycogen storage disease IIIb3 tests
Glycogen storage disease IXa16 tests
Glycogen storage disease IXb6 tests
Glycogen storage disease IXc6 tests
Glycogen storage disease IXd6 tests
Glycogen storage disease XV3 tests
Glycogen storage disease due to glucose-6-phosphatase deficiency type IA11 tests
Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency1 test
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency4 tests
Glycogen storage disease due to muscle and heart glycogen synthase deficiency6 tests
Glycogen storage disease due to muscle beta-enolase deficiency6 tests
Glycogen storage disease type III6 tests
Glycogen storage disease type X6 tests
Glycogen storage disease, type II9 tests
Glycogen storage disease, type IV6 tests
Glycogen storage disease, type V6 tests
Glycogen storage disease, type VI6 tests
Glycogen storage disease, type VII6 tests
Glycogen storage disorder due to hepatic glycogen synthase deficiency7 tests
Gorlin syndrome6 tests
Granulomatous disease, chronic, X-linked1 test
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative1 test
Groenouw corneal dystrophy type I1 test
HNSHA due to aldolase A deficiency1 test
HSD10 mitochondrial disease6 tests
Hawkinsinuria4 tests
Hb SS disease8 tests
Heimler syndrome 11 test
Heimler syndrome 21 test
Heinz body anemia2 tests
Helicoid peripapillary chorioretinal degeneration1 test
Hematologic neoplasm1 test
Hemochromatosis type 14 tests
Hemochromatosis type 2A3 tests
Hemochromatosis type 2B3 tests
Hemochromatosis type 33 tests
Hemochromatosis type 43 tests
Hemolytic anemia due to adenylate kinase deficiency1 test
Hemolytic anemia due to glucophosphate isomerase deficiency1 test
Hemolytic anemia due to hexokinase deficiency1 test
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency1 test
Hepatic adenomas, familial1 test
Hepatic methionine adenosyltransferase deficiency1 test
Hepatocellular carcinoma19 tests
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 18 tests
Hereditary coproporphyria1 test
Hereditary diffuse gastric adenocarcinoma8 tests
Hereditary disease172 tests
Hereditary fructosuria10 tests
Hereditary hemorrhagic telangiectasia2 tests
Hereditary intrinsic factor deficiency6 tests
Hereditary leiomyomatosis and renal cell cancer5 tests
Hereditary liability to pressure palsies1 test
Hereditary motor and sensory neuropathy with optic atrophy2 tests
Hereditary myopathy with lactic acidosis due to ISCU deficiency6 tests
Hereditary pancreatitis6 tests
Hereditary spastic paraplegia 131 test
Hereditary spastic paraplegia 25 tests
Hereditary spastic paraplegia 311 test
Hereditary spastic paraplegia 443 tests
Hereditary spastic paraplegia 551 test
Hereditary spastic paraplegia 74 tests
Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX14 tests
Hereditary xanthinuria type 13 tests
Hermansky-Pudlak syndrome 14 tests
Hermansky-Pudlak syndrome 21 test
Hermansky-Pudlak syndrome 37 tests
Hermansky-Pudlak syndrome 44 tests
Hermansky-Pudlak syndrome 54 tests
Hermansky-Pudlak syndrome 64 tests
Hermansky-Pudlak syndrome 74 tests
Hermansky-Pudlak syndrome 84 tests
Hidrotic ectodermal dysplasia syndrome1 test
Hirschsprung disease, susceptibility to, 14 tests
Holocarboxylase synthetase deficiency8 tests
Holoprosencephaly 31 test
Holoprosencephaly 73 tests
Homocystinuria due to methylene tetrahydrofolate reductase deficiency8 tests
Homocystinuria, cblD type, variant 14 tests
Huntington disease2 tests
Hurler syndrome6 tests
Hurthle cell carcinoma of thyroid5 tests
Hydroxyacyl glutathione hydrolase deficiency1 test
Hyper-IgE recurrent infection syndrome 1, autosomal dominant1 test
Hyper-IgM syndrome type 51 test
Hyperammonemia, type III7 tests
Hypercalcemia, infantile, 11 test
Hyperinsulinemic hypoglycemia, familial, 14 tests
Hyperinsulinemic hypoglycemia, familial, 41 test
Hyperinsulinism due to glucokinase deficiency1 test
Hyperinsulinism-hyperammonemia syndrome4 tests
Hyperlysinemia1 test
Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase3 tests
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome10 tests
Hyperparathyroidism 13 tests
Hyperparathyroidism 2 with jaw tumors4 tests
Hyperphosphatasemia tarda1 test
Hyperphosphatasemia with bone disease2 tests
Hyperprolinemia type 26 tests
Hypertriglyceridemia 11 test
Hypertrophic cardiomyopathy 17 tests
Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome1 test
Hypochondroplasia2 tests
Hypogonadotropic hypogonadism 5 with or without anosmia6 tests
Hypogonadotropic hypogonadism 7 with or without anosmia6 tests
Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome2 tests
Hypomyelinating leukodystrophy 23 tests
Hypomyelinating leukodystrophy 41 test
Hypophosphatemic nephrolithiasis/osteoporosis 16 tests
Hypophosphatemic nephrolithiasis/osteoporosis 22 tests
Hypopigmentation, organomegaly, and delayed myelination and development1 test
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration1 test
Hypospadias 1, X-linked4 tests
Hypothyroidism due to TSH receptor mutations2 tests
Hypotonia with lactic acidemia and hyperammonemia6 tests
IMAGe syndrome2 tests
Ichthyosis, hystrix-like, with hearing loss5 tests
Idiopathic generalized epilepsy1 test
Idiopathic hypereosinophilic syndrome1 test
Imerslund-Grasbeck syndrome1 test
Iminoglycinuria1 test
Immunodeficiency 181 test
Immunodeficiency 233 tests
Immunodeficiency 27A1 test
Immunodeficiency 31B1 test
Immunodeficiency 332 tests
Immunodeficiency 83, susceptibility to viral infections1 test
Inborn glycerol kinase deficiency2 tests
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 11 test
Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 23 tests
Incontinentia pigmenti syndrome5 tests
Increased analgesia from kappa-opioid receptor agonist, female-specific1 test
Infantile GM1 gangliosidosis3 tests
Infantile cerebellar-retinal degeneration1 test
Infantile cortical hyperostosis3 tests
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency4 tests
Infantile hypophosphatasia7 tests
Infantile nephronophthisis3 tests
Infantile neuroaxonal dystrophy2 tests
Infantile onset spinocerebellar ataxia8 tests
Insulin-resistant diabetes mellitus AND acanthosis nigricans2 tests
Intellectual disability, X-linked 631 test
Intellectual disability, X-linked, with or without seizures, arx-related6 tests
Intellectual disability, autosomal dominant 51 test
Intellectual disability, autosomal recessive 75 tests
Iodotyrosine deiodination defect3 tests
Irido-corneo-trabecular dysgenesis1 test
Ischemic stroke8 tests
Isolated microphthalmia 31 test
Isolated microphthalmia 56 tests
Isolated optic nerve hypoplasia1 test
Isovaleryl-CoA dehydrogenase deficiency11 tests
Jackson-Weiss syndrome1 test
Joubert syndrome 27 tests
Joubert syndrome 321 test
Joubert syndrome 56 tests
Joubert syndrome 61 test
Joubert syndrome 91 test
Joubert syndrome with renal defect2 tests
Junctional epidermolysis bullosa gravis of Herlitz4 tests
Junctional epidermolysis bullosa, non-Herlitz type7 tests
Juvenile myelomonocytic leukemia6 tests
Juvenile nephropathic cystinosis3 tests
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome5 tests
Juvenile retinoschisis4 tests
Kahrizi syndrome4 tests
Kennedy disease4 tests
Keratoconus 14 tests
Keratosis palmoplantaris striata 21 test
Kniest dysplasia6 tests
Knuckle pads, deafness AND leukonychia syndrome5 tests
Kostmann syndrome1 test
Krabbe disease due to saposin A deficiency1 test
Kugelberg-Welander disease1 test
L-2-hydroxyglutaric aciduria1 test
LEOPARD syndrome 16 tests
LEOPARD syndrome 25 tests
LEOPARD syndrome 33 tests
Langer-Giedion syndrome1 test
Langereis blood group1 test
Late-onset retinal degeneration1 test
Lattice corneal dystrophy Type I1 test
Leber congenital amaurosis 16 tests
Leber congenital amaurosis 106 tests
Leber congenital amaurosis 117 tests
Leber congenital amaurosis 122 tests
Leber congenital amaurosis 137 tests
Leber congenital amaurosis 147 tests
Leber congenital amaurosis 151 test
Leber congenital amaurosis 162 tests
Leber congenital amaurosis 27 tests
Leber congenital amaurosis 32 tests
Leber congenital amaurosis 42 tests
Leber congenital amaurosis 57 tests
Leber congenital amaurosis 66 tests
Leber congenital amaurosis 76 tests
Leber congenital amaurosis 86 tests
Leber congenital amaurosis 91 test
Legg-Calve-Perthes disease6 tests
Leigh syndrome49 tests
Leprechaunism syndrome1 test
Lesch-Nyhan syndrome6 tests
Lethal acantholytic epidermolysis bullosa1 test
Lethal osteosclerotic bone dysplasia6 tests
Leukemia, acute lymphoblastic, susceptibility to, 35 tests
Leukemia, chronic lymphocytic, susceptibility to, 11 test
Leukocyte adhesion deficiency type II5 tests
Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome6 tests
Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome3 tests
Levy-Hollister syndrome1 test
Lewy body dementia1 test
Li-Fraumeni syndrome 117 tests
Li-Fraumeni syndrome 23 tests
Linear skin defects with multiple congenital anomalies 11 test
Lipoic acid synthetase deficiency1 test
Lissencephaly due to TUBA1A mutation1 test
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency15 tests
Low phospholipid associated cholelithiasis5 tests
Lowe syndrome5 tests
Lung carcinoma12 tests
Lymphatic malformation 33 tests
Lynch syndrome 125 tests
Lynch syndrome 46 tests
Lynch syndrome 56 tests
Lynch syndrome 85 tests
Lysinuric protein intolerance6 tests
Lysosomal acid lipase deficiency4 tests
MASS syndrome5 tests
MGAT2-congenital disorder of glycosylation2 tests
MHC class I deficiency1 test
MOGS-congenital disorder of glycosylation4 tests
MORM syndrome1 test
MPDU1-congenital disorder of glycosylation5 tests
MPI-congenital disorder of glycosylation10 tests
MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA7 tests
MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB4 tests
Macrocephaly-autism syndrome13 tests
Macroglobulinemia, Waldenstrom, 11 test
Macular degeneration, X-linked atrophic4 tests
Macular degeneration, age-related, 31 test
Malignant tumor of esophagus2 tests
Malignant tumor of prostate18 tests
Malignant tumor of testis7 tests
Malignant tumor of urinary bladder5 tests
Maple syrup urine disease12 tests
Maple syrup urine disease type 1A4 tests
Maple syrup urine disease type 1B4 tests
Maple syrup urine disease type 24 tests
Marfan syndrome7 tests
Mastocytosis1 test
Matthew-Wood syndrome1 test
Maturity-onset diabetes of the young type 21 test
Maturity-onset diabetes of the young type 31 test
Maturity-onset diabetes of the young type 61 test
McKusick-Kaufman syndrome3 tests
Meacham syndrome3 tests
Meckel syndrome, type 13 tests
Meckel syndrome, type 31 test
Meckel syndrome, type 46 tests
Meckel syndrome, type 61 test
Medium-chain acyl-coenzyme A dehydrogenase deficiency12 tests
Medulloblastoma14 tests
Megalencephalic leukoencephalopathy with subcortical cysts 15 tests
Melanoma and neural system tumor syndrome4 tests
Melanoma, cutaneous malignant, susceptibility to, 114 tests
Melanoma, cutaneous malignant, susceptibility to, 25 tests
Melanoma, cutaneous malignant, susceptibility to, 37 tests
Melanoma, cutaneous malignant, susceptibility to, 51 test
Melanoma-pancreatic cancer syndrome6 tests
Melorheostosis5 tests
Menkes kinky-hair syndrome6 tests
Meretoja syndrome1 test
Mesothelioma, malignant3 tests
Metabolic myopathy due to lactate transporter defect2 tests
Metachondromatosis5 tests
Metachromatic leukodystrophy6 tests
Metaphyseal chondrodysplasia, McKusick type5 tests
Metaphyseal chondrodysplasia, Schmid type3 tests
Metaphyseal dysplasia without hypotrichosis3 tests
Methemoglobinemia type 41 test
Methylcobalamin deficiency type cblE8 tests
Methylcobalamin deficiency type cblG8 tests
Methylmalonate semialdehyde dehydrogenase deficiency1 test
Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency6 tests
Methylmalonic acidemia due to transcobalamin receptor defect5 tests
Methylmalonic acidemia with homocystinuria, type cblX3 tests
Methylmalonic aciduria and homocystinuria type cblD9 tests
Methylmalonic aciduria and homocystinuria type cblF9 tests
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency15 tests
Methylmalonic aciduria, cblA type11 tests
Methylmalonic aciduria, cblB type11 tests
Microcephalic osteodysplastic dysplasia, Saul-Wilson type2 tests
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability3 tests
Microcephaly, normal intelligence and immunodeficiency10 tests
Microphthalmia, isolated, with coloboma 51 test
Microphthalmia, isolated, with coloboma 71 test
Microvascular complications of diabetes, susceptibility to, 61 test
Microvascular complications of diabetes, susceptibility to, 71 test
Miller syndrome1 test
Mismatch repair cancer syndrome 16 tests
Mitochondrial DNA depletion syndrome 18 tests
Mitochondrial DNA depletion syndrome 112 tests
Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant1 test
Mitochondrial DNA depletion syndrome 133 tests
Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)7 tests
Mitochondrial DNA depletion syndrome 4b9 tests
Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)6 tests
Mitochondrial DNA depletion syndrome 8a8 tests
Mitochondrial DNA depletion syndrome 911 tests
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria7 tests
Mitochondrial DNA depletion syndrome, myopathic form7 tests
Mitochondrial complex 1 deficiency, nuclear type 101 test
Mitochondrial complex 1 deficiency, nuclear type 111 test
Mitochondrial complex 1 deficiency, nuclear type 121 test
Mitochondrial complex 1 deficiency, nuclear type 141 test
Mitochondrial complex 1 deficiency, nuclear type 181 test
Mitochondrial complex 1 deficiency, nuclear type 191 test
Mitochondrial complex 1 deficiency, nuclear type 21 test
Mitochondrial complex 1 deficiency, nuclear type 211 test
Mitochondrial complex 1 deficiency, nuclear type 271 test
Mitochondrial complex 1 deficiency, nuclear type 323 tests
Mitochondrial complex 1 deficiency, nuclear type 41 test
Mitochondrial complex 1 deficiency, nuclear type 51 test
Mitochondrial complex 1 deficiency, nuclear type 73 tests
Mitochondrial complex 1 deficiency, nuclear type 82 tests
Mitochondrial complex 1 deficiency, nuclear type 92 tests
Mitochondrial complex 5 (ATP synthase) deficiency nuclear type 51 test
Mitochondrial complex I deficiency43 tests
Mitochondrial complex I deficiency, nuclear type 12 tests
Mitochondrial complex II deficiency, nuclear type 112 tests
Mitochondrial complex III deficiency nuclear type 19 tests
Mitochondrial complex III deficiency nuclear type 21 test
Mitochondrial complex III deficiency nuclear type 53 tests
Mitochondrial complex IV deficiency, nuclear type 116 tests
Mitochondrial complex V (ATP synthase) deficiency nuclear type 26 tests
Mitochondrial complex V (ATP synthase) deficiency nuclear type 36 tests
Mitochondrial complex V (ATP synthase) deficiency, nuclear type 15 tests
Mitochondrial disease2 tests
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency4 tests
Mitochondrial trifunctional protein deficiency17 tests
Monocytopenia with susceptibility to infections2 tests
Mucolipidosis type II3 tests
Mucolipidosis type IV9 tests
Mucopolysaccharidosis type 71 test
Mucopolysaccharidosis, MPS-I-H/S5 tests
Mucopolysaccharidosis, MPS-I-S5 tests
Mucopolysaccharidosis, MPS-II9 tests
Mucopolysaccharidosis, MPS-III-A6 tests
Mucopolysaccharidosis, MPS-III-B1 test
Mucopolysaccharidosis, MPS-III-C1 test
Mucopolysaccharidosis, MPS-III-D1 test
Mucopolysaccharidosis, MPS-IV-A4 tests
Mucopolysaccharidosis, MPS-IV-B1 test
Muenke syndrome2 tests
Muir-Torré syndrome6 tests
Multiple acyl-CoA dehydrogenase deficiency22 tests
Multiple endocrine neoplasia, type 17 tests
Multiple epiphyseal dysplasia, Beighton type6 tests
Multiple mitochondrial dysfunctions syndrome 11 test
Multiple mitochondrial dysfunctions syndrome 21 test
Multiple myeloma3 tests
Multiple sulfatase deficiency4 tests
Muscle eye brain disease3 tests
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 44 tests
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B44 tests
Mutilating keratoderma5 tests
Myelodysplastic syndrome6 tests
Myelodysplastic syndrome associated with isolated del(5q)1 test
Myhre syndrome4 tests
Myofibrillar myopathy 21 test
Myoglobinuria, acute recurrent, autosomal recessive7 tests
Myopathy, lactic acidosis, and sideroblastic anemia 16 tests
Myopathy, lactic acidosis, and sideroblastic anemia 26 tests
NPHP3-related Meckel-like syndrome1 test
Nail-patella syndrome7 tests
Namaqualand hip dysplasia6 tests
Nance-Horan syndrome1 test
Nanophthalmos 25 tests
Nasopharyngeal carcinoma17 tests
Nemaline myopathy 24 tests
Neonatal intrahepatic cholestasis due to citrin deficiency8 tests
Neoplasm of ovary4 tests
Neoplasm of stomach9 tests
Nephronophthisis 15 tests
Nephronophthisis 112 tests
Nephronophthisis 34 tests
Nephronophthisis 44 tests
Nephronophthisis-like nephropathy 11 test
Nephropathic cystinosis6 tests
Nephrotic syndrome, type 25 tests
Nephrotic syndrome, type 43 tests
Neural tube defects, folate-sensitive13 tests
Neuroblastoma1 test
Neuroblastoma, susceptibility to, 25 tests
Neuroblastoma, susceptibility to, 37 tests
Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities1 test
Neurofibromatosis, type 11 test
Neurofibromatosis, type 26 tests
Neuronal ceroid lipofuscinosis 15 tests
Neuronal ceroid lipofuscinosis 101 test
Neuronal ceroid lipofuscinosis 26 tests
Neuronal ceroid lipofuscinosis 36 tests
Neuronal ceroid lipofuscinosis 55 tests
Neuronal ceroid lipofuscinosis 83 tests
Neuronal ceroid lipofuscinosis 8 northern epilepsy variant2 tests
Neuronopathy, distal hereditary motor, type 5A1 test
Neuropathy, hereditary sensory and autonomic, type 1C1 test
Neurophysiologic defect in schizophrenia5 tests
Neutral 1 amino acid transport defect1 test
Neutral lipid storage myopathy1 test
Newfoundland cone-rod dystrophy5 tests
Niemann-Pick disease, type A10 tests
Niemann-Pick disease, type B1 test
Niemann-Pick disease, type C16 tests
Niemann-Pick disease, type C23 tests
Nijmegen breakage syndrome-like disorder5 tests
Non-Hodgkin lymphoma5 tests
Non-ketotic hyperglycinemia10 tests
Nonpapillary renal cell carcinoma13 tests
Noonan syndrome 17 tests
Noonan syndrome 31 test
Noonan syndrome 44 tests
Noonan syndrome 55 tests
Noonan syndrome 64 tests
Noonan syndrome 73 tests
Noonan syndrome 84 tests
Noonan syndrome 91 test
Noonan syndrome-like disorder with loose anagen hair4 tests
Nystagmus 1, congenital, X-linked1 test
Nystagmus 6, congenital, X-linked7 tests
Obesity3 tests
Obesity due to congenital leptin deficiency2 tests
Obesity due to leptin receptor gene deficiency2 tests
Obesity due to pro-opiomelanocortin deficiency2 tests
Obesity due to prohormone convertase I deficiency2 tests
Obsessive-compulsive disorder2 tests
Occult macular dystrophy1 test
Ocular albinism with congenital sensorineural hearing loss4 tests
Ocular albinism, type I6 tests
Ocular albinism, type II1 test
Ocular cystinosis3 tests
Oculocutaneous albinism type 14 tests
Oculocutaneous albinism type 1B4 tests
Oculocutaneous albinism type 34 tests
Oculocutaneous albinism type 44 tests
Oculofaciocardiodental syndrome1 test
Odontohypophosphatasia4 tests
Oguchi disease5 tests
Oguchi disease-21 test
Opioid dependence, susceptibility to, 11 test
Optic atrophy 37 tests
Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy6 tests
Ornithine aminotransferase deficiency4 tests
Ornithine carbamoyltransferase deficiency8 tests
Orthostatic hypotension 11 test
Osteofibrous dysplasia2 tests
Osteogenesis imperfecta type 116 tests
Osteogenesis imperfecta type 122 tests
Osteogenesis imperfecta type 2, thin-bone1 test
Osteogenesis imperfecta type 54 tests
Osteogenesis imperfecta type 62 tests
Osteogenesis imperfecta type 78 tests
Osteogenesis imperfecta type 82 tests
Osteogenesis imperfecta type 92 tests
Osteogenesis imperfecta type I7 tests
Osteogenesis imperfecta type III6 tests
Osteogenesis imperfecta with normal sclerae, dominant form6 tests
Osteogenesis imperfecta, perinatal lethal6 tests
Osteogenesis imperfecta, type III/IV1 test
Osteopathia striata with cranial sclerosis6 tests
Osteopetrosis with renal tubular acidosis6 tests
Osteoporosis with pseudoglioma1 test
Otofaciocervical syndrome 11 test
Otospondylomegaepiphyseal dysplasia, autosomal recessive6 tests
Oxoglutaricaciduria1 test
PGM1-congenital disorder of glycosylation6 tests
PHARC syndrome6 tests
PHGDH deficiency5 tests
PMM2-congenital disorder of glycosylation12 tests
PPARG-related familial partial lipodystrophy1 test
PYCR1-related de Barsy syndrome1 test
Paget disease of bone 2, early-onset2 tests
Palmoplantar keratoderma-deafness syndrome5 tests
Pancreatic cancer, susceptibility to, 210 tests
Pancreatic cancer, susceptibility to, 38 tests
Pancreatic cancer, susceptibility to, 49 tests
Pancreatic insufficiency-anemia-hyperostosis syndrome1 test
Panic disorder 11 test
Papillary renal cell carcinoma type 15 tests
Papillary thyroid carcinoma1 test
Paragangliomas 14 tests
Paragangliomas 25 tests
Paragangliomas 37 tests
Paragangliomas 48 tests
Paragangliomas 57 tests
Parathyroid carcinoma2 tests
Parkinson disease 13, autosomal dominant, susceptibility to1 test
Paroxysmal nonkinesigenic dyskinesia1 test
Partial androgen insensitivity syndrome4 tests
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency4 tests
Partington syndrome6 tests
Patterned macular dystrophy 15 tests
Pelizaeus-Merzbacher disease6 tests
Pendred syndrome6 tests
Permanent neonatal diabetes mellitus1 test
Peroxisome biogenesis disorder 10A (Zellweger)3 tests
Peroxisome biogenesis disorder 11A (Zellweger)5 tests
Peroxisome biogenesis disorder 12A (Zellweger)3 tests
Peroxisome biogenesis disorder 13A (Zellweger)1 test
Peroxisome biogenesis disorder 14B3 tests
Peroxisome biogenesis disorder 1A (Zellweger)5 tests
Peroxisome biogenesis disorder 2A (Zellweger)3 tests
Peroxisome biogenesis disorder 3A (Zellweger)2 tests
Peroxisome biogenesis disorder 4A (Zellweger)2 tests
Peroxisome biogenesis disorder 5A (Zellweger)5 tests
Peroxisome biogenesis disorder 5B2 tests
Peroxisome biogenesis disorder 6A (Zellweger)3 tests
Peroxisome biogenesis disorder 7A (Zellweger)3 tests
Peroxisome biogenesis disorder 8A (Zellweger)1 test
Peroxisome biogenesis disorder 8B2 tests
Peroxisome biogenesis disorder 9B4 tests
Peroxisome biogenesis disorder type 3B1 test
Perrault syndrome 11 test
Perrault syndrome 25 tests
Peutz-Jeghers syndrome9 tests
Pfeiffer syndrome1 test
Phenylketonuria11 tests
Pheochromocytoma22 tests
Phosphate transport defect5 tests
Phosphoenolpyruvate carboxykinase deficiency, cytosolic3 tests
Phosphoenolpyruvate carboxykinase deficiency, mitochondrial4 tests
Phytanic acid storage disease4 tests
Pick disease1 test
Pigmentary pallidal degeneration1 test
Pigmentary retinal dystrophy9 tests
Pigmented nodular adrenocortical disease, primary, 12 tests
Pigmented paravenous retinochoroidal atrophy6 tests
Pili torti-deafness syndrome5 tests
Pilomatrixoma7 tests
Pituitary hormone deficiency, combined, 25 tests
Pituitary hormone deficiency, combined, 62 tests
Platyspondylic dysplasia, Torrance type6 tests
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 11 test
Polycystic liver disease 3 with or without kidney cysts1 test
Polyglandular autoimmune syndrome, type 13 tests
Polyposis syndrome, hereditary mixed, 24 tests
Pontocerebellar hypoplasia type 66 tests
Posterior column ataxia-retinitis pigmentosa syndrome1 test
Posterior polymorphous corneal dystrophy 11 test
Posterior polymorphous corneal dystrophy 31 test
Postmenopausal osteoporosis8 tests
Prader-Willi syndrome1 test
Pregnancy loss, recurrent, susceptibility to, 12 tests
Pregnancy loss, recurrent, susceptibility to, 22 tests
Premature ovarian failure 13 tests
Premature ovarian failure 31 test
Primary ciliary dyskinesia 141 test
Primary hyperoxaluria, type I6 tests
Primary hyperoxaluria, type II5 tests
Primary open angle glaucoma2 tests
Progressive demyelinating neuropathy with bilateral striatal necrosis1 test
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 17 tests
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 27 tests
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 37 tests
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 48 tests
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 57 tests
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 110 tests
Progressive familial intrahepatic cholestasis5 tests
Progressive familial intrahepatic cholestasis type 11 test
Progressive familial intrahepatic cholestasis type 25 tests
Progressive familial intrahepatic cholestasis type 36 tests
Progressive sclerosing poliodystrophy10 tests
Proline dehydrogenase deficiency1 test
Propionic acidemia21 tests
Protan defect1 test
Protoporphyria, erythropoietic, 11 test
Pseudo-Hurler polydystrophy1 test
Purine-nucleoside phosphorylase deficiency4 tests
Pyknodysostosis9 tests
Pyridoxine-dependent epilepsy5 tests
Pyruvate carboxylase deficiency11 tests
Pyruvate dehydrogenase E1-alpha deficiency5 tests
Pyruvate dehydrogenase E1-beta deficiency6 tests
Pyruvate dehydrogenase E2 deficiency7 tests
Pyruvate dehydrogenase E3 deficiency9 tests
Pyruvate dehydrogenase E3-binding protein deficiency6 tests
Pyruvate dehydrogenase complex deficiency6 tests
Pyruvate dehydrogenase phosphatase deficiency7 tests
RFT1-congenital disorder of glycosylation2 tests
Reis-Bucklers' corneal dystrophy1 test
Renal carnitine transport defect10 tests
Renal coloboma syndrome1 test
Renal cysts and diabetes syndrome1 test
Renal dysplasia and retinal aplasia1 test
Renal-hepatic-pancreatic dysplasia 11 test
Reticular dysgenesis1 test
Reticulate acropigmentation of Kitamura1 test
Retinal cone dystrophy 41 test
Retinal degeneration, autosomal recessive, clumped pigment type4 tests
Retinal macular dystrophy type 25 tests
Retinitis pigmentosa2 tests
Retinitis pigmentosa 11 test
Retinitis pigmentosa 106 tests
Retinitis pigmentosa 116 tests
Retinitis pigmentosa 127 tests
Retinitis pigmentosa 131 test
Retinitis pigmentosa 142 tests
Retinitis pigmentosa 176 tests
Retinitis pigmentosa 197 tests
Retinitis pigmentosa 26 tests
Retinitis pigmentosa 205 tests
Retinitis pigmentosa 256 tests
Retinitis pigmentosa 261 test
Retinitis pigmentosa 275 tests
Retinitis pigmentosa 286 tests
Retinitis pigmentosa 35 tests
Retinitis pigmentosa 306 tests
Retinitis pigmentosa 316 tests
Retinitis pigmentosa 331 test
Retinitis pigmentosa 361 test
Retinitis pigmentosa 373 tests
Retinitis pigmentosa 386 tests
Retinitis pigmentosa 394 tests
Retinitis pigmentosa 41 test
Retinitis pigmentosa 406 tests
Retinitis pigmentosa 415 tests
Retinitis pigmentosa 421 test
Retinitis pigmentosa 431 test
Retinitis pigmentosa 446 tests
Retinitis pigmentosa 456 tests
Retinitis pigmentosa 461 test
Retinitis pigmentosa 476 tests
Retinitis pigmentosa 485 tests
Retinitis pigmentosa 491 test
Retinitis pigmentosa 505 tests
Retinitis pigmentosa 511 test
Retinitis pigmentosa 546 tests
Retinitis pigmentosa 551 test
Retinitis pigmentosa 566 tests
Retinitis pigmentosa 571 test
Retinitis pigmentosa 581 test
Retinitis pigmentosa 5910 tests
Retinitis pigmentosa 601 test
Retinitis pigmentosa 614 tests
Retinitis pigmentosa 76 tests
Retinitis pigmentosa 7, digenic4 tests
Retinitis pigmentosa 91 test
Retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without deafness4 tests
Retinitis punctata albescens4 tests
Retinoblastoma1 test
Rett syndrome8 tests
Rett syndrome, congenital variant3 tests
Rheumatoid arthritis1 test
Rhizomelic chondrodysplasia punctata type 12 tests
Rhizomelic chondrodysplasia punctata type 23 tests
Rhizomelic chondrodysplasia punctata type 34 tests
Ring dermoid of cornea1 test
Rothmund-Thomson syndrome3 tests
Roussy-Lévy syndrome1 test
Rubinstein-Taybi syndrome6 tests
SKIN/HAIR/EYE PIGMENTATION 1, BLUE/NONBLUE EYES6 tests
SKIN/HAIR/EYE PIGMENTATION 3, LIGHT/DARK SKIN4 tests
SLC35A1-congenital disorder of glycosylation5 tests
SLC35A2-congenital disorder of glycosylation3 tests
SRD5A3-congenital disorder of glycosylation2 tests
Saccharopinuria1 test
Salla disease5 tests
Sandhoff disease5 tests
Sarcosine dehydrogenase deficiency1 test
Sarcotubular myopathy1 test
Schaaf-Yang syndrome3 tests
Schizencephaly1 test
Schizophrenia3 tests
Schizophrenia 41 test
Schwannomatosis 13 tests
Sclerosteosis 11 test
Scoliosis, isolated, susceptibility to, 36 tests
Seizures, benign familial neonatal, 13 tests
Sengers syndrome1 test
Senior-Loken syndrome 41 test
Senior-Loken syndrome 57 tests
Senior-Loken syndrome 66 tests
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis9 tests
Septo-optic dysplasia sequence1 test
Severe X-linked mitochondrial encephalomyopathy4 tests
Severe combined immunodeficiency due to DCLRE1C deficiency6 tests
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency8 tests
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive6 tests
Severe early-childhood-onset retinal dystrophy7 tests
Severe neonatal-onset encephalopathy with microcephaly7 tests
Sex-linked hereditary disorder1 test
Shprintzen-Goldberg syndrome5 tests
Shwachman-Diamond syndrome 15 tests
Sialuria2 tests
Sideroblastic anemia 21 test
Simpson-Golabi-Behmel syndrome type 15 tests
Sjögren-Larsson syndrome6 tests
Skin/hair/eye pigmentation, variation in, 114 tests
Skin/hair/eye pigmentation, variation in, 21 test
Skin/hair/eye pigmentation, variation in, 54 tests
Small cell lung carcinoma1 test
Smith-Lemli-Opitz syndrome8 tests
Smith-Magenis syndrome3 tests
Snowflake vitreoretinal degeneration2 tests
Solid tumor2 tests
Solitary median maxillary central incisor syndrome1 test
Sorsby fundus dystrophy1 test
Sotos syndrome1 test
Spastic ataxia 31 test
Spastic ataxia 41 test
Spastic ataxia 51 test
Sphingolipid activator protein 1 deficiency1 test
Spinal muscular atrophy, type II1 test
Spinal muscular atrophy, type IV1 test
Spinocerebellar ataxia type 11 test
Spinocerebellar ataxia type 101 test
Spinocerebellar ataxia type 146 tests
Spinocerebellar ataxia type 281 test
Spondyloepiphyseal dysplasia congenita6 tests
Spondyloepiphyseal dysplasia with metatarsal shortening6 tests
Spondylometaphyseal dysplasia1 test
Spondyloperipheral dysplasia1 test
Spongy degeneration of central nervous system9 tests
Squamous cell carcinoma of the head and neck13 tests
Stargardt disease 31 test
Stargardt disease 45 tests
Steinert myotonic dystrophy syndrome2 tests
Sterol carrier protein 2 deficiency4 tests
Stickler syndrome type 11 test
Stiff skin syndrome5 tests
Succinate-semialdehyde dehydrogenase deficiency7 tests
Succinyl-CoA acetoacetate transferase deficiency1 test
Sulfite oxidase deficiency2 tests
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A1 test
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B5 tests
Supravalvar aortic stenosis1 test
Syndactyly-telecanthus-anogenital and renal malformations syndrome1 test
Syndromic X-linked intellectual disability Lubs type8 tests
Syndromic microphthalmia type 52 tests
Synovial sarcoma1 test
T-B+ severe combined immunodeficiency due to JAK3 deficiency3 tests
TMEM165-congenital disorder of glycosylation3 tests
Tay-Sachs disease13 tests
Tay-Sachs disease, variant AB1 test
Telangiectasia, hereditary hemorrhagic, type 13 tests
Tetralogy of Fallot5 tests
Thanatophoric dysplasia type 12 tests
Thanatophoric dysplasia, type 22 tests
Thiel-Behnke corneal dystrophy1 test
Thrombocythemia 23 tests
Thrombocytopenia 21 test
Thrombocytopenia 41 test
Thrombophilia4 tests
Thrombophilia due to activated protein C resistance2 tests
Thrombophilia due to protein C deficiency, autosomal dominant6 tests
Thrombophilia due to protein C deficiency, autosomal recessive6 tests
Thyroid cancer, nonmedullary, 29 tests
Thyroid hormone metabolism, abnormal 11 test
Transcobalamin II deficiency9 tests
Transferrin serum level quantitative trait locus 21 test
Transient infantile hypertriglyceridemia and hepatosteatosis1 test
Triglyceride storage disease with ichthyosis1 test
Tuberous sclerosis 11 test
Tuberous sclerosis 21 test
Type 1 diabetes mellitus 201 test
Type 2 diabetes mellitus2 tests
Tyrosinase-positive oculocutaneous albinism6 tests
Tyrosinemia type I13 tests
Tyrosinemia type II7 tests
Tyrosinemia type III5 tests
UDPglucose-4-epimerase deficiency6 tests
Usher syndrome type 13 tests
Usher syndrome type 1C9 tests
Usher syndrome type 1D13 tests
Usher syndrome type 1F7 tests
Usher syndrome type 1G1 test
Usher syndrome type 2A7 tests
Usher syndrome type 2C6 tests
Usher syndrome type 2D5 tests
Usher syndrome type 39 tests
Usher syndrome type 3B1 test
VACTERL with hydrocephalus13 tests
Van Buchem disease type 21 test
Vanishing white matter disease6 tests
Variegate porphyria2 tests
Velocardiofacial syndrome2 tests
Very long chain acyl-CoA dehydrogenase deficiency15 tests
Vitamin B12-responsive methylmalonic acidemia, type cblDv24 tests
Vitamin D-dependent rickets type II with alopecia2 tests
Vitamin D-dependent rickets, type 11 test
Vitelliform macular dystrophy 26 tests
Von Hippel-Lindau syndrome13 tests
Weill-Marchesani syndrome 2, dominant5 tests
Werdnig-Hoffmann disease9 tests
Wilms tumor 114 tests
Wilson disease11 tests
Wilson-Turner syndrome1 test
Wiskott-Aldrich syndrome2 tests
Wolfram syndrome1 test
Wolfram syndrome 21 test
Wolfram-like syndrome1 test
Woolly hair-skin fragility syndrome1 test
Worth disease1 test
Wrinkly skin syndrome5 tests
X-linked agammaglobulinemia1 test
X-linked cone-rod dystrophy 11 test
X-linked cone-rod dystrophy 31 test
X-linked distal spinal muscular atrophy type 35 tests
X-linked erythropoietic protoporphyria1 test
X-linked ichthyosis with steryl-sulfatase deficiency1 test
X-linked intellectual disability-psychosis-macroorchidism syndrome7 tests
X-linked lissencephaly with abnormal genitalia6 tests
X-linked mixed hearing loss with perilymphatic gusher3 tests
X-linked severe combined immunodeficiency4 tests
X-linked sideroblastic anemia 11 test
X-linked sideroblastic anemia with ataxia1 test
alpha Thalassemia6 tests
beta Thalassemia8 tests