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Pediatric/Medical Genetics, Ministry of Health (Qatif Central Hospital), EHC/MOH

General information

Pediatric/Medical Genetics, Ministry of Health, EHC/MOH
Qatif Central Hospital
Dhahran Jubail Branch Rd
Qatif
Ash Sharqiyah
Saudi Arabia - 4312

Organization ID: 508864

Personnel

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 53

Gene

GeneSubmissionsLast Updated
ALDH18A11Feb 10, 2024
ALG121Oct 22, 2023
AMT1Dec 21, 2022
ASS11Dec 21, 2022
ATAD11Nov 28, 2023
BCKDHB1Mar 7, 2023
BRAF1Sep 23, 2023
CACNA1S1Oct 27, 2023
CERT11Jun 7, 2023
COL4A21Feb 21, 2023
CRX1Jan 9, 2023
CSPP11Feb 4, 2023
EDEM31Dec 14, 2022
ELAC21Dec 21, 2022
FARS21Aug 12, 2023
FBP11Feb 19, 2023
FGFR31Mar 5, 2024
FUCA11Sep 8, 2023
GAA2Feb 2, 2023
GALC1Aug 17, 2023
GALT1Sep 23, 2023
GNS1Dec 22, 2023
HIBCH1Dec 21, 2022
LAMA21Oct 27, 2023
LOC1061130361Jan 3, 2023
MOGS1Jun 21, 2023
MYPN1Dec 21, 2022
NF11Jan 3, 2023
NFIX1Feb 21, 2023
NSD21Jul 4, 2023
NUP2051Mar 8, 2023
PCCA1Dec 13, 2022
PGAP11May 19, 2023
PGAP31Dec 12, 2022
PGK11Feb 21, 2023
PGM11Jan 31, 2023
PIGA1Nov 4, 2023
PPIB1Feb 5, 2023
PRX1Jan 9, 2023
PSMD121Feb 3, 2024
PTEN1Oct 28, 2023
RAF11Dec 12, 2022
SLC16A11Jan 9, 2023
SLC16A1-AS11Jan 9, 2023
SLC18A21Dec 21, 2022
SLC22A51Jun 22, 2023
SMPD11Jul 22, 2023
SNX221Feb 5, 2023
SRCAP1Dec 13, 2022
STAG11Aug 17, 2023
TTN2Dec 22, 2023
TTN-AS12Dec 22, 2023
UGT1A1Feb 25, 2024
UGT1A11Feb 25, 2024
UGT1A101Feb 25, 2024
UGT1A31Feb 25, 2024
UGT1A41Feb 25, 2024
UGT1A51Feb 25, 2024
UGT1A61Feb 25, 2024
UGT1A71Feb 25, 2024
UGT1A81Feb 25, 2024
UGT1A91Feb 25, 2024
ZNF1421Jun 22, 2023
ZNF2921Nov 4, 2023

Condition

NameSubmissionsLast Updated
ALDH18A1-related de Barsy syndrome1Feb 10, 2024
ALG12-congenital disorder of glycosylation1Oct 22, 2023
Autosomal recessive limb-girdle muscular dystrophy type 2J2Dec 22, 2023
Bannayan-Riley-Ruvalcaba syndrome1Oct 28, 2023
Beta-hydroxyisobutyryl-CoA deacylase deficiency1Dec 21, 2022
Camptodactyly-tall stature-scoliosis-hearing loss syndrome1Mar 5, 2024
Cardiofaciocutaneous syndrome 11Sep 23, 2023
Charcot-Marie-Tooth disease type 4F1Jan 9, 2023
Citrullinemia type I1Dec 21, 2022
Combined oxidative phosphorylation defect type 171Dec 21, 2022
Congenital disorder of glycosylation, type 2v1Dec 14, 2022
Congenital myopathy 181Oct 27, 2023
Crigler-Najjar syndrome type 11Feb 25, 2024
Crigler-Najjar syndrome, type II1Feb 25, 2024
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase1Sep 23, 2023
Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities1Dec 13, 2022
Dilated cardiomyopathy 1NN1Dec 12, 2022
Fructose-biphosphatase deficiency1Feb 19, 2023
Fucosidosis1Sep 8, 2023
Galactosylceramide beta-galactosidase deficiency1Aug 17, 2023
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency1Feb 21, 2023
Glycogen storage disease, type II2Feb 2, 2023
Hemorrhage, intracerebral, susceptibility to1Feb 21, 2023
Hereditary spastic paraplegia 771Aug 12, 2023
Hyperekplexia 41Nov 28, 2023
Hyperphosphatasia with intellectual disability syndrome 41Dec 12, 2022
Intellectual developmental disorder, autosomal dominant 641Nov 4, 2023
Intellectual disability, autosomal dominant 341Jun 7, 2023
Intellectual disability, autosomal dominant 471Aug 17, 2023
Intellectual disability, autosomal recessive 421May 19, 2023
Joubert syndrome 211Feb 4, 2023
Ketoacidosis due to monocarboxylate transporter-1 deficiency1Jan 9, 2023
Leber congenital amaurosis 71Jan 9, 2023
Lucey-Driscoll syndrome1Feb 25, 2024
MOGS-congenital disorder of glycosylation1Jun 21, 2023
MYPN-related myopathy1Dec 21, 2022
Malan overgrowth syndrome1Feb 21, 2023
Maple syrup urine disease1Mar 7, 2023
Merosin deficient congenital muscular dystrophy1Oct 27, 2023
Mucopolysaccharidosis, MPS-III-D1Dec 22, 2023
Multiple congenital anomalies-hypotonia-seizures syndrome 21Nov 4, 2023
Muscular dystrophy, limb-girdle, autosomal recessive 231Oct 27, 2023
Nephrotic syndrome, type 131Mar 8, 2023
Neurodevelopmental disorder with impaired speech and hyperkinetic movements1Jun 22, 2023
Neurofibromatosis, type 11Jan 3, 2023
Niemann-Pick disease, type B1Jul 22, 2023
Non-ketotic hyperglycinemia1Dec 21, 2022
Osteogenesis imperfecta type 91Feb 5, 2023
PGM1-congenital disorder of glycosylation1Jan 31, 2023
Parkinsonism-dystonia, infantile, 21Dec 21, 2022
Propionic acidemia1Dec 13, 2022
Rauch-Steindl syndrome1Jul 4, 2023
Renal carnitine transport defect1Jun 22, 2023
Stankiewicz-Isidor syndrome1Feb 3, 2024