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Pediatric Genetics Clinic (Sheba Medical Center)

General information

Pediatric Genetics Clinic
Sheba Medical Center
Ramat Gan
Israel - 52621

Organization ID: 508051

Assertion criteria

Level: Assertion criteria not provided

    Summary of submissions to ClinVar

    Total submissions: 126

    Gene

    GeneSubmissionsLast Updated
    AHDC12Jun 7, 2021
    ANKRD111Jun 7, 2021
    ARID1A1Jun 7, 2021
    ARID1B3Jun 7, 2021
    AUTS21Jun 7, 2021
    BCL11B1Jun 7, 2021
    BRPF11Jun 7, 2021
    CACNA1C1Jun 7, 2021
    CASK1Jun 7, 2021
    CCDC391Apr 29, 2021
    CCDC401Apr 29, 2021
    CDK131Jun 7, 2021
    CELSR11Apr 29, 2021
    CERS11Apr 29, 2021
    CFAP2981Apr 29, 2021
    CFAP298-TCP10L1Apr 29, 2021
    CFAP3001Apr 29, 2021
    CFAP461Apr 29, 2021
    CFAP532Apr 29, 2021
    CHAMP11Jun 7, 2021
    CLCN41Jun 7, 2021
    CNTNAP21Jun 7, 2021
    COL1A11Jun 7, 2021
    CTNNB11Jun 7, 2021
    CUL4B1Jun 7, 2021
    DAND51Apr 29, 2021
    DCX1Jun 7, 2021
    DDX3X1Jun 7, 2021
    DLG41Jun 7, 2021
    DNAAF11Apr 29, 2021
    DNAAF111Apr 29, 2021
    DNAH52Apr 29, 2021
    DNAH61Apr 29, 2021
    DYNC1H11Jun 7, 2021
    EFTUD21Jun 7, 2021
    EPG51Jun 7, 2021
    EPHB41Jun 7, 2021
    EVC21Jun 7, 2021
    FGFR21Jun 7, 2021
    FOXP12Jun 7, 2021
    FOXP21Jun 7, 2021
    GABRB31Jun 7, 2021
    GDF11Apr 29, 2021
    GRIN2B1Jun 7, 2021
    HDAC81Jun 7, 2021
    KANSL12Jun 7, 2021
    KCNMA12Jun 7, 2021
    KCNMA1-AS11Jun 7, 2021
    KCNQ22Jun 7, 2021
    KCNQ31Jun 7, 2021
    KCNT11Jun 7, 2021
    KMT2A1Jun 7, 2021
    KMT2D1Jun 7, 2021
    KMT5B2Jun 7, 2021
    LOC1027240581Jun 7, 2021
    LOC1268066581Jun 7, 2021
    LOC1268601241Jun 7, 2021
    LOC1268620601Jun 7, 2021
    LOC1268624791Jun 7, 2021
    LOC1299980211Jun 7, 2021
    MAP2K12Jun 7, 2021
    MEA12Jun 7, 2021
    MED13L2Jun 7, 2021
    MYT1L1Jun 7, 2021
    NEXMIF1Jun 7, 2021
    NF11Jun 7, 2021
    NSD11Jun 7, 2021
    ODAD41Apr 29, 2021
    OPHN12Jun 7, 2021
    PACS11Jun 7, 2021
    PAFAH1B11Jun 7, 2021
    PBX11Jun 7, 2021
    PKD1L11Apr 29, 2021
    POGZ1Jun 7, 2021
    PPP2CA1Jun 7, 2021
    PPP2R5D2Jun 7, 2021
    PTPN111Jun 7, 2021
    RB11Jun 7, 2021
    RPS6KA31Jun 7, 2021
    SATB21Jun 7, 2021
    SCN1A1Jun 7, 2021
    SCN2A1Jun 7, 2021
    SCN8A1Jun 7, 2021
    SCUBE31Jun 7, 2021
    SETBP11Jun 7, 2021
    SETD1A1Jun 7, 2021
    SETD21Jun 7, 2021
    SHH1Jun 7, 2021
    SLC1A41Jun 7, 2021
    SMAD41Jun 7, 2021
    SMC1A3Jun 7, 2021
    SNHG141Jun 7, 2021
    SOX91Jun 7, 2021
    SSR41Jun 7, 2021
    STXBP12Jun 7, 2021
    SYNGAP11Jun 7, 2021
    SYNGAP1-AS11Jun 7, 2021
    SYT11Jun 7, 2021
    TBL1XR11Jun 7, 2021
    TBR11Jun 7, 2021
    TCF202Jun 7, 2021
    TCF42Jun 7, 2021
    TRIP121Jun 7, 2021
    TRMT12Jun 7, 2021
    TRMT10A1Jun 7, 2021
    TSEN541Jun 7, 2021
    TSPAN71Jun 7, 2021
    TUBA1A1Jun 7, 2021
    TWIST11Jun 7, 2021
    UBE3A1Jun 7, 2021
    USP71Jun 7, 2021
    VPS13B2Jun 7, 2021
    WDR451Jun 7, 2021
    YWHAG1Jun 7, 2021
    ZC4H21Jun 7, 2021
    ZEB21Jun 7, 2021
    ZSWIM61Jun 7, 2021

    Condition

    NameSubmissionsLast Updated
    AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome2Jun 7, 2021
    Angelman syndrome1Jun 7, 2021
    Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis1Jun 7, 2021
    Autism spectrum disorder due to AUTS2 deficiency1Jun 7, 2021
    Autism, susceptibility to, 51Jun 7, 2021
    Café-au-lait macules with pulmonary stenosis1Jun 7, 2021
    Camptomelic dysplasia1Jun 7, 2021
    Capillary malformation-arteriovenous malformation 21Jun 7, 2021
    Cardiac anomalies - developmental delay - facial dysmorphism syndrome2Jun 7, 2021
    Cardiofaciocutaneous syndrome 32Jun 7, 2021
    Childhood apraxia of speech1Jun 7, 2021
    Chromosome 2q32-q33 deletion syndrome1Jun 7, 2021
    Clark-Baraitser syndrome1Jun 7, 2021
    Coffin-Lowry syndrome1Jun 7, 2021
    Coffin-Siris syndrome 14Jun 7, 2021
    Cohen syndrome2Jun 7, 2021
    Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay1Jun 7, 2021
    Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder1Jun 7, 2021
    Congenital muscular hypertrophy-cerebral syndrome3Jun 7, 2021
    Cornelia de Lange syndrome 51Jun 7, 2021
    Cortical dysplasia-focal epilepsy syndrome1Jun 7, 2021
    Developmental and epileptic encephalopathy, 111Jun 7, 2021
    Developmental and epileptic encephalopathy, 131Jun 7, 2021
    Developmental and epileptic encephalopathy, 141Jun 7, 2021
    Developmental and epileptic encephalopathy, 42Jun 7, 2021
    Developmental and epileptic encephalopathy, 431Jun 7, 2021
    Developmental and epileptic encephalopathy, 561Jun 7, 2021
    Developmental and epileptic encephalopathy, 72Jun 7, 2021
    Developmental delay with variable intellectual impairment and behavioral abnormalities2Jun 7, 2021
    Ellis-van Creveld syndrome1Jun 7, 2021
    Epilepsy, early-onset, with or without developmental delay1Jun 7, 2021
    Generalized epilepsy-paroxysmal dyskinesia syndrome2Jun 7, 2021
    Hao-Fountain syndrome1Jun 7, 2021
    Heterotaxy17Apr 29, 2021
    Hogue-Janssens syndrome 12Jun 7, 2021
    Houge-Janssens syndrome 31Jun 7, 2021
    Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome1Jun 7, 2021
    Intellectual developmental disorder 621Jun 7, 2021
    Intellectual developmental disorder with dysmorphic facies and ptosis1Jun 7, 2021
    Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities1Jun 7, 2021
    Intellectual developmental disorder, autosomal recessive 682Jun 7, 2021
    Intellectual disability1Jun 7, 2021
    Intellectual disability, X-linked 1021Jun 7, 2021
    Intellectual disability, X-linked 491Jun 7, 2021
    Intellectual disability, X-linked 581Jun 7, 2021
    Intellectual disability, autosomal dominant 131Jun 7, 2021
    Intellectual disability, autosomal dominant 291Jun 7, 2021
    Intellectual disability, autosomal dominant 391Jun 7, 2021
    Intellectual disability, autosomal dominant 401Jun 7, 2021
    Intellectual disability, autosomal dominant 411Jun 7, 2021
    Intellectual disability, autosomal dominant 51Jun 7, 2021
    Intellectual disability, autosomal dominant 512Jun 7, 2021
    Intellectual disability, autosomal dominant 61Jun 7, 2021
    Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome1Jun 7, 2021
    Intellectual disability-severe speech delay-mild dysmorphism syndrome2Jun 7, 2021
    KBG syndrome1Jun 7, 2021
    Kabuki syndrome 11Jun 7, 2021
    Koolen-de Vries syndrome2Jun 7, 2021
    Lissencephaly due to LIS1 mutation1Jun 7, 2021
    Lissencephaly due to TUBA1A mutation1Jun 7, 2021
    Lissencephaly type 1 due to doublecortin gene mutation1Jun 7, 2021
    Luscan-Lumish syndrome1Jun 7, 2021
    Mandibulofacial dysostosis-microcephaly syndrome1Jun 7, 2021
    Microcephaly, short stature, and impaired glucose metabolism 11Jun 7, 2021
    Mowat-Wilson syndrome1Jun 7, 2021
    Myhre syndrome1Jun 7, 2021
    Neurodegeneration with brain iron accumulation 51Jun 7, 2021
    Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features1Jun 7, 2021
    Noonan syndrome 11Jun 7, 2021
    Osteogenesis imperfecta type III1Jun 7, 2021
    Partial agenesis of the corpus callosum1Jun 7, 2021
    Pitt-Hopkins syndrome2Jun 7, 2021
    Pontocerebellar hypoplasia type 2A1Jun 7, 2021
    Retinoblastoma1Jun 7, 2021
    SSR4-congenital disorder of glycosylation1Jun 7, 2021
    Saethre-Chotzen syndrome1Jun 7, 2021
    Schuurs-Hoeijmakers syndrome1Jun 7, 2021
    Severe intellectual disability-progressive spastic diplegia syndrome1Jun 7, 2021
    Severe myoclonic epilepsy in infancy1Jun 7, 2021
    Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 21Jun 7, 2021
    Sotos syndrome1Jun 7, 2021
    Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome1Jun 7, 2021
    Syndromic X-linked intellectual disability Najm type1Jun 7, 2021
    Timothy syndrome1Jun 7, 2021
    Vici syndrome1Jun 7, 2021
    Wieacker-Wolff syndrome, female-restricted1Jun 7, 2021
    Wiedemann-Steiner syndrome1Jun 7, 2021
    X-linked intellectual disability Cabezas type1Jun 7, 2021
    X-linked intellectual disability, Cantagrel type1Jun 7, 2021
    X-linked intellectual disability-cerebellar hypoplasia syndrome2Jun 7, 2021