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CTGA Database Listing
Arab Genomic Studies
Records found: 2616 Sort by:
  • SC Phocomelia Syndrome
    OMIM # 269000
    SC-Pseudothalidomide Syndrome
  • Retinoblastoma
    OMIM # 180200
    RB1, RB
  • Pseudoxanthoma Elasticum
    OMIM # 264800
    PXE, Gronblad-Strandberg Syndrome
  • WD Repeat-Containing Protein 73
    OMIM # 616144
    WDR73, HSPC264,
  • Galloway-Mowat Syndrome 1
    OMIM # 251300
    Galloway Syndrome, Galloway-Mowat Syndrome, Nephrosis-Neuronal Dysmigration Syndrome, Nephrosis-Microcephaly Syndrome
  • Usher Syndrome, Type IC
    OMIM # 276904
    USH1C, Usher Syndrome, Type I, Acadian Variety
  • USH1C Gene
    OMIM # 605242
    USH1C, Harmonin, PDZ Domain-Containing Protein, 73-kD, PDZ73,
  • Thrombocytopenia 1
    OMIM # 313900
    THC1, THC, Thrombocytopenia, X-Linked , XLT, Thrombocytopenia, X-Linked, 1, Thrombocytopenia, X-Linked, Intermittent,
  • Smith-Lemli-Opitz Syndrome
    OMIM # 270400
    SLOS, SLO Syndrome, RSH Syndrome, Rutledge Lethal Multiple Congenital Anomaly Syndrome, Polydactyly, Sex Reversal, Renal Hypoplasia, and Unilobular Lung, Lethal Acrodysgenital Syndrome
  • 7-Dehydrocholesterol Reductase
    OMIM # 602858
    DHCR7, Sterol Delta-7-Reductase,
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