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CTGA Database Listing
Arab Genomic Studies
Records found: 2614 Sort by:
  • 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,
  • Steroid 5-Alpha-Reductase 2
    OMIM # 607306
    SRD5A2
  • Pseudovaginal Perineoscrotal Hypospadias
    OMIM # 264600
    PPSH, Male Pseudohermaphroditism due to 5-Alpha-Reductase Deficiency, Familial Incomplete Male Pseudohermaphroditism, Type 2, 5-Alpha-Reductase 2 Deficiency
  • Prolidase Deficiency
    OMIM # 170100
  • POF1B Gene
    OMIM # 300603
    POF1B, FLJ22792, Actin-Binding Protein, 34-KD
  • Premature Ovarian Failure 2B
    OMIM # 300604
    POF2B
  • Porphyria, Congenital Erythropoietic
    OMIM # 263700
    CEP, Gunther Disease, Uroporphyrinogen III Synthase, Deficiency of, UROS Deficiency
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