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CTGA Database Listing
Arab Genomic Studies
Records found: 2477 Sort by:
  • Pericentrin
    OMIM # 605925
    PCNT, Kendrin, KEN, Pericentrin 2, Pericentrin B,
  • Microcephalic Osteodysplastic Primordial Dwarfism, Type II
    OMIM # 210720
    MOPD II, MOPD2, Osteodysplastic Primordial Dwarfism, Type II, Majewski Osteodysplastic Primordial Dwarfism, Type II
  • ATP-Binding Cassette, Subfamily D, Member 1
    OMIM # 300371
    ABCD1, Adrenoleukodystrophy Protein, ALDP,
  • Adrenoleukodystrophy
    OMIM # 300100
    ALD, Addison Disease and Cerebral Sclerosis, Adrenomyeloneuropathy, AMN, Siemerling-Creutzfeldt Disease, Bronze Schilder Disease, Melanodermic Leukodystrophy,
  • Androgen Receptor
    OMIM # 313700
    AR; Dihydrotestosterone Receptor, DHTR, Nuclear Receptor Subfamily 3, Group C, Member 4, NR3C4
  • Androgen Insensitivity Syndrome
    OMIM # 300068
    AIS, Testicular Feminization Syndrome, TFM, Androgen Receptor Deficiency, AR Deficiency, Dihydrotestosterone Receptor Deficiency, DHTR Deficiency
  • Xanthinuria, Type I
    OMIM # 278300
    Xanthine Dehydrogenase Deficiency, XDH Deficiency, Xanthine Oxidase Deficiency,
  • Dymeclin
    OMIM # 607461
    DYM
  • Dyggve-Melchior-Clausen Disease
    OMIM # 223800
    DMC
  • ATPase, Cu(2+)-Transporting, Beta Polypeptide
    OMIM # 606882
    ATP7B
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