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CTGA Database Listing
Arab Genomic Studies
Records found: 2828 Sort by:
  • Solute Carrier Family 26, Member 4
    OMIM # 605646
    SLC26A4, Pendrin, PDS Gene,
  • Cold-Induced Sweating Syndrome 1
    OMIM # 272430
    CISS1, Crisponi Syndrome, Sohar-Crisponi Syndrome, Muscle Contractions, Tetanoform, with Characteristic Face, Camptodactyly, Hyperthermia, and Sudden Death
  • Cytokine Receptor-Like Factor 1
    OMIM # 604237
    CRLF1, CLF1, NR6
  • Propionyl-CoA Carboxylase, Beta Subunit
    OMIM # 232050
    PCCB, PCCB Complementation Group
  • Propionic Acidemia
    OMIM # 606054
    Propionyl-CoA Carboxylase Deficiency, PCC Deficiency, Glycinemia, Ketotic, Hyperglycinemia with Ketoacidosis and Leukopenia, Ketotic Hyperglycinemia,
  • Propionyl-CoA Carboxylase, Alpha Subunit
    OMIM # 232000
    PCCA, PCCA Complementation Group
  • Transglutaminase 1
    OMIM # 190195
    TGM1, Transglutaminase, Keratinocyte, TGK, Transglutaminase, Epidermal Type I,
  • Ichthyosis, Lamellar, 1
    OMIM # 242300
    LI1, Ichthyosis Congenita, Lamellar Exfoliation of Newborn, Desquamation of Newborn, Collodion Fetus, Lamellar Ichthyosis, LI, Lamellar Ichthyosis, Type 1, Ichthyosis Congenita II, ICR2, Self-Healing Collodion Baby,
  • Anorexia Nervosa, Susceptibility to, 1
    OMIM # 606788
    ANON1, AN
  • Polymicrogyria, Bilateral Frontoparietal
    OMIM # 606854
    BFPP, Cerebellar Ataxia with Neuronal Migration Defect,
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