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CTGA Database Listing
Arab Genomic Studies
Records found: 2870 Sort by:
  • Pendred Syndrome
    OMIM # 274600
    PDS, Deafness with Goiter, Goiter-Deafness Syndrome, Thyroid Hormonogenesis, Genetic Defect In, 2B, Hypothyroidism, Congenital, due to Dyshormonogenesis, 2B, Thyroid Hormone Organification Defect IIB
  • Transaldolase Deficiency
    OMIM # 606003
    Eyaid Syndrome, TALDO Deficiency
  • Transaldolase 1
    OMIM # 602063
    TALDO1
  • 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
  • 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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