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CTGA Database Listing
Arab Genomic Studies
Records found: 2423 Sort by:
  • Cornelia de Lange Syndrome 4
    OMIM # 614701
    CDLS4
  • Rad21, S. Pombe, Homolog of
    OMIM # 606462
    RAD21
  • 3-@Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase (*)
    OMIM # 607764
    HSD3B7
  • Bile Acid Synthesis Defect, Congenital, 1
    OMIM # 607765
    CBAS1, 3-Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase Deficiency
  • Bronchiectasis with or without Elevated Sweat Chloride 1
    OMIM # 211400
    BESC1, Cystic Fibrosis-Like Syndrome, Atypical Cystic Fibrosis
  • Carbonic Anhydrase XII
    OMIM # 603263
    CA12
  • Autism, Susceptibility to, 18
    OMIM # 615032
    AUTS18
  • Chromodomain Helicase DNA-Binding Protein 8
    OMIM # 610528
    CHD8, Axis Duplication Inhibitor, DUPLIN, KIAA1564
  • Arachidonate 12-Lipoxygenase, R Type
    OMIM # 603741
    ALOX12B
  • Adenylate Kinase 5
    OMIM # 608009
    AK5
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