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CTGA Database Listing
Arab Genomic Studies
Records found: 2410 Sort by:
  • 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
  • Galactosamine-6-Sulfate Sulfatase
    OMIM # 612222
    GALNS, N-Acetylgalactosamine-Sulfate Sulfatase
  • Eukaryotic Translation Initiation Factor 2-Alpha Kinase 3
    OMIM # 604032
    EIF2AK3 , Pancreatic EIF2-Alpha Kinase, PEK, PERK, Heme-Regulated EIF2-Alpha Kinase, HRI
  • ATP-Binding Cassette, Subfamily C, Member 8
    OMIM # 600509
    ABCC8, Sulfonylurea Receptor, SUR, SUR1, Sulfonylurea Receptor, Beta-Cell High-Affinity,
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