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CTGA Database Listing
Arab Genomic Studies
Records found: 2746 Sort by:
  • HFE Gene
    OMIM # 613609
    HFE
  • Breast Cancer
    OMIM # 114480
    Breast Cancer, Familial, Breast Cancer, Familial Male
  • Breast Cancer 1 Gene
    OMIM # 113705
    BRCA1,
  • Lynch Syndrome I
    OMIM # 120435
    Colorectal Cancer, Hereditary Nonpolyposis, Type 1, HNPCC1, Colon Cancer, Familial Nonpolyposis, Type 1, FCC1, COCA1, Lynch Syndrome II
  • Arthrogryposis, Distal, Type 2A
    OMIM # 193700
    DA2A, Freeman-Sheldon Syndrome, FSS, Whistling Face-Windmill Vane Hand Syndrome, Craniocarpotarsal Dystrophy, Craniocarpotarsal Dysplasia
  • Von Hippel-Lindau Syndrome
    OMIM # 193300
    Von Hippel-Lindau Syndrome, Modifiers of, VHL
  • Cytochrome P450, Subfamily IIC, Polypeptide 19
    OMIM # 124020
    CYP2C19, Mephenytoin 4-Prime-Hydroxylase, P450C2C, CYP2C,
  • Glutaric Acidemia I
    OMIM # 231670
    Glutaric Aciduria I, GA I, Glutaryl-CoA Dehydrogenase Deficiency, GDD
  • Alkaptonuria
    OMIM # 203500
    AKU, Homogentisic Acid Oxidase Deficiency,
  • Acetyl-CoA Acetyltransferase 1
    OMIM # 607809
    ACAT1, ACAT, Acetoacetyl-CoA Thiolase, Mitochondrial, T2, Mitochondrial Acetoacetyl-CoA Thiolase, MAT
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