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CTGA Database Listing
Arab Genomic Studies
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  • Bile Acid Synthesis Defect, Congenital, 2
    OMIM # 235555
    CBAS2, Cholestasis with Delta(4)-3-Oxosteroid 5-Beta-Reductase Deficiency,
  • Aldo-Keto Reductase Family 1, Member D1
    OMIM # 604741
    AKR1D1, Delta(4)-3-Oxosteroid 5-Beta-Reductase, Steroid 5-Beta-Reductase, SRD5B1, 5-Beta-Reductase
  • Dermatitis, Atopic
    OMIM # 603165
    ATOD, Eczema, Atopic, Dermatitis, Atopic, 1, ATOD1
  • Focal Segmental Glomerulosclerosis 1
    OMIM # 603278
    FSGS1, Glomerulosclerosis, Focal Segmental, 1, Glomerulosclerosis, Focal Segmental, FSGS
  • Microvascular Complications of Diabetes, Susceptibility to, 1
    OMIM # 603933
    Proliferative Retinopathy, Diabetic, Susceptibility to, Nonproliferative Retinopathy, Diabetic, Susceptibility to, Microvascular Complications of Diabetes, Susceptibility to, Microvascular Complications of Diabetes, Protection from, Nephropathy, Diabetic, Susceptibility to, End-Stage Renal Disease, Diabetic, Susceptibility to, Proliferative Retinopathy, Diabetic, Susceptibility to, Nonproliferative Retinopathy, Diabetic, Susceptibility to, Neuropathy, Diabetic, Susceptibility to
  • Muscular Dystrophy, Congenital, with Severe Central Nervous System Atrophy and Absence of Large Myelinated Fibers
    OMIM # 601170
  • Rheumatoid Arthritis
    OMIM # 180300
    RA
  • EVC Ciliary Complex Subunit 2
    OMIM # 607261
    EVC2, Limbin, LBN
  • EvC ciliary complex subunit 1
    OMIM # 604831
    EVC, EVC1,
  • Ellis-van Creveld Syndrome
    OMIM # 225500
    EVC, Chondroectodermal Dysplasia, Mesoectodermal Dysplasia,
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