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CTGA Database Listing
Arab Genomic Studies
Records found: 2441 Sort by:
  • Colorblindness, Partial, Deutan Series
    OMIM # 303800
    CBD, Deutan Colorblindness, DCB, Deuteranopia, Green Colorblindness,
  • Enhanced S-Cone Syndrome
    OMIM # 268100
    ESCS, Goldmann-Favre Syndrome, Retinoschisis with Early Hemeralopia, Favre Hyaloideoretinal Degeneration
  • Glutaric Acidemia I
    OMIM # 231670
    Glutaric Aciduria I, GA I, Glutaryl-CoA Dehydrogenase Deficiency, GDD
  • Fanconi-Bickel Syndrome; FBS
    OMIM # 227810
    Hepatorenal Glycogenosis with Renal Fanconi Syndrome, Hepatic Glycogenosis with Fanconi Nephropathy, Hepatic Glycogenosis with Amino Aciduria and Glucosuria, Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance, Pseudo-Phlorizin Diabetes, Glycogenosis, Fanconi Type, Glycogen Storage Disease XI,
  • Dandy-Walker Syndrome
    OMIM # 220200
    DWS, Dandy-Walker Malformation , DWM
  • Chediak-Higashi Syndrome
    OMIM # 214500
    CHS, Begnez-Cesar's Syndrome, Chediak-Steinbrinck-Higashi Syndrome, Leukocytic Anomaly Albinism, Natural Killer Lymphocytes, Defect in, Oculocutaneous Albinism, Chediak-Higashi Type
  • VATER Association
    OMIM # 192350
    VACTERL Association
  • Glutathione Reductase
    OMIM # 138300
    GSR, Glutathione Reductase, Hemolytic Anemia due to Deficiency of, in Red Cells
  • Apolipoprotein A-I
    OMIM # 107680
    APOA1, Apolipoprotein of High Density Lipoprotein, APOA1 Deficiency, APOA1/APOC3 Fusion Gene,
  • Sulfite Oxidase
    OMIM # 606887
    SUOX
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