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CTGA Database Listing
Arab Genomic Studies
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  • 17-@Beta Hydroxysteroid Dehydrogenase III Deficiency (*)
    OMIM # 264300
    17-@Ketosteroid Reductase Deficiency of Testis, 17-@KSR Deficiency, Neutral 17-Beta-Hydroxysteroid Oxidoreductase Deficiency, Pseudohermaphroditism, Male, with Gynecomastia, Polycystic Ovarian Disease due to 17-Ketosteroid Reductase Deficiency,
  • Glycoprotein Ib Platelet Subunit Beta
    OMIM # 138720
    GPIBB, Platelet Glycoprotein Ib Beta Chain, Truncated Platelet Membrane Glycoprotein Ib Beta, GP-Ib Beta ,
  • Bernard-Soulier Syndrome
    OMIM # 231200
    BSS, Bleeding Disorder, Platelet-Type, 1, BDPLT1, Platelet Glycoprotein Ib Deficiency, Glycoprotein Ib, Platelet, Deficiency of, Von Willebrand Factor Receptor Deficiency, Bernard-Soulier Syndrome, Type A1, Bernard-Soulier Syndrome, Type B, Bernard-Soulier Syndrome, Type C,
  • Hemifacial Atrophy, Progressive
    OMIM # 141300
    HFA, Parry-Romberg Syndrome
  • Hematuria, Benign Familial
    OMIM # 141200
    BFH, Thin-Basement-Membrane Nephropathy, Thin Membrane Nephropathy, TMN,
  • Hemangioma-Thrombocytopenia Syndrome
    OMIM # 141000
    Kasabach-Merritt Syndrome, KMS
  • Hashimoto Thyroiditis
    OMIM # 140300
    HT, Hashimoto Struma, Hypothyroidism, Autoimmune, Thyroid Autoantibodies,
  • Guillain-Barre Syndrome, Familial
    OMIM # 139393
    GBS, Polyneuropathy, Inflammatory Demyelinating, Acute, AIDP, Polyneuropathy, Inflammatory Demyelinating, Chronic, CIDP
  • Gray Platelet Syndrome
    OMIM # 139090
    GPS, Bleeding Disorder, Platelet-Type, 4, BDPLT4, Platelet Alpha-Granule Deficiency,
  • Glutathione Reductase
    OMIM # 138300
    GSR, Glutathione Reductase, Hemolytic Anemia due to Deficiency of, in Red Cells
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