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CTGA Database Listing
Arab Genomic Studies
Records found: 2510 Sort by:
  • Hemoglobin, Gamma G
    OMIM # 142250
    HBG2, Hemoglobin--Gamma Locus, 136 Glycine
  • Hemoglobin - Beta Locus
    OMIM # 141900
    HBB, Beta-Thalassemia, Beta-Thalassemias, Methemoglobinemia, Beta-Globin Type, Erythremia, Beta-Globin Type, Cooley's Anemia
  • Hemoglobin - Alpha Locus 1
    OMIM # 141800
    HBA1, 3-Prime @Alpha-Globin Gene, Minor Alpha-Globin Locus, Alpha-Thalassemia, Methemoglobinemia, Alpha-Globin Type, Erythremia, Alpha-Globin Type
  • Fetal Hemoglobin Quantitative Trait Locus 1
    OMIM # 141749
    HBFQTL1, Hemoglobin F, Hereditary Persistence of,, Hereditary Persistence of Fetal Hemoglobin, HB gene cluster-related, HPFH, Delta-Beta Thalassemia
  • 1-@Acylglycerol-3-Phosphate O-Acyltransferase 2
    OMIM # 603100
    AGPAT2 , Lysophosphatidic Acid Acyltransferase-Beta, LPAAT-Beta,
  • 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,
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