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CTGA Database Listing
Arab Genomic Studies
Records found: 2613 Sort by:
  • Factor XI Deficiency
    OMIM # 612416
    F11 Deficiency, Plasma Thromboplastin Antecedent Deficiency, PTA Deficiency, Rosenthal Syndrome
  • Mitochondrial DNA Depletion Syndrome 11
    OMIM # 615084
    MTDPS11
  • Mitochondrial Genome Maintenance Exonuclease 1
    OMIM # 615076
    MGME1
  • Mitochondrial Complex III Deficiency, Nuclear Type 6
    OMIM # 615453
    MC3DN6
  • Cytochrome C1
    OMIM # 123980
    CYC1
  • 1-@Acylglycerol-3-Phosphate O-Acyltransferase 2
    OMIM # 603100
    AGPAT2 , Lysophosphatidic Acid Acyltransferase-Beta, LPAAT-Beta,
  • Microcephaly, Primary Autosomal Recessive, 1
    OMIM # 251200
    MCPH1
  • Gyrate Atrophy of Choroid and Retina
    OMIM # 258870
    GACR, Hyperornithinemia with Gyrate Atrophy of Choroid and Retina, HOGA, Gyrate Atrophy, Ornithine Aminotransferase Deficiency , OAT Deficiency, Ornithine Keto Acid Aminotransferase Deficiency , OKT Deficiency, Ornithine-Delta-Aminotransferase Deficiency
  • Gaucher Disease, Type I
    OMIM # 230800
    GD I, Gaucher Disease, Noncerebral Juvenile, Glucocerebrosidase Deficiency, Acid Beta-Glucosidase Deficiency, GBA Deficiency,
  • Ornithine Aminotransferase
    OMIM # 613349
    OAT, Ornithine Keto Acid Aminotransferase, OKT, Ornithine Delta-Aminotransferase
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