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CTGA Database Listing
Arab Genomic Studies
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  • Cytochrome b5 Reductase 3
    OMIM # 613213
    CYB5R3, B5R, NADH-Diaphorase 1, DIA1
  • Methemoglobinemia due to Deficiency of Methemoglobin Reductase
    OMIM # 250800
    NADH-Dependent Methemoglobin Reductase Deficiency, NADH-Cytochrome b5 Reductase Deficiency, Methemoglobinemia, Congenital, Autosomal Recessive, Methemoglobinemia Type I, Methemoglobinemia, Type II, NADH-Cytochrome b5 Reductase Deficiency, Type I, NADH-Ccytochrome b5 Reductase Deficiency, Type II,
  • Carbamoyl Phosphate Synthetase I
    OMIM # 608307
    CPS1, Venoocclusive Disease after Bone Marrow Transplantation, Susceptibility to
  • Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia due to
    OMIM # 237300
    Carbamoyl Phosphate Synthetase I Deficiency, CPS I Deficiency,
  • Excision-Repair Cross-Complementing, Group 8
    OMIM # 609412
    ERCC8, CSA Gene, CKN1 Gene
  • Cockayne Syndrome, Type A
    OMIM # 216400
    CSA, CKN1
  • Arginase, Liver
    OMIM # 608313
    ARG1
  • Argininemia
    OMIM # 207800
    Arginase Deficiency, Hyperargininemia, ARG1 Deficiency
  • Acetyl-CoA Acetyltransferase 1
    OMIM # 607809
    ACAT1, ACAT, Acetoacetyl-CoA Thiolase, Mitochondrial, T2, Mitochondrial Acetoacetyl-CoA Thiolase, MAT
  • Alpha-Methylacetoacetic Aciduria
    OMIM # 203750
    2-Methyl-3-Hydroxybutyric Acidemia, Beta-Ketothiolase Deficiency, Mitochondrial Acetoacetyl-CoA Thiolase Deficiency, MAT Deficiency, T2 Deficiency, 3-Oxothiolase Deficiency, 3-Ketothiolase Deficiency, 3-KTD Deficiency,
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