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CTGA Database Listing
Arab Genomic Studies
Records found: 2870 Sort by:
  • Thiopurines, Poor Metabolism of, 2
    OMIM # 616903
    THPM2, NUDT15 Deficiency
  • Nudix Hydrolase 15
    OMIM # 615792
    NUDT15, Nucleoside Diphosphate-Linked Moiety X Motif 15, Nudix Motif 15, MutT Homolog 2, MTH2
  • Adrenal Hypoplasia, Congenital
    OMIM # 300200
    AHC, Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism, AHCH, Addison Disease, X-Linked, AHX, AHC with HHG, Cytomegalic Adrenocortical Hypoplasia, AHC with Isolated Gonadotropin Deficiency, Adrenal Insufficiency, Progressive, and Hypogonadotropic Hypogonadism, Mineralocorticoid Deficiency, Isolated
  • Nuclear Receptor Subfamily 0, Group B, Member 1
    OMIM # 300473
    NR0B1, DSS-AHC Critical Region on the X Chromosome1, Gene 1, DAX1
  • Vitamin D Receptor
    OMIM # 601769
    VDR, 1,25-Dihydroxyvitamin D3 Receptor, Vitamin D Hormone Receptor,
  • Prostate Cancer
    OMIM # 176807
  • Cytochrome P450, Family 17, Subfamily A, Polypeptide 1
    OMIM # 609300
    CYP17A1, Steroid 17-Alpha-Monooxygenase Cytochrome P450, Subfamily XVII, CYP17, P450C17, S17AH, Steroid 17-Hydroxylase/17,20-Lyase
  • Glutamate Pyruvate Transaminase
    OMIM # 138200
    GPT, Glutamate Pyruvate Transaminase, Soluble Red Cell, GPT1, Glutamate Pyruvate Transaminase, Soluble Liver, Alanine Aminotransferase 1, AAT1, ALT1, Alanine Aminotransferase, Soluble
  • Macroglobulinemia, Waldenstrom, Susceptibility To, 1
    OMIM # 153600
    WM1, Macroglobulinemia, Waldenstrom, Somatic
  • Splenogonadal Fusion with Limb Defects and Micrognathia
    OMIM # 183300
    Splenogonadal Fusion Limb Defect Syndrome, SGFLD Syndrome
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