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CTGA Database Listing
Arab Genomic Studies
Records found: 2804 Sort by:
  • Cytochrome P450, Subfamily IIC, Polypeptide 19
    OMIM # 124020
    CYP2C19, Mephenytoin 4-Prime-Hydroxylase, P450C2C, CYP2C,
  • Vitamin K Epoxide Reductase Complex, Subunit 1
    OMIM # 608547
    VKORC1, VKOR, FLJ00289
  • Cytochrome P450, Subfamily IIC, Polypeptide 9
    OMIM # 601130
    CYP2C9
  • Cytochrome P450, Subfamily IIB, Polypeptide 6
    OMIM # 123930
    cYP2B6, Cytochrome P450, Phenobarbitol-Inducible
  • Cytochrome P450, Subfamily A, Polypeptide 1
    OMIM # 108330
    CYP1A1, Cytochrome P450, Aromatic Compound-Inducible, Aryl Hydrocarbon Hydroxylase, AHH, Flavoprotein-Linked Monooxygenase, Cytochrome P1-450, Dioxin-Inducible, Cytochrome P1-450, Inducible By 2,3,7,8-Tetrachlorodibenzo-P-Dioxin, Tcdd-Inducible Cytochrome P1-450, P450DX, Polycyclic Aromatic Compound-Inducible P450
  • Hymen, Imperforate
    OMIM # 237100
  • Transmembrane Protein 67
    OMIM # 609884
    TMEM67, MKS3 Gene, MKS3, Meckelin
  • Meckel Syndrome, Type 3
    OMIM # 607361
    MKS3, Meckel-Gruber Syndrome, Type 3
  • Holocarboxylase Synthetase Deficiency
    OMIM # 253270
    MCD, Holocarboxylase Synthetase Deficiency, HLCS Deficiency, Multiple Carboxylase Deficiency, Neonatal Form, Holocarboxylase Synthetase, HLCS, Multiple Carboxylase Deficiency, Eraly Onset,
  • Hydatidiform Mole, Recurrent, 1
    OMIM # 231090
    HYDM1, Hydatidiform Mole, HYDM, Hydatidiform Mole, Complete, CHM, Gestational Trophoblastic Disease,
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