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CTGA Database Listing
Arab Genomic Studies
Records found: 2616 Sort by:
  • Major Histocompatibility Complex, Class I, A
    OMIM # 142800
    HLA-A, HLA-A Histocompatibility Type
  • Transcription Factor 7-Like 2
    OMIM # 602228
    TCF7L2, T-Cell Transcription Factor 4, TCF4
  • Diabetes Mellitus, Noninsulin-Dependent
    OMIM # 125853
    NIDDM, Diabetes Mellitus, Type II, T2D, Noninsulin-Dependent Diabetes Mellitus, Maturity-Onset Diabetes, Insulin Resistance, Susceptibility to
  • Protein Kinase, Lysine-Deficient 1
    OMIM # 605232
    WNK1 , Prostrate-Derived Sterile 20-Like Kinase , PSK, PRKWNK1, KDP, KIAA0344
  • Neuropathy, Hereditary Sensory and Autonomic, Type II
    OMIM # 201300
    HSAN2, HSAN II, Neuropathy, Hereditary Sensory, Type II, HSN2, HSN II, Acroosteolysis, Neurogenic, Acroosteolysis, Giaccai Type, Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive, Morvan Disease, Neuropathy, Progressive Sensory, of Children, Neuropathy, Congenital Sensory,
  • Patatin-Like Phospholipase Domain-Containing Protein 2
    OMIM # 609059
    PNPLA2, Adipose Triglyceride Lipase, ATGL, Desnutrin , Transport-Secretion Protein 2 , TTS2, TTS2.2, Phospholipase A2, Calcium-Independent, Zeta , IPLA2-Zeta
  • Neutral Lipid Storage Disease with Myopathy
    OMIM # 610717
    NLSDM, Neutral Lipid Storage Disease without Ichthyosis
  • Megaloblastic Anemia 1
    OMIM # 261100
    MGA1, Imerslund-Grasbeck Syndrome, IGS, Pernicious Anemia, Juvenile, due to Selective Intestinal Malabsorption of Vitamin B12, with Proteinuria, Enterocyte Cobalamin Malabsorption Enterocyte Intrinsic Factor Receptor, Defect of
  • Cubilin
    OMIM # 602997
    CUBN, Intrinsic Factor-Cobalamin Receptor, Intestinal Intrinsic Factor Receptor, IFCR
  • FYVE, RhoGEF and PH Domain-Containing Protein 4
    OMIM # 611104
    FGD4
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