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CTGA Database Listing
Arab Genomic Studies
Records found: 2744 Sort by:
  • Opioid Receptor, Mu-1
    OMIM # 600018
    OPRM1, OPRM, Mu Opioid Receptor, MOR, MOR1
  • Catechol-O-Methyltransferase
    OMIM # 116790
    COMT, Catechol-O-Methyltransferase Activity, Low, in Red Cells
  • Coarctation of Aorta
    OMIM # 120000
  • Tetralogy of Fallot
    OMIM # 187500
    TOF
  • Heart- and Neural Crest Derivatives-Expressed 2
    OMIM # 602407
    HAND2, HLH Transcription Factor HAND2, Deciduum, Heart, Autonomic Nervous System, Neural Crest-Derived, DHAND2, DHAND
  • Thyroid Carcinoma, Papillary
    OMIM # 188550
    Papillary Carcinoma of Thyroid , PACT, PTC, TPC, Familial Nonmedullary Thyroid Cancer, FNMTC, Nonmedullary Thyroid Carcinoma, NMTC,
  • V-RAF Murine Sarcoma Viral Oncogene Homolog B1
    OMIM # 164757
    Oncogene BRAF, BRAF1, RAFB1
  • Apolipoprotein E
    OMIM # 107741
    APOE, Apolipoprotein E, Deficiency or Defect of, Hyperlipoproteinemia, type 111, Dysbetalipoproteinemia due to Defect in Apolipoprotein E-d, Familial Hyperbeta- and Prebetalipoproteinemia, Familial Hypercholesterolemia with Hyperlipemia, Hyperlipemia with Familial Hypercholesterolemic Xanthomatosis, INCI, Broad-Betalipoproteinemia, Floating-Betalipoproteinemia, Coronary Artery Disease, Severe, Susceptibility to, Low Density Lipoprotein Cholesterol Level Quantitative Trait Locus 5, included, LDLCQ5
  • Deafness, Autosomal Recessive 13
    OMIM # 603098
    DFNB13
  • Warburg Micro Syndrome 1
    OMIM # 600118
    WARBM1, Micro Syndrome
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