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CTGA Database Listing
Arab Genomic Studies
Records found: 2791 Sort by:
  • Activating Transcription Factor 6
    OMIM # 605537
    ATF6, Activating Transcription Factor 6, Alpha, ATF6A
  • Sodium Channel, Voltage-Gated, Type V, Alpha Subunit
    OMIM # 600163
    SCN5A, NAV1.5
  • Long QT Syndrome 1
    OMIM # 192500
    LQT1, Ward-Romano Syndrome, WRS, Romano-Ward Syndrome, RWS, Ventricular Fibrillation with Prolonged QT Interval, Long QT Syndrome 1/2, LQT1/2, Long QT Syndrome 1, Acquired, Susceptibility to
  • Potassium Channel, Voltage-Gated, KQT-Like Subfamily, Member 1
    OMIM # 607542
    KCNQ1, Potassium Channel, Voltage-Gated, Shaker-Related Subfamily, Member 9, KVLQT1, KCNA9, KCNA8
  • Hemochromatosis
    OMIM # 235200
    HLAH, Hemochromatosis, Hereditary, HH, HFE Gene, HFE
  • HFE Gene
    OMIM # 613609
    HFE
  • Lynch Syndrome I
    OMIM # 120435
    Colorectal Cancer, Hereditary Nonpolyposis, Type 1, HNPCC1, Colon Cancer, Familial Nonpolyposis, Type 1, FCC1, COCA1, Lynch Syndrome II
  • Von Hippel-Lindau Syndrome
    OMIM # 193300
    Von Hippel-Lindau Syndrome, Modifiers of, VHL
  • Glutaric Acidemia I
    OMIM # 231670
    Glutaric Aciduria I, GA I, Glutaryl-CoA Dehydrogenase Deficiency, GDD
  • Alkaptonuria
    OMIM # 203500
    AKU, Homogentisic Acid Oxidase Deficiency,
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