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CTGA Database Listing
Arab Genomic Studies
Records found: 2746 Sort by:
  • Coagulation Factor II
    OMIM # 176930
    F2, Thrombin, Prothrombin, Factor II
  • Janus Kinase 2
    OMIM # 147796
    JAK2 , JAK2/ETV6 Fusion Gene
  • Budd-Chiari Syndrome
    OMIM # 600880
    BDCHS
  • Potassium Channel, Voltage-Gated, Subfamily H, Member 2
    OMIM # 152427
    KCNH2, Human Ether-A-Go-Go-Related Gene, HERG, Ether-A-Go-Go-Related Gene, Human, ERG1, KV11.1
  • Long QT Syndrome 2
    OMIM # 613688
    LQT2, Long QT Syndrome 2, Acquired, Susceptibility to, Long QT Syndrome 1/2, Digenic, LQT1/2, Digenic, Long QT Syndrome 2/3, Digenic, LQT2/3, Digenic, Long QT Syndrome 2/5, Digenic, LQT2/5, Digenic, Long QT Syndrome 2/9, Digenic, LQT2/9, Digenic
  • Vitamin D Receptor
    OMIM # 601769
    VDR, 1,25-Dihydroxyvitamin D3 Receptor, Vitamin D Hormone Receptor,
  • N-Acetyltransferase 1
    OMIM # 108345
    NAT1, Arylamide Acetylase 1, AAC1, Arylamine N-Acetyltransferase 1, Acetyl-CoA:Arylamine N-Acetyltransferase
  • Bladder Cancer
    OMIM # 109800
  • Protoporphyria, Erythropoietic, 1
    OMIM # 177000
    EPP1, Protoporphyria, Erythropoietic, EPP, Erythrohepatic Protoporphyria, Heme Synthetase Deficiency, Ferrochelatase Deficiency
  • Ferrochelatase
    OMIM # 612386
    FECH, Heme synthase, Heme Synthetase, Iron Chelatase
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