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CTGA Database Listing
Arab Genomic Studies
Records found: 2741 Sort by:
  • 5,10-@Methylenetetrahydrofolate Reductase
    OMIM # 607093
    MTHFR
  • Internal Carotid Artery, Spontaneous Dissection of
    OMIM # 147820
  • Low Density Lipoprotein Receptor
    OMIM # 606945
    LDLR
  • Natriuretic Peptide Receptor 2
    OMIM # 108961
    NPR2; , Guanylate Cyclase B; , GCB; , GUC2B; , GUCY2B; , Atrial Natriuretic Peptide Receptor, Type B;, ANPRB; , Atrionatriuretic Peptide Receptor, Type B; , NPRB; , ANPB Receptor,
  • Acromesomelic Dysplasia, Maroteaux Type
    OMIM # 602875
    AMDM, St. Helena Dysplasia
  • 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
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