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CTGA Database Listing
Arab Genomic Studies
Records found: 2565 Sort by:
  • Thrombocythemia 3
    OMIM # 614521
    THCYT3, Thrombocytosis 3
  • Janus Kinase 2
    OMIM # 147796
    JAK2 , JAK2/ETV6 Fusion Gene
  • Parkinson Disease
    OMIM # 168600
    PD, PARK
  • Paramyotonia Congenita of Von Eulenburg
    OMIM # 168300
    PMC, Paralysis Periodica Paramyotonica, Paralysis Periodica Paramyotonia, Paramyotonia Congenita without Cold Paralysis
  • Pancreas, Annular
    OMIM # 167750
  • Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant
    OMIM # 167100
    PHO, Autosomal Dominant, Pachydermoperiostosis, Autosomal Dominant, PDP, Autosomal Dominant
  • Ovarian Cancer
    OMIM # 167000
    Ovarian Cancer, Epithelial, Suppressor of Tumorigenicity 8, ST8, Ovarian Cancer, Familial, Ovarian Tumor, Peritoneal Ovarian Carcinomatosis, Neonatal Ovarian Cyst, Fetal Ovarian Cyst
  • Vohwinkel Syndrome, Variant Form
    OMIM # 604117
    Vohwinkel Syndrome with Ichthyosis , Mutilating Keratoderma with Ichthyosis , Loricrin Keratoderma
  • Loricrin
    OMIM # 152445
    LOR , Epidermal Differentiation Complex , EDC
  • Protein Kinase, Lysine-Deficient 1
    OMIM # 605232
    WNK1 , Prostrate-Derived Sterile 20-Like Kinase , PSK, PRKWNK1, KDP, KIAA0344
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