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CTGA Database Listing
Arab Genomic Studies
Records found: 2565 Sort by:
  • WD Repeat-Containing Protein 73
    OMIM # 616144
    WDR73, HSPC264,
  • Factor VII Deficiency
    OMIM # 227500
    F7 Deficiency, Hypoproconvertinemia,
  • Coagulation Factor VII
    OMIM # 613878
    F7 , Factor VII
  • Myeloma, Multiple
    OMIM # 254500
    Amyloidosis, Systemic , AL, AL Amyloidosis
  • 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
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