OMIM Phenotype&GeneSymbol  

  Chapter.3   Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
  D65-D69   Coagulation defects, purpura and other haemorrhagic conditions
    D68   Other coagulation defects ( Search )
    • D680   Von Willebrand disease ( Search )
    • D681   Hereditary factor XI deficiency ( Search )
    • D682   Hereditary deficiency of other clotting factors ( Search )
    • D683   Haemorrhagic disorder due to circulating anticoagulants ( Search )
    • D684   Acquired coagulation factor deficiency ( Search )
    • D688   Other specified coagulation defects ( Search )
    • D689   "Coagulation defect, unspecified" ( Search )
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