D68Level 2

Other coagulation defects

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D680Von Willebrand disease

D681Hereditary factor XI deficiency

D682Hereditary deficiency of other clotting factors

D683Hemorrhagic disorder due to circulating anticoagulants

D684Acquired coagulation factor deficiency

D685Primary thrombophilia

D686Other thrombophilia

D688Other specified coagulation defects

D689Coagulation defect, unspecified

No cross-system equivalences mapped for this node.