D65-D69
Coagulation defects, purpura and other haemorrhagic conditions
D65
Primary diagnosis candidate
Disseminated intravascular coagulation [defibrination syndrome]
D66
Primary diagnosis candidate
Hereditary factor VIII deficiency
D67
Primary diagnosis candidate
Hereditary factor IX deficiency
D68
Other coagulation defects
D68.0
Primary diagnosis candidate
Von Willebrand disease
D68.1
Primary diagnosis candidate
Hereditary factor XI deficiency
D68.2
Primary diagnosis candidate
Hereditary deficiency of other clotting factors
D68.3
Primary diagnosis candidate
Haemorrhagic disorder due to circulating anticoagulants
D68.4
Primary diagnosis candidate
Acquired coagulation factor deficiency
D68.5
Primary diagnosis candidate
Primary thrombophilia
D68.6
Primary diagnosis candidate
Other thrombophilia
D68.8
Primary diagnosis candidate
Other specified coagulation defects
D68.9
Primary diagnosis candidate
Coagulation defect, unspecified
D69
Purpura and other haemorrhagic conditions
D69.0
Primary diagnosis candidate
Allergic purpura
D69.1
Primary diagnosis candidate
Qualitative platelet defects
D69.2
Primary diagnosis candidate
Other nonthrombocytope nic purpura
D69.3
Primary diagnosis candidate
Idiopathic thrombocytopenic purpura
D69.4
Primary diagnosis candidate
Other primary thrombocytopenia
D69.5
Primary diagnosis candidate
Secondary thrombocytopenia
D69.6
Primary diagnosis candidate
Thrombocytopenia, unspecified
D69.8
Primary diagnosis candidate
Other specified haemorrhagic conditions
D69.9
Primary diagnosis candidate
Haemorrhagic condition, unspecified
