» Medical & Health » Diseases » D50-D89. Diseases of the blood & immune mechanism » D65-D69. Coagulation defects, purpura and other haemorrhagic conditions » D69. Purpura and other haemorrhagic conditions
|
Excludes: benign hypergammaglobulinaemic purpura ( D89.0 )
cryoglobulinaemic purpura ( D89.1 )
essential (haemorrhagic) thrombocythaemia ( D47.3 )
purpura fulminans ( D65 )
thrombotic thrombocytopenic purpura ( M31.1 )
D69.0
Allergic purpura
Purpura:
· anaphylactoid
· Henoch(-Schönlein)
· nonthrombocytopenic:
· haemorrhagic
· idiopathic
· vascular
Vasculitis, allergic
D69.1
Qualitative platelet defects
Bernard-Soulier [giant platelet] syndrome
Glanzmann's disease
Grey platelet syndrome
Thromboasthenia (haemorrhagic)(hereditary)
Thrombocytopathy
Excludes: von Willebrand's disease ( D68.0 )
D69.2
Other nonthrombocytopenic purpura
Purpura:
· NOS
· senile
· simplex
D69.3
Idiopathic thrombocytopenic purpura
Evans' syndrome
D69.4
Other primary thrombocytopenia
Excludes: thrombocytopenia with absent radius ( Q87.2 )
transient neonatal thrombocytopenia ( P61.0 )
Wiskott-Aldrich syndrome ( D82.0 )
D69.5
Secondary thrombocytopenia
Use additional external cause code (Chapter XX), if desired, to identify cause.
D69.6
Thrombocytopenia, unspecified
D69.8
Other specified haemorrhagic conditions
Capillary fragility (hereditary)
Vascular pseudohaemophilia
D69.9
Haemorrhagic condition, unspecified
Write Something Under This Category
|