Purpura and other hemorrhagic conditions
Notes: Allergic vasculitis ; Nonthrombocytopenic hemorrhagic purpura ; Nonthrombocytopenic idiopathic purpura ; Purpura anaphylactoid ; Purpura Henoch(-Schönlein) ; Purpura rheumatica ; Vascular purpura ; Bernard-Soulier [giant platelet] syndrome ; Glanzmann’s disease ; Grey platelet syndrome ; Thromboasthenia (hemorrhagic) (hereditary) ; Thrombocytopathy ; Purpura NOS ; Purpura simplex ; Senile purpura ; Hemorrhagic (thrombocytopenic) purpura ; Idiopathic thrombocytopenic purpura ; Tidal platelet dysgenesis ; Congenital thrombocytopenia ; Hereditary thrombocytopenia ; Megakaryocytic hypoplasia ; Primary thrombocytopenia NOS ; Posttransfusion purpura from whole blood (fresh) or blood products ; PTP ; Capillary fragility (hereditary) ; Vascular pseudohemophilia ; benign hypergammaglobulinemic purpura (D89.0) ; cryoglobulinemic purpura (D89.1) ; essential (hemorrhagic) thrombocythemia (D47.3) ; hemorrhagic thrombocythemia (D47.3) ; purpura fulminans (D65) ; thrombotic thrombocytopenic purpura (M31.19) ; Waldenström hypergammaglobulinemic purpura (D89.0) ; thrombocytopenic hemorrhagic purpura (D69.3) ; hemolytic-uremic syndrome (D59.3-) ; transient neonatal thrombocytopenia (P61.0) ; Wiskott-Aldrich syndrome (D82.0) ; heparin induced thrombocytopenia (HIT) (D75.82-) ; transient thrombocytopenia of newborn (P61.0) ; von Willebrand disease (D68.0-) ; congential or hereditary disorder, such as: ; thrombocytopenia with absent radius (TAR syndrome) (Q87.2)