3B64.10 Immune thrombocytopenic purpura

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2026-01

Immune thrombocytopenic purpura (or immune thrombocytopenia; ITP) is an autoimmune coagulation disorder characterised by isolated thrombocytopenia (a platelet count <100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia.

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• Evans syndrome  (3A20.5)

synonyms

• Immune thrombocytopenic purpura
• Frank's essential thrombocytopenia
• ITP - [idiopathic thrombocytopenia purpura]
• Werlhof disease
• autoimmune thrombocytopenic purpura
• essential thrombocytopenia
• haemorrhagic purpura
• idiopathic purpura
• idiopathic thrombocytopenia
• idiopathic thrombocytopenia purpura
• idiopathic thrombocytopenic purpura
• primary autoimmune thrombocytopenic purpura
• purpura haemorrhagica
• Immune thrombocytopenic purpura specified as refractory

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