3B64.10ICD-11 MMS 2026-01
Immune thrombocytopenic purpura
Description
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.
Index terms
- Immune thrombocytopenic purpura
- Frank's essential thrombocytopenia
- ITP - [idiopathic thrombocytopenia purpura]
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- 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
Exclusions from above levels
JA43.3– Postpartum coagulation defects04– Diseases of the immune system05– Endocrine, nutritional or metabolic diseases
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18– Complications of pregnancy, childbirth or the puerperium19– Certain conditions originating in the perinatal period20– Congenital malformations, deformations or chromosomal abnormalities22– Injury, poisoning or certain other consequences of external causes- http://id.who.int/icd/entity/1000704511 – Human immunodeficiency virus disease
JB64.1– Other diseases of the blood or blood-forming organs or certain disorders involving the immune mechanism complicating pregnancy, childbirth or the puerperium
Foundation children elsewhere
3A20.5– Evans syndrome
Sibling codes
Foundation entity
Immune thrombocytopenic purpura – http://id.who.int/icd/entity/364346400
Part of: 3B64.1: Acquired thrombocytopenia › 3B64: Thrombocytopenia › 03: Diseases of the blood or blood-forming organs