Immune thrombocytopenic purpura (Q39624): Difference between revisions
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Revision as of 05:06, 13 August 2026
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B64.10 |
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| English | Immune thrombocytopenic purpura |
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. |
