3B64.14ICD-11 MMS 2026-01
Thrombotic thrombocytopenic purpura
Description
This condition is idiopathic. This condition is characterised by abnormality of blood coagulation causing extensive microscopic clots to form in the small blood vessels throughout the body resulting in low platelet count. This condition may present with seizures, hemiplegia, paresthesias, visual disturbance, and aphasia or anaemia. Confirmation is by identification of thromboses.
Index terms
- Thrombotic thrombocytopenic purpura
- Moschcowitz disease
- Moschcowitz syndrome
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- TTP - [thrombotic thrombocytopenic purpura]
- Acquired thrombotic thrombocytopenic purpura due to anti-ADAMTS 13 antibodies
- Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency
- Upshaw-Schulman syndrome
- congenital thrombocytopaenic purpura
- Glomerular disorders in thrombotic thrombocytopenic purpura
- Thrombotic 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
Sibling codes
Foundation entity
Thrombotic thrombocytopenic purpura – http://id.who.int/icd/entity/1708277768
Part of: 3B64.1: Acquired thrombocytopenia › 3B64: Thrombocytopenia › 03: Diseases of the blood or blood-forming organs