3B22ICD-11 MMS 2026-01
Acquired haemophilia
Description
Acquired haemophilia is a rare haemorrhagic disease caused by production of anti-factor VIII antibodies and is sometimes associated with other autoimmune disorders, cancers, lymphoproliferative syndromes and multiple transfusions during the postpartum period.
Index terms
- Acquired haemophilia
- Autoimmune coagulation factor deficiency
- nonfamilial haemophilia
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- Acquired haemophilia A
- Acquired haemophilia B
- Acquired factor XIII deficiency
Exclusions from above levels
KA8F.0– vitamin K deficiency of newbornJA43.3– Postpartum coagulation defects04– Diseases of the immune system
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05– Endocrine, nutritional or metabolic diseases18– 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
Acquired haemophilia – http://id.who.int/icd/entity/1559879199
Allowed postcoordination axes
Part of: 03: Diseases of the blood or blood-forming organs