3B15ICD-11 MMS 2026-01
Inherited coagulation factor deficiency without bleeding tendency
Description
A disease caused by a genetically inherited mutation leading to decreased levels of coagulation factor. This disease is characterised by decreased levels of coagulation factor without leading to increased haemorrhaging. Confirmation is by identification of decreased levels of coagulation factor in a blood sample.
Index terms
- Inherited coagulation factor deficiency without bleeding tendency
- Congenital prekallikrein deficiency
- Congenital high-molecular-weight kininogen deficiency
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- Hereditary factor XII deficiency
- Congenital Hageman factor deficiency
- Deficiency of factor XII
- Hageman defect
- Hageman deficiency
- Hageman factor defect
- Hageman factor deficiency
- congenital factor XII deficiency
- factor XII deficiency disease
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
Inherited coagulation factor deficiency without bleeding tendency – http://id.who.int/icd/entity/1795705470
Part of: 03: Diseases of the blood or blood-forming organs