3B14.1 Hereditary factor X deficiency
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2026-01
Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterised by mild to severe bleeding symptoms.
synonyms
- Hereditary factor X deficiency
- Congenital Stuart factor deficiency
- Deficiency of factor X
- Stuart Prower deficiency
- Stuart deficiency disease
- Stuart-Prower disease
- Stuart-Prower factor deficiency
- congenital factor x deficiency
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