3B14.1 Hereditary factor X deficiency

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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
• Stuart-Prower factor deficiency
• Deficiency of factor X
• congenital factor x deficiency
• Stuart deficiency disease
• Stuart Prower deficiency
• Stuart-Prower disease

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