3B14.0 Hereditary deficiency of factor I

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

Congenital deficiencies of fibrinogen are coagulation disorders characterised by bleeding symptoms ranging from mild to severe resulting from reduced quantity and/or quality of circulating fibrinogen. Afibrinogenaemia (complete absence of fibrinogen) and hypofibrinogenaemia (reduced plasma fibrinogen concentration) correspond to quantitative anomalies of fibrinogen while dysfibrinogenaemia corresponds to a functional anomaly of fibrinogen. Hypo- and dysfibrinogenaemia may be frequently combined (hypodysfibrinogenaemia).

synonyms

• Hereditary deficiency of factor I
• Deficiency of factor 1
• Hereditary fibrinogen deficiency
• Deficiency of fibrinogen
• congenital fibrinogenopenia
• Hereditary afibrinogenaemia
• Congenital afibrinogenaemia
• Hereditary dysfibrinogenaemia
• congenital dysfibrinogenaemia
• dysfibrinogenaemia NOS
• Hereditary hypofibrinogenaemia
• congenital hypofibrinogenaemia
• Hereditary hypodysfibrinogenaemia

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