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Congenital factor XI deficiency
rareCongenital factor XI deficiency is an inherited bleeding disorder characterized by reduced levels and activity of factor XI (FXI) resulting in moderate bleeding symptoms, usually occurring after trauma or surgery.
- Identifiers
- MONDO:0012897 OMIM:612416Orphanet:329
- Causal genes
- F11
- Part of
- Autosomal genetic diseaseCongenital hematological disorderFactor XI deficiencyHemorrhagic diseaseInherited blood coagulation disorder
- Also known as
- factor XI deficiency, autosomal dominant · factor XI deficiency, autosomal recessive · haemophilia C · hemophilia C · hereditary Factor XI deficiency
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