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Congenital prothrombin deficiency
rareCongenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms.
- Identifiers
- MONDO:0013361 OMIM:613679Orphanet:325
- Causal genes
- F2
- Part of
- Autosomal recessive diseaseCongenital vitamin K-dependent coagulation factors deficiencyProthrombin deficiency
- Also known as
- Dysprothrombinemia · hereditary prothrombin deficiency
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