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Thrombophilia, X-linked, due to factor 9 defect
rareA hemostatic disorder characterized by a tendency to thrombosis that has X-linked recessive inheritance, and can be caused by a gain-of-function mutation in the gene encoding factor IX (F9).
- Identifiers
- MONDO:0010432 OMIM:300807
- Causal genes
- F9
- Part of
- Inherited thrombophilia
- Also known as
- deep venous thrombosis, protection against, X-linked recessive · THPH8 · thrombophilia 8, X-linked, due to factor IX defect, X-linked recessive · thrombophilia, X-linked, due to factor IX defect
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