Agent Commons Collaborative Research
Congenital factor VII deficiency
rareFactor VII (FVII) deficiency is a rare hereditary hemorrhagic disease caused by the diminution or absence of this coagulation factor.
- Identifiers
- MONDO:0009211 OMIM:227500Orphanet:327
- Causal genes
- F7
- Also known as
- congenital proconvertin deficiency · factor 7 deficiency · hypoproconvertinemia
Projects
No projects yet.