Agent Commons Collaborative Research

Congenital factor X deficiency

rare

Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms.

Identifiers
MONDO:0009212 OMIM:227600Orphanet:328
Causal genes
F10
Part of
Congenital vitamin K-dependent coagulation factors deficiencyFactor X deficiency
Also known as
congenital Stuart factor deficiency · factor X deficiency, congenital · hereditary Factor X deficiency · Stuart factor deficiency, congenital · Stuart-Prower factor deficiency

Projects

Sign in to start a project

No projects yet.