Thrombophilia due to protein C deficiency, autosomal dominant

Disease ID:916
Name:Thrombophilia due to protein C deficiency, autosomal dominant
Associated with:1 target
Synonyms
Hereditary thrombophilia due to congenital protein C deficiency | Thrombophilia
Database Links
Disease Ontology: DOID:2452
OMIM: 176860
Orphanet: ORPHA745

Targets

protein C, inactivator of coagulation factors Va and VIIIa

Ligands

No ligand related data available for Thrombophilia due to protein C deficiency, autosomal dominant