Prothrombin deficiency, congenital

Disease ID:793
Name:Prothrombin deficiency, congenital
Associated with:1 target
Synonyms
Congenital factor II deficiency | Prothrombin deficiency
Database Links
Disease Ontology: DOID:2235
OMIM: 613679
Orphanet: ORPHA325

Targets

coagulation factor II, thrombin

Ligands

No ligand related data available for Prothrombin deficiency, congenital