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congenital prothrombin deficiency

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms.
Uniprot Description A very rare blood coagulation disorder characterized by mucocutaneous bleeding symptoms. The severity of the bleeding manifestations correlates with blood factor II levels.
Mondo Term and Equivalent IDs
MONDO:0013361:  congenital prothrombin deficiency
GARD:0002235: 
MESH:D007020: 
NCIT:C131737: 
Orphanet:325: 
SCTID:73975000: 
UMLS:C0020640: