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congenital factor X deficiency

Disease Summary
Associated Targets (1)
Tclin

1


GARD Rare
Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0009212:  congenital factor X deficiency
GARD:0006404: 
NCIT:C98940: 
Orphanet:328: 
SCTID:37350004: