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congenital factor XI deficiency

Disease Summary
Associated Targets (4)
Tchem

3

Tbio

1


GARD Rare
Mondo Description Congenital factor XI deficiency is an inherited bleeding disorder characterized by reduced levels and activity of factor XI (FXI) resulting in moderate bleeding symptoms, usually occurring after trauma or surgery.
Mondo Term and Equivalent IDs
MONDO:0012897:  congenital factor XI deficiency
COHD:437256: 
GARD:0009670: 
ICD9:286.2: 
MESH:D005173: 
NCIT:C84705: 
Orphanet:329: 
SCTID:49762007: 
UMLS:C0015523: