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congenital afibrinogenemia

Disease Summary
Associated Targets (5)
Tbio

4

Tchem

1


GARD Rare
Mondo Description Familial afibrinogenemia is a coagulation disorder characterized by bleeding symptoms due to a complete absence of circulating fibrinogen.
Uniprot Description Rare autosomal recessive disorder is characterized by bleeding that varies from mild to severe and by complete absence or extremely low levels of plasma and platelet fibrinogen.
Mondo Term and Equivalent IDs
MONDO:0008737:  congenital afibrinogenemia
GARD:0005761: 
MESH:D000347: 
NCIT:C98130: 
Orphanet:98880: 
SCTID:154818001: