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Ontology Browser

Term:
Congenital Dysfibrinogenemia (DOID:9003464)
Annotations: Rat: (3) Mouse: (3) Human: (3) Chinchilla: (3) Bonobo: (3) Dog: (3) Squirrel: (3) Pig: (3)
Parent Terms Term With Siblings Child Terms
Congenital Dysfibrinogenemia  
A hereditary, usually autosomal dominant disorder that affects the quality of circulating FIBRINOGEN. About half of patients are asymptomatic, and half have an increased tendency for bleeding, THROMBOSIS, or both. (MESH)
Congenital Hypodysfibrinogenemia  

Synonyms
Narrow Synonyms: DYSFIBRINOGENEMIA ;   congenital hypodysfibrinogenemia
Related Synonyms: FIBRINOGEN AARHUS 1 ;   FIBRINOGEN ASAHI ;   FIBRINOGEN BALTIMORE 4 ;   FIBRINOGEN BERGAMO 2 ;   FIBRINOGEN CARACAS 2 ;   FIBRINOGEN CARACAS II ;   FIBRINOGEN PETOSKEY
Primary IDs: MESH:C562727
Alternate IDs: OMIM:616004

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