DISEASES

Disease-gene associations mined from literature

Human genes for congenital afibrinogenemia

Congenital afibrinogenemia [DOID:2236]

A blood coagulation disease that is characterized by an impaired blood clotting resulting from a lack deficiency of a the fibrinogen protein (coagulation factor I).

Synonyms:  congenital afibrinogenemia,  congenital afibrinogenemias,  DOID:2236,  Factor I deficiency,  Fibrinogen deficiency ...

Linkouts:  OMIM #1 #2