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 ...