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Summary Literature (0)
DOID:2236 - congenital afibrinogenemia


Disease Ontology Definition: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: Factor I deficiency, Fibrinogen deficiency

Xenbase Genes : fgg, fga, fgb

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008737 - congenital afibrinogenemia

OMIM:
OMIM:202400 - AFIBRINOGENEMIA, CONGENITAL

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), blood coagulation disease (is_a), physical disorder (is_a)