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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
OMIM:202400 - AFIBRINOGENEMIA, CONGENITAL |
MONDO:0008737 - congenital afibrinogenemia |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s):
autosomal recessive disease (is_a),
blood coagulation disease (is_a),
physical disorder (is_a)