congenital afibrinogenemia

Summary

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

In OMIM:

OMIM:202400 - AFIBRINOGENEMIA, CONGENITAL

OMIM:202400 - AFIBRINOGENEMIA, CONGENITAL

In Mondo Disease Ontology:

MONDO:0008737 - congenital afibrinogenemia

MONDO:0008737 - congenital afibrinogenemia

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: fgg, fga, fgb

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)