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Summary Literature (0)
DOID:2215 - factor VII deficiency

Disease Ontology Definition:A blood coagulation disease that is characterized by easy bleeding, has_symptom epistaxis, bleeding of the gums, menorrhagia, and occasionally hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation in the F7 gene, which encodes coagulation factor VII, an important factor in the clotting cascade.

Synonyms: Factor VII deficiency, Factor VII deficiency (disorder), deficiency, stable

Xenbase Genes : f7

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009211 - congenital factor VII deficiency

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)