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:0009211 - congenital factor VII deficiency|
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee