Human genes for factor VII deficiency
Factor VII deficiency [DOID:2215]
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, DOID:2215, factor VII deficiencies, deficiency, stable, deficiency stable ...
Linkouts: OMIM