Disease-gene associations mined from literature

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