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

deficiency, stable

Cross References

Parent Terms

Child Terms

None

Sources of Associations

Associated Genes

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factor VII deficiency

factor VII deficiency

Associated Genes

Associated Alleles

Associated Models