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Disease Ontology Browser
factor VII deficiency (DOID:2215)
Alliance: disease page
Synonyms: deficiency, stable
Alt IDs: OMIM:227500, ICD10CM:D68.2, MESH:D005168, NCI:C131631, ORDO:327, UMLS_CUI:C0015503
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory