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Disease Ontology Browser
factor V deficiency (DOID:2216)
Alliance: disease page
Synonyms: deficiency, labile; Hereditary hypoproaccelerinaemia; Labile factor deficiency; Proaccelerin deficiency
Alt IDs: OMIM:227400, ICD10CM:D68.2, MESH:D005166, NCI:C98938, UMLS_CUI:C0015499

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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last database update
MGI 6.19
The Jackson Laboratory