About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory