About   Help   FAQ
Disease Ontology Browser
factor XII deficiency (DOID:2231)
Alliance: disease page
Synonyms: deficiency, Hageman; Factor XII deficiency disease; Hageman Factor deficiency
Alt IDs: OMIM:234000, MESH:D005175, NCI:C131740, ORDO:330, UMLS_CUI:C0015526
Definition: A blood coagulation disease that is characterized by prolonged PTT time without clinical symptoms, and has_material_basis_in a mutation in the F12 gene on chromosome 5q33.

Disease References using Mouse Models (1)

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
04/16/2024
MGI 6.23
The Jackson Laboratory