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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)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory