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Disease Ontology Browser
frontotemporal dementia 1 (DOID:0051060)
Alliance: disease page
Alt IDs: OMIM:600274, MESH:C563003
Definition: A frontotemporal dementia that has_material_basis_in heterozygous mutation in the MAPT gene, which encodes microtubule-associated protein tau, on chromosome 17q21.

Disease References using Mouse Models (3)
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
05/19/2026
MGI 6.24 		The Jackson Laboratory