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Disease Ontology Browser
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions (DOID:0060672)
Alliance: disease page
Alt IDs: OMIM:607485, ICD10CM:G31.0
Definition: A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31.

Disease References using Mouse Models (11)

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 6.17
The Jackson Laboratory