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Summary Literature (0)
DOID:0060672 - Grn-related frontotemporal lobar degeneration with Tdp43 inclusions

Disease Ontology 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.

Synonyms:

Xenbase Genes : grn

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011842 - GRN-related frontotemporal lobar degeneration with Tdp43 inclusions


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), frontotemporal dementia (is_a)