Search Ontology:
Human Disease

Grn-related frontotemporal lobar degeneration with Tdp43 inclusions

Term ID
DOID:0060672
Synonyms
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. (2)
References
Ontology
Human Disease   ( DOID:0060672 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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