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DO Term : Grn-related frontotemporal lobar degeneration with Tdp43 inclusions [DOID:0060672] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • OMIM:607485,
  • ICD10CM:G31.0,
  • 607485
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Disease

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Diseases --> Mouse genes

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents