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| Term | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions | ID (Ontology) | DOID:0060672 (Human Disease) |
| 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. | ||
| Also Known As | "frontotemporal dementia 2" | ||
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autosomal genetic disease |__autosomal dominant disease__ dementia | |__frontotemporal dementia_____| brain disease | |__frontotemporal dementia_____| GRN-related frontotemporal lobar degeneration with Tdp43 inclusions |
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autosomal dominant disease frontotemporal dementia |
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ICD10CM:G31.0 MIM:607485 |
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