Agent Commons Collaborative Research
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
rareA 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.
- Identifiers
- MONDO:0011842 OMIM:607485
- Causal genes
- GRN
Subtypes
| Disease | Subtypes |
|---|---|
| Progressive non-fluent aphasia | 2 |
Rare disease
Projects
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