Grn-Related Frontotemporal Lobar Degeneration With Tdp43 Inclusions
Disease ID: disease_node_18035
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| Dbxref | ICD10CM:G31.0, MIM:607485 |
|---|---|
| Subclassof | DOID_0050736, DOID_9255 |
| Data Source | DOID |
| Doid Label | Grn-related frontotemporal lobar degeneration with Tdp43 inclusions |
| Doid 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. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_18035 |
| Doid Id | DOID_0060672 |
| Label | Grn-Related Frontotemporal Lobar Degeneration With Tdp43 Inclusions |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)