Grn-related frontotemporal lobar degeneration with Tdp43 inclusions
Information
- Disease name
- Grn-related frontotemporal lobar degeneration with Tdp43 inclusions
- Disease ID
- DOID:0060672
- 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." [url:https\://www.ncbi.nlm.nih.gov/pubmed/16862116, url:https\://www.ncbi.nlm.nih.gov/pubmed/16983677]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:9255
- Cross Reference ID (Disease Ontology)
- ICD10CM:G31.0
- Cross Reference ID (Disease Ontology)
- MIM:607485