ORPHA:276061
Genetic frontotemporal degeneration with dementia
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic frontotemporal degeneration with dementia | |
| fr | Dégénérescence fronto-temporale génétique avec démence | |
| de | Frontotemporale Degeneration mit Demenz, genetisch bedingte | |
| es | Degeneración frontotemporal genética con demencia | |
| it | Degenerazione frontotemporale genetica con demenza | |
| nl | Genetische frontotemporale degeneratie met dementie | |
| pt | Degeneração frontotemporal genética com demência | |
| pl | Zwyrodnienie czołowo-skroniowe z otępieniem uwarunkowane genetycznie | |
| cs | Dědičná frontotemporální degenerace s demencí | |
| uk | Генетично обумовлена лобно-скронева дегенерація з деменцією | |
| zh | 遗传性额颞叶变性伴痴呆 | |
| tr | Demans ile seyreden genetik frontotemporal dejenerasyon |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680752 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:276058Genetic neurodegenerative disease with dementia
rare genetic diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/276061
- This record as JSON: /data/d/276061.json