ORPHA:98549
Rare cerebrovascular 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare cerebrovascular dementia | |
| fr | Démence cérébrovasculaire rare | |
| de | Seltene zerebrovaskuläre Demenz | |
| es | Demencia cerebrovascular rara | |
| it | Demenza cerebrovascolare | |
| nl | Zeldzame cerebrovasculaire dementie | |
| pt | Demência cerebrovascular | |
| pl | Demencja mózgowo-naczyniowa | |
| cs | Cerebrovaskulární demence | |
| uk | Рідкісна цереброваскулярна деменція | |
| zh | 罕见脑血管性伴痴呆 | |
| tr | Nadir serebrovasküler demans |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681729 | 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 (2):
- ORPHA:158124Genetic dementia
rare genetic diseases - ORPHA:89043Rare dementia
rare neurological diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:1249OBSOLETE: Binswanger disease referred to · inactive
- ORPHA:371439OBSOLETE: Genetic cerebrovascular dementia referred to · inactive
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98549
- This record as JSON: /data/d/98549.json