ORPHA:183763
Rare genetic syndromic intellectual disability
- 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 | Rare genetic syndromic intellectual disability | |
| fr | Déficience intellectuelle syndromique rare d'origine génétique | |
| de | Seltene syndromale Intelligenzminderung, genetisch bedingte | |
| es | Discapacidad intelectual rara genética sindrómica | |
| it | Disabilità intellettiva sindromica di origine genetica rara | |
| nl | Zeldzame genetische syndromale intellectuele achterstand | |
| pt | Perturbação do desenvolvimento intelectual sindromática genética rara | |
| pl | Rzadka niepełnosprawność intelektualna uwarunkowana genetycznie z zaburzeniem rozwoju | |
| cs | Vzácné dědičné syndromické mentální retardace | |
| uk | Рідкісний генетично обумовлений синдром інтелектуальної недостатності | |
| zh | 罕见遗传性综合征性智力障碍 | |
| tr | Nadir genetik sendromik zihinsel yetersizlik |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15983 | E | validated | |
| UMLS | C5680525 | 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:183757Rare genetic intellectual disability
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/183763
- This record as JSON: /data/d/183763.json