ORPHA:2716
OBSOLETE: Oculo-skeletal-renal syndrome
inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Oculo-skeletal-renal syndrome | |
| fr | OBSOLETE : Syndrome oculo-squeletto-rénal | |
| de | OBSOLET: Okulo-skeleto-renales Syndrom | |
| es | OBSOLETO: Síndrome óculo-esqueleto-renal | |
| it | OBSOLETO: Sindrome oculo-scheletro-renale | |
| nl | OBSOLEET: Oculo-skeletaal-renaal syndroom | |
| pt | OBSOLETO: Síndrome oculo-esquelético-renal | |
| pl | NIEAKTUALNE: Zespól oczno-szkieletowo-nerkowy | |
| cs | NEAKTUÁLNÍ: Okuloskeletorenální syndrom | |
| uk | ЗАСТАРІЛО: Окулоскелетнонирковий синдром | |
| zh | 弃用：眼-骨骼-肾综合征 | |
| tr | Eski adı: Okülo-iskelet-böbrek sendromu |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
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/2716
- This record as JSON: /data/d/2716.json