ORPHA:3118
Rudiger syndrome
inactive · moved to ORPHA:798Schinzel-Giedion syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Schinzel-Giedion syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rudiger syndrome | |
| fr | Syndrome de Rudiger | |
| de | Rüdiger-Syndrom | |
| es | Síndrome de Rudiger | |
| it | Sindrome di Rudiger | |
| nl | Syndroom van Rudiger | |
| pt | Síndrome Rudiger | |
| pl | Zespół Rudigera | |
| cs | Rudigerův syndrom | |
| uk | Синдром Рудігера | |
| zh | Rudiger综合征 | |
| tr | Rudiger sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 268650 | E | validated | |
| UMLS | C3502049 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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/3118
- This record as JSON: /data/d/3118.json