ORPHA:1773
Sacrococcygeal dysgenesis association
inactive · moved to ORPHA:3027Caudal regression 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 Caudal regression syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Sacrococcygeal dysgenesis association | |
| fr | Dysgénésie sacro-coccygienne | |
| de | Dysgenesie, sakrokokzygeale | |
| es | Disgenesia sacrococcígea | |
| it | Disgenesia sacro-coccigea | |
| nl | Sacrococcygeale dysgenesie-associatie | |
| pt | Disgenesia sacrococcígea | |
| pl | Asocjacja dysgenezji krzyżowo-guzicznej | |
| cs | Sakrokokcygeální dysgeneze | |
| uk | Асоціація крижово-куприкової дисгенезії | |
| zh | 骶尾骨联合发育不全 | |
| tr | Sakrokoksigeal disgenezi ilişkisi |
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/1773
- This record as JSON: /data/d/1773.json