ORPHA:139477
Al-Gazali-Dattani syndrome
inactive · moved to ORPHA:324737SRD5A3-CDG
- 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 SRD5A3-CDG
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Al-Gazali-Dattani syndrome | |
| fr | Syndrome d'Al-Gazali-Dattani | |
| de | Al-Gazali-Dattani-Syndrom | |
| es | Síndrome de Al-Gazali-Dattani | |
| it | Sindrome di Al-Gazali-Dattani | |
| nl | Syndroom van Al-Gazali-Dattani | CDG1Q |
| pt | Síndrome de Al-Gazali-Dattani | |
| pl | Zespół Al-Gazaliego i Dattaniego | |
| cs | Al-Gazaliové-Dattaniho syndrom | Al-Gazali-Dattaniho syndrom |
| uk | Синдром Аль-Газалі-Даттані | |
| zh | Al-Gazali-Dattani综合征 | |
| tr | Al-Gazali-Dattani 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/139477
- This record as JSON: /data/d/139477.json