ORPHA:79458
Oley syndrome
inactive · moved to ORPHA:113Bazex-Dupré-Christol syndrome
Synonyms: Congenital hypotrichosis-milia 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 Bazex-Dupré-Christol syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Oley syndrome | Congenital hypotrichosis-milia syndrome |
| fr | Syndrome d'Oley | Syndrome d'hypotrichose congénitale-milia |
| de | Oley-Syndrom | Kongenitale Hypotrichose - Milien |
| es | Síndrome de Oley | Hipotricosis congénita-milia |
| it | Sindrome di Oley | Ipotricosi congenita - milia |
| nl | Syndroom van Oley | Congenitale hypotrichose - milia-syndroom |
| pt | Síndrome Oley | Hipotricose-congénita-mília |
| pl | Zespół Oley'a | Wrodzona hipotrichoza - prosaki |
| cs | Oleyové syndrom | Syndrom zahrnující vrozenou hypotrichózu a milia |
| uk | Синдром Олі | Синдром вродженого гіпотрихозу-мілії |
| zh | Oley综合征 | 先天性少毛-粟粒疹综合征 |
| tr | Oley sendromu | Doğumsal hipotrikoz-milia sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79458
- This record as JSON: /data/d/79458.json