ORPHA:1530
OBSOLETE: Craniosynostosis-cataract syndrome
inactive · referred to ORPHA:139393Syndromic craniosynostosis
- 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 Syndromic craniosynostosis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Craniosynostosis-cataract syndrome | |
| fr | OBSOLETE : Syndrome de craniosynostose-cataracte | |
| de | OBSOLET: Kraniosynostose-Katarakt-Syndrom | |
| es | OBSOLETO: Síndrome de craneosinostosis-catarata | |
| it | OBSOLETO: Craniostenosi - cataratta | |
| nl | OBSOLEET: Craniosynostose - cataract-syndroom | |
| pt | OBSOLETO: Síndrome de craniostenose-catarata | |
| pl | NIEAKTUALNE: zespół przedwczesnego zarastania szwów czaszkowych z zaćmą | |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující kraniosynostózu a kataraktu | |
| uk | ЗАСТАРІЛО: Синдром краніосиностозу-катаракти | |
| zh | 弃用：颅缝早闭-白内障综合征 | |
| tr | Eski adı: Kraniosinostoz-katarakt 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/1530
- This record as JSON: /data/d/1530.json