ORPHA:391479
OBSOLETE: Syndromic frontonasal dysplasia
inactive · referred to ORPHA:250Frontonasal dysplasia
Synonyms: OBSOLETE: Syndromic median cleft syndrome
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Frontonasal dysplasia
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Syndromic frontonasal dysplasia | OBSOLETE: Syndromic median cleft syndrome |
| fr | OBSOLETE : Dysplasie fronto-nasale syndromique | OBSOLETE : Syndrome de la fente faciale médiane, forme syndromique |
| de | OBSOLET: Dysplasie, fronto-nasale, syndromale Form | |
| es | OBSOLETO: Displasia frontonasal sindrómica | OBSOLETO: Síndrome de fisura media facial |
| it | OBSOLETO: Displasia frontonasale sindromica | OBSOLETO: Sindrome da schisi mediana sindromica |
| nl | OBSOLEET: Syndromale frontonasale dysplasie | OBSOLEET: Syndromaal mediane splijting-syndroom |
| pt | OBSOLETO: Displasia frontonasal sindromática | |
| pl | NIEAKTUALNE: Syndromiczna dysplazja czolowo-nosowa | NIEAKTUALNE: Syndromiczny zespół rozszczepu pośrodkowego |
| cs | NEAKTUÁLNÍ: Syndromická frontonazální dysplázie | = en |
| uk | ЗАСТАРІЛО: Синдромальна фронтоназальна дисплазія | ЗАСТАРІЛО: Синдром серединної розщілини |
| zh | 弃用：综合征性额鼻部发育不良 | 综合征性面部正中裂综合征 |
| tr | Eski adı: Sendromik frontonazal displazi | Sendromik medyan yarık 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/391479
- This record as JSON: /data/d/391479.json