ORPHA:138063
OBSOLETE: Syndrome associated with Pierre Robin syndrome
inactive · referred to ORPHA:138044Rare disease with Pierre Robin syndrome
Synonyms: OBSOLETE: Syndrome associated with Pierre Robin sequence
- 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 Rare disease with Pierre Robin syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Syndrome associated with Pierre Robin syndrome | OBSOLETE: Syndrome associated with Pierre Robin sequence |
| fr | OBSOLETE : Syndrome associé à un syndrome de Pierre Robin | OBSOLETE : Syndrome associé à une séquence de Pierre Robin |
| de | OBSOLET: Syndrom mit assoziierter Pierre-Robin-Sequenz | OBSOLET: Syndrom in Assoziation mit Pierre-Robin-Syndrom |
| es | OBSOLETO: Síndrome asociado al síndrome de Pierre Robin | OBSOLETO: Síndrome asociado a la secuencia de Pierre Robin |
| it | OBSOLETO: Sindrome associata alla sindrome di Pierre Robin | OBSOLETO: Sindrome associata alla sequenza di Pierre Robin |
| nl | OBSOLEET: Syndroom geassocieerd met syndroom van Pierre Robin | OBSOLEET: Syndroom geassocieerd met Pierre Robin sequentie |
| pt | OBSOLETO: Síndrome associado a sequência de Pierre Robin | |
| pl | NIEAKTUALNE: Zespól zwiazany z zespolem Pierre' a Robina | NIEAKTUALNE: Zespół związany z sekwencją Pierre' a Robina |
| cs | NEAKTUÁLNÍ: Syndrom spojený s Pierre Robinovým syndromem | = en |
| uk | ЗАСТАРІЛО: Синдром, повязаний із синдромом Пєра Робена | ЗАСТАРІЛО: Синдром, асоційований з послідовністю Пєра Робена |
| zh | 弃用：与Pierre Robin综合征相关的综合征 | Pierre-Robin序列征相关综合征 |
| tr | Eski adı: Pierre Robin sendromu -ilişkili sendrom | Pierre Robin dizisi ile seyreden sendrom |
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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/138063
- This record as JSON: /data/d/138063.json