ORPHA:2458
OBSOLETE: Mandibulofacial dysostosis-deafness-postaxial polydactyly syndrome
inactive · referred to ORPHA:364526Primary bone dysplasia
Synonyms: OBSOLETE: Opitz-Reynolds-Fitzgerald syndrome
- 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 Primary bone dysplasia
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Mandibulofacial dysostosis-deafness-postaxial polydactyly syndrome | OBSOLETE: Opitz-Reynolds-Fitzgerald syndrome |
| fr | OBSOLETE : Syndrome de dysostose mandibulo-faciale-surdité-polydactylie postaxiale | OBSOLETE : Syndrome d'Opitz-Reynolds-Fitzgerald |
| de | OBSOLET: Mandibulofaziale Dysostose-Schwerhörigkeit-Postaxiale Polydaktylie-Syndrom | OBSOLET: Opitz-Reynolds-Fitzgerald-Syndrom |
| es | OBSOLETO: Síndrome de disostosis mandibulofacial-sordera-polidactilia postaxial | OBSOLETO: Síndrome de Opitz-Reynolds-Fitzgerald |
| it | OBSOLETO: Sindrome disostosi mandibolofacciale-sordità -polidattilia postassiale | OBSOLETO: Sindrome di Opitz-Reynolds-Fitzgerald |
| nl | OBSOLEET: Mandibulofaciale dysostose - doofheid - postaxiale polydactylie-syndroom | OBSOLEET: Syndroom van Opitz-Reynolds-FitzGerald |
| pt | OBSOLETO: Síndrome de disostose mandibulo-facial-surdez-polidactilia pós-axial | OBSOLETO: Síndrome Opitz-Reynolds-Fitzgerald |
| pl | NIEAKTUALNE: Zespół dysostozy żuchwowo-twarzowej, głuchoty i polidaktylii zaosiowejlia pozaosiowa | NIEAKTUALNE: Zespół Opitza, Reynoldsa i FitzGeralda |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující mandibulofaciální dysostózu-hluchotu-postaxiální polydaktylii | = en |
| uk | ЗАСТАРІЛО: Синдром щелепно-лицевого дизостозу-глухоти-постаксіальної полідактилії | ЗАСТАРІЛО: Синдром Опітца-Рейнольдса-Фітцджеральда |
| zh | 弃用：下颌骨发育不全-耳聋-轴后性多指综合征 | Opitz-Reynolds-FitzGerald 综合征 |
| tr | Eski adı: Mandibulofasiyal dizostoz-sağırlık-postaksiyal polidaktili sendromu | Opitz-Reynolds-FitzGerald sendromu |
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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.
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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/2458
- This record as JSON: /data/d/2458.json