ORPHA:141327
OBSOLETE: Orofaciodigital syndrome type 12
inactive · referred to ORPHA:140997Orofaciodigital syndrome
Synonyms: OBSOLETE: Moran-Barroso syndrome · OBSOLETE: OFD12 · OBSOLETE: Oral-facial-digital syndrome type 12
- 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 Orofaciodigital syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Orofaciodigital syndrome type 12 | OBSOLETE: Moran-Barroso syndrome · OBSOLETE: OFD12 · OBSOLETE: Oral-facial-digital syndrome type 12 |
| fr | OBSOLETE : Syndrome oro-facio-digital type 12 | OBSOLETE : OFD12 · OBSOLETE : Syndrome de Moran-Barroso |
| de | OBSOLET: Oro-fazio-digitales Syndrom Typ 12 | OBSOLET: Moran-Barroso-Syndrom · OBSOLET: OFD12 · OBSOLET: Oral-fazial-digitales Syndrom Typ 12 |
| es | OBSOLETO: Síndrome orofaciodigital tipo 12 | OBSOLETO: Síndrome oro-facio-digital tipo 12 · OBSOLETO: OFD12 · OBSOLETO: Síndrome de Moran-Barroso |
| it | OBSOLETO: Sindrome orofaciodigitale tipo 12 | OBSOLETO: OFD12 · OBSOLETO: Sindrome di Moran-Barroso · OBSOLETO: Sindrome oro-facio-digitale tipo 12 · OBSOLETO: Sindrome oro-facio-digitale, tipo 12 · OBSOLETE: Sindrome di Moran-Barroso |
| nl | OBSOLEET: Orofaciodigitaal syndroom type 12 | OBSOLEET: OFD12 · OBSOLEET: Oraal-faciaal-digitaal syndroom type 12 · OBSOLEET: Syndroom van Moran-Barroso |
| pt | OBSOLETO: Síndrome orofaciodigital tipo 12 | |
| pl | NIEAKTUALNE: Zespół ustno-twarzowo-palcowy typu 12 | NIEAKTUALNE: OFD12 |
| cs | NEAKTUÁLNÍ: Orofaciodigitální syndrom, typ 12 | NEAKTUÁLNÍ: OFD12 |
| uk | ЗАСТАРІЛО: Орофаціодигітальний синдром, тип 12 | ЗАСТАРІЛО: Синдром Морана-Баррозу · ЗАСТАРІЛО: OFD12 · ЗАСТАРІЛО: Орально-лицево-пальцевий синдром, тип 12 |
| zh | 口面指综合征12型 | 口-面-指综合征12型 |
| tr | Orofasiyodijital sendrom tip 12 | OFD12 · Moran-Barroso sendromu · Oral-fasiyal-dijital sendromu tip 12 |
Definition in:
2
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/141327
- This record as JSON: /data/d/141327.json