ORPHA:374
Goldenhar syndrome
inactive · moved to ORPHA:141132Craniofacial microsomia
Synonyms: Facioauriculovertebral sequence
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Oculo-auriculo-vertebral spectrum
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Goldenhar syndrome | Facioauriculovertebral sequence |
| fr | Syndrome de Goldenhar | Séquence facioauriculovertébrale |
| de | Goldenhar-Syndrom | |
| es | Síndrome de Goldenhar | Secuencia facio-aurículo-vertebral |
| it | Sindrome di Goldenhar | Displasia OAV · Displasia facio-auricolo-vertebrale · Displasia oculo-auricolo-vertebrale · Microsomia craniofacciale · OAVS · Sindrome oculo-auricolo-vertebrale · Spettro allargato della microsomia emifacciale · Spettro oculo-auricolo-vertebrale |
| nl | Syndroom van Goldenhar | Facioauriculovertebrale sequentie |
| pt | Síndrome Goldenhar | Displasia óculo-auriculo-vertebral · Microssomia hemifacial |
| pl | Zespół Goldenhara | Dysplazja OAV · Dysplazja oczno-uszno-kręgowa/kręgosłupowa · Dysplazja twarzowo-uszno-kręgowa/kręgosłupowa · OAVS · Rozszerzone spektrum mikrosomii połowy twarzy · Spektrum oczno-uszno-kręgowe/kręgosłupowe · Zespół oczno-uszno-kręgowy/kręgosłupowy |
| cs | Goldenharův syndrom | Facioaurikulovertebrální sekvence · OAV · OAVS · Okuloaurikulovertebrální dysplázie · Okuloaurikulovertebrální syndrom |
| uk | Синдром Гольденхара | Фаціоаурикуловертебральна послідовність |
| zh | Goldenhar综合征 | 面-耳-脊椎序列征 |
| tr | Goldenhar sendromu | Fasiyoaurikulovertebral dizi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MeSH | D006053 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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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/374
- This record as JSON: /data/d/374.json