ORPHA:141136
Otomandibular syndrome
inactive · moved to ORPHA:141132Craniofacial microsomia
Synonyms: First branchial arch syndrome · Hemifacial microsomia · Laterofacial microsomia · Otomandibular dysostosis
- 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
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Otomandibular syndrome | First branchial arch syndrome · Hemifacial microsomia · Laterofacial microsomia · Otomandibular dysostosis |
| fr | Syndrome otomandibulaire | Dysostose oto-mandibulaire · Microsomie hémifaciale · Microsomie latéro-faciale · Syndrome du premier arc branchial |
| de | Mikrosomie, hemifaziale | Dysostose, otomandibuläre · Erster Kiemenbogen-Syndrom · Mikrosomie, laterofaziale · Otomandibuläres Syndrom |
| es | Síndrome otomandibular | Disostosis otomandibular · Microsomía hemifacial · Microsomía laterofacial · Síndrome del primer arco branquial |
| it | Microsomia emifacciale | |
| nl | Hemifaciale microsomie | Eerste kieuwboogsyndroom · Laterofaciale microsomie · Otomandibulair syndroom · Otomandibulaire dysostose |
| pt | Microssomia hemifacial | |
| pl | Połowicza mikrosomia twarzy | Dyzostoza uszno-żuchwowa · Mikrosomia bocznej części twarzy · Zespół pierwszego łuku skrzelowego · Zespół uszno-żuchwowy |
| cs | Hemifaciální mikrosomie | Syndrom prvního branchiálního oblouku · Laterální mikrosomie · Otomandibulární dysostóza · Otomandibulární syndrom |
| uk | Отомандибулярний синдром | Синдром першої гілки дуги · Геміфаціальна мікросомія · Латерофаціальна мікросомія · Отомандибулярний дизостоз |
| zh | 耳下颌骨综合征 | 第一鳃弓综合征 |
| tr | Otomandibular sendrom | Hemifasiyal mikrozomi · Laterofasiyal mikrozomi · Otomandibular dizostoz · İlk branşiyal ark sendromu |
2
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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/141136
- This record as JSON: /data/d/141136.json