ORPHA:2506
Michels syndrome
inactive · moved to ORPHA:2938433MC syndrome
Synonyms: 3MC1 syndrome · Oculopalatoskeletal syndrome
- 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 3MC syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Michels syndrome | 3MC1 syndrome · Oculopalatoskeletal syndrome |
| fr | Syndrome de Michels | Syndrome 3MC1 · Syndrome oculo-palato-squelettique |
| de | Michels-Syndrom | 3MC1-Syndrom · Okulo-palato-skelettales Syndrom |
| es | Síndrome de Michels | Síndrome 3MC1 · Síndrome óculo-palato-esquelético |
| it | Sindrome di Michels | Sindrome 3MC1 · Sindrome oculo-palato-scheletrica |
| nl | Syndroom van Michels | 3MC1-syndroom · Oculopalatoskeletaal syndroom |
| pt | Síndrome Michels | Síndrome oculo-palato-esquelético |
| pl | Zespół Michelsa | Zespół 3MC1 · Zespół oczno-podniebienno-szkieletowy |
| cs | Michelsové syndrom | 3MC1 syndrom · Okulopalatoskeletální syndrom |
| uk | Синдром Міхельса | Синдром 3MC1 · Окулопалатоскелетний синдром |
| zh | Michels综合征 | 眼-腭-骨综合征 |
| tr | Michels sendromu | 3MC1 sendromu · Okülopalatoskeletal sendrom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 257920 | E | validated | |
| UMLS | C0796059 | 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/2506
- This record as JSON: /data/d/2506.json