ORPHA:2507
OBSOLETE: Mickleson syndrome
inactive · referred to ORPHA:364526Primary bone dysplasia
- 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
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Mickleson syndrome | |
| fr | OBSOLETE : Syndrome de Mickleson | |
| de | OBSOLET: Mickleson-Syndrom | |
| es | OBSOLETO: Síndrome de Mickleson | |
| it | OBSOLETO: Sindrome di Mickleson | |
| nl | OBSOLEET: Syndroom van Mickleson | |
| pt | OBSOLETO: Síndrome Mickleson | |
| pl | NIEAKTUALNE: Zespól Micklesona | |
| cs | NEAKTUÁLNÍ: Micklesonův syndrome | |
| uk | ЗАСТАРІЛО: Синдром Міклесона | |
| zh | 弃用：Mickleson综合征 | |
| tr | Eski adı: Mickleson sendromu |
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.
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/2507
- This record as JSON: /data/d/2507.json