ORPHA:139015
OBSOLETE: Chondrodysplastic malformation syndrome
inactive · referred to ORPHA:139012Rare bone development disorder
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Rare bone development disorder
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Chondrodysplastic malformation syndrome | |
| fr | OBSOLETE : Syndrome malformatif chondrodysplasique | |
| de | OBSOLET: Chondrodysplasie-Syndrom | |
| es | OBSOLETO: Síndrome malformativo condrodisplásico | |
| it | OBSOLETO: Condrodisplasia | |
| nl | OBSOLEET: Chondrodysplastische malformatiesyndroom | |
| pt | OBSOLETO: Condrodisplasia | |
| pl | NIEAKTUALNE: Zespól malformacji chondrodysplastycznej | |
| cs | NEAKTUÁLNÍ: Syndrom chondrodysplastické malformace | |
| uk | ЗАСТАРІЛО: Синдром хондродиспластичної мальформації | |
| zh | 弃用：软骨发育不良型畸形综合征 | |
| tr | Eski adı: Kondrodisplastik malformasyon sendromu |
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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/139015
- This record as JSON: /data/d/139015.json