ORPHA:1765
OBSOLETE: Dyschondrosteosis-nephritis syndrome
inactive · referred to ORPHA:93438Mesomelic and rhizo-mesomelic 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 Mesomelic and rhizo-mesomelic dysplasia
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Dyschondrosteosis-nephritis syndrome | |
| fr | OBSOLETE : Syndrome de dyschondrostéose-néphropathie | |
| de | OBSOLET: Dyschondrosteose-Nephritis-Syndrom | |
| es | OBSOLETO: Síndrome de discondrosteosis-nefropatía | |
| it | OBSOLETO: Discondrosteosi-nefrite | |
| nl | OBSOLEET: Dyschondrosteose - nefritis-syndroom | |
| pt | OBSOLETO: Síndrome de discondrosteose-nefrite | |
| pl | NIEAKTUALNE: Dyschondrosteoza - zespół nerczycowy | |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující dyschondrosteózu a nefritidu | |
| uk | ЗАСТАРІЛО: Синдром дихондростеозу-нефриту | |
| zh | 软骨生成障碍-肾炎综合征 | |
| tr | Diskondrosteoz-nefrit 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/1765
- This record as JSON: /data/d/1765.json