ORPHA:665
Albright hereditary osteodystrophy
inactive · moved to ORPHA:97593Pseudohypoparathyroidism
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Pseudohypoparathyroidism
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Albright hereditary osteodystrophy | |
| fr | Ostéodystrophie héréditaire d'Albright | |
| de | Albright-Osteodystrophie, hereditäre | Osteodystrophie, hereditäre Albright'sche |
| es | Osteodistrofia hereditaria de Albright | |
| it | Osteodistrofia ereditaria di Albright | |
| nl | Albright erfelijke osteodystrofie | |
| pt | Osteodistrofia hereditária de Albright | |
| pl | Dziedziczna osteodystrofia Albrighta | |
| cs | Albrightova hereditární osteodystrofie | |
| uk | Спадкова остеодистрофія Олбрайта | |
| zh | Albright遗传性骨营养不良症 | |
| tr | Albright kalıtsal osteodistrofisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C2931404 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
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/665
- This record as JSON: /data/d/665.json