ORPHA:93221
OBSOLETE: Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes
inactive · referred to ORPHA:656Hereditary steroid-resistant nephrotic syndrome
- Type
- Histopathological subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Genetic steroid-resistant nephrotic syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes | |
| fr | OBSOLETE : Syndrome néphrotique idiopathique sporadique corticorésistant à lésions glomérulaires minimes | OBSOLETE : Syndrome néphrotique idiopathique sporadique cortico-résistant à LGM · OBSOLETE : Syndrome néphrotique idiopathique sporadique corticorésistant à LGM |
| de | OBSOLET: Nephrotisches Syndrom, idiopathisches steroid-resistentes, mit glomerulärer Minimalläsion, sporadische Form | |
| es | OBSOLETO: Síndrome nefrótico esporádico idiopático resistente a esteroides con cambios mínimos | |
| it | OBSOLETO: Sindrome nefrosica idiopatica steroido-resistente con alterazioni minime, forma sporadica | |
| nl | OBSOLEET: Sporadisch idiopathisch steroïderesistent nefrotisch syndroom met minimale verandering | |
| pt | OBSOLETO: Síndrome nefrótica corticorresistente idiopática esporádica com alterações mínimas | |
| pl | NIEAKTUALNE: Sporadyczny steroidooporny idiopatyczny zespól nerczycowy z minimalnymi zmianami | |
| cs | NEAKTUÁLNÍ: Sporadický idiopatický nefrotický syndrom rezistentní na steroidy s minimálními změnami | |
| uk | ЗАСТАРІЛО: Спорадичний ідіопатичний стероїдорезистентний нефротичний синдром з мінімальними змінами | |
| zh | 弃用：散发性激素敏感型原发性肾病综合征伴微小病变 | |
| tr | Eski adı: Minimal değişiklik ile seyreden sporadik idiyopatik steroide dirençli nefrotik sendrom |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/93221
- This record as JSON: /data/d/93221.json