ORPHA:93220
OBSOLETE: Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
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
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis | |
| fr | OBSOLETE : Syndrome néphrotique idiopathique sporadique corticorésistant avec sclérose mésangiale diffuse | |
| de | OBSOLET: Nephrotisches Syndrom, idiopathisches steroid-resistentes, mit diffuser mesangialer Sklerose, sporadische Form | |
| es | OBSOLETO: Síndrome nefrótico esporádico idiopático resistente a esteroides con esclerosis mesangial difusa | |
| it | OBSOLETO: Sindrome nefrosica idiopatica steroido-resistente con sclerosi mesangiale diffusa, forma sporadica | |
| nl | OBSOLEET: Sporadisch idiopathisch steroïderesistent nefrotisch syndroom met diffuse mesangiale sclerose | |
| pt | OBSOLETO: Síndrome nefrótica corticorresistente idiopática esporádica com esclerose mesangial difusa | |
| pl | NIEAKTUALNE: Sporadyczny steroidooporny idiopatyczny zespól nerczycowy z rozlanym stwardnieniem mezangium | |
| cs | NEAKTUÁLNÍ: Sporadický idiopatický nefrotický syndrom rezistentní na steroidy s difuzní sklerózou mesangia | |
| uk | ЗАСТАРІЛО: Спорадичний ідіопатичний стероїдорезистентний нефротичний синдром з дифузним мезангіальним склерозом | |
| zh | 弃用：散发性激素敏感型原发性肾病综合征伴弥漫性系膜硬化 | |
| tr | Eski adı: Yaygın mezangial skleroz ile seyreden sporadik idiyopatik steroide dirençli nefrotik sendrom |
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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/93220
- This record as JSON: /data/d/93220.json