ORPHA:93216
OBSOLETE: Familial 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
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes | |
| fr | OBSOLETE : Syndrome néphrotique idiopathique familial corticorésistant à lésions glomérulaires minimes | OBSOLETE : Syndrome néphrotique idiopathique familial cortico-résistant à LGM · OBSOLETE : Syndrome néphrotique idiopathique familial corticorésistant à LGM |
| de | OBSOLET: Nephrotisches Syndrom, familiäres idiopathisches steroid-resistentes, mit Minimalläsionen | |
| es | OBSOLETO: Síndrome nefrótico familiar idiopático resistente a esteroides con cambios mínimos | |
| it | OBSOLETO: Sindrome nefrosica idiopatica steroido-resistente con alterazioni minime, forma familiare | |
| nl | OBSOLEET: Familiaal idiopathisch steroïderesistent nefrotisch syndroom met minimale verandering | |
| pt | OBSOLETO: Síndrome nefrótica corticorresistente idiopática familiar com alterações mínimas | |
| pl | NIEAKTUALNE: Rodzinny steroidooporny idiopatyczny zespól nerczycowy z minimalnymi zmianami | |
| cs | NEAKTUÁLNÍ: Familiární idiopatický nefrotický syndrom rezistentní na steroidy s minimálními změnami | |
| uk | ЗАСТАРІЛО: Сімейний ідіопатичний стероїдорезистентний нефротичний синдром з мінімальними змінами | |
| zh | 弃用：家族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 ailesel 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/93216
- This record as JSON: /data/d/93216.json