ORPHA:567550
Idiopathic multidrug-resistant nephrotic syndrome
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Idiopathic multidrug-resistant nephrotic syndrome | |
| fr | Syndrome néphrotique idiopathique avec résistance multiple aux médicaments | |
| de | Idiopathisches MDR-resistentes nephrotisches Syndrom | |
| es | Síndrome nefrótico idiopático resistente a múltiples fármacos | |
| it | Sindrome nefrosica idiopatica multifarmaco-resistente | |
| nl | Idiopathisch multidrugresistent nefrotisch syndroom | |
| pt | Síndrome nefrótico multiresistente a fármacos idiopático | |
| pl | Idiopatyczny zespół nerczycowy oporny na leki | |
| cs | Idiopatický multirezistentní nefrotický syndrom | |
| uk | Ідіопатичний мультирезистентний нефротичний синдром | |
| zh | 特发性耐多药肾病综合征 | |
| tr | İdiyopatik çoklu ilaca dirençli nefrotik sendrom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | N04.8 | NTBT | attributed | validated |
| MONDO | 0035459 | E | validated | |
| UMLS | C5681293 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:567548Idiopathic steroid-resistant nephrotic syndrome
rare renal diseases; rare transplant-related disorders
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
6
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/567550
- This record as JSON: /data/d/567550.json