ORPHA:93546
Non-syndromic renal or urinary tract malformation
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-syndromic renal or urinary tract malformation | |
| fr | Anomalie non syndromique du développement du rein et des voies urinaires | |
| de | Nieren/Harnwegsfehlbildung, nicht-syndromale | |
| es | Malformación no sindrómica del tracto urinario o renal | |
| it | Malformazione non sindromica del tratto urinario o renale | |
| nl | Niet-syndromale malformatie van nier of urinewegen | |
| pt | Malformação renal ou do trato urinário não sindromática | |
| pl | Niesyndromiczne malformacje nerek lub układu moczowego | |
| cs | Nesyndromická malformace ledvinného nebo močového traktu | |
| uk | Несиндромальні вади розвитку нирок або сечовивідних шляхів | |
| zh | 非综合征型肾或尿路畸形 | |
| tr | Sendromik olmayan böbrek veya idrar yolu malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681585 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:506213Rare disorder potentially indicated for kidney transplant
rare transplant-related disorders - ORPHA:93545Renal or urinary tract malformation
rare developmental anomalies during embryogenesis; rare renal diseases
Children (16):
- ORPHA:93109Congenital megacalycosis
- ORPHA:617Congenital primary megaureter
- ORPHA:435743Congenital urachal anomaly
- ORPHA:237Duplication of urethra
- ORPHA:322Exstrophy-epispadias complex
- ORPHA:289365Familial vesicoureteral reflux
- ORPHA:435365Fetal lower urinary tract obstruction
- ORPHA:1309Medullary sponge kidney
- ORPHA:238637Megacystis-megaureter syndrome
- ORPHA:1851Multicystic dysplastic kidney
- ORPHA:2260Oligomeganephronia
- ORPHA:411709Renal agenesis
- ORPHA:93108Renal dysplasia
- ORPHA:93101Renal hypoplasia
- ORPHA:3033Renal tubular dysgenesis
- ORPHA:652528Supernumerary kidney
Codes that Orphanet moved or referred to this one:
- ORPHA:1849OBSOLETE: Infundibulopelvic stenosis-multicystic kidney syndrome referred to · inactive
- ORPHA:2190OBSOLETE: Congenital hydronephrosis referred to · inactive
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/93546
- This record as JSON: /data/d/93546.json