ORPHA:357506
Genetic 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 | Genetic non-syndromic renal or urinary tract malformation | |
| fr | Anomalie génétique non syndromique du développement du rein et des voies urinaires | |
| de | Nieren/Harnwegsfehlbildung, nicht-syndromale, genetisch bedingte | |
| es | Malformación genética no sindrómica del tracto renal o urinario | |
| it | Malformazione genetica non sindromica del tratto urinario o renale | |
| nl | Genetische niet-syndromale nier- of urinewegmalformatie | |
| pt | Malformação genética renal ou urinária não sindromática | |
| pl | Genetyczne niesyndromiczne wady nerek lub układu moczowego | |
| cs | Dědičná nesyndromická malformace ledvinového nebo močového traktu | |
| uk | Генетично обумовлена несиндромальна вада розвитку нирок або сечовивідних шляхів | |
| zh | 遗传性非综合征性肾或尿路畸形 | |
| tr | Genetik, sendromik olmayan böbrek veya idrar yolu malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680986 | 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 (1):
- ORPHA:183539Genetic renal or urinary tract malformation
rare genetic diseases
Children (10):
- ORPHA:617Congenital primary megaureter
- ORPHA:237Duplication of urethra
- ORPHA:322Exstrophy-epispadias complex
- ORPHA:435365Fetal lower urinary tract obstruction
- ORPHA:1309Medullary sponge kidney
- ORPHA:1851Multicystic dysplastic kidney
- ORPHA:411709Renal agenesis
- ORPHA:93108Renal dysplasia
- ORPHA:93101Renal hypoplasia
- ORPHA:97369Renal tubular dysgenesis of genetic origin
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/357506
- This record as JSON: /data/d/357506.json