ORPHA:183539
Genetic 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 renal or urinary tract malformation | |
| fr | Malformation rénale ou des voies urinaires de cause génétique | |
| de | Nieren/Harnwegsfehlbildung, genetisch bedingte | |
| es | Malformación renal o de las vías urinarias de origen genético | |
| it | Malformazione genetica renale e dell'apparato urinario | |
| nl | Genetische renale of urinewegmalformatie | |
| pt | Malformação genética renal ou do trato urinário | |
| pl | Wada nerek lub układu moczowego uwarunkowana genetycznie | |
| cs | Geneticky podmíněné malformace ledvin nebo močových cest | |
| uk | Генетично обумовлена вада нирок або сечовивідних шляхів | |
| zh | 遗传性肾脏/输尿管多发畸形 | |
| tr | Genetik böbrek veya idrar yolu malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680556 | 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:183530Rare genetic developmental defect during embryogenesis
rare genetic diseases - ORPHA:98056Rare genetic renal disease
rare genetic diseases
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/183539
- This record as JSON: /data/d/183539.json