ORPHA:83001
Urogenital 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 | Urogenital tract malformation | |
| fr | Malformation urogénitale | |
| de | Urogenitale Fehlbildungen | |
| es | Malformación del tracto urogenital | |
| it | Malformazione del tratto urogenitale | |
| nl | Urogenitaal kanaalmalformatie | |
| pt | Malformação do trato urogenital | |
| pl | Malformacje układu moczowo-płciowego | |
| cs | Malformace urogenitálního traktu | |
| uk | Вади розвитку сечостатевих шляхів | |
| zh | 泌尿生殖道畸形 | |
| tr | Ürogenital sistem malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019356 | E | validated | |
| MONDO | 19356 | E | validated | |
| UMLS | C0042063 | E | validated | |
| MedDRA | 10062334 | 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:93890Rare developmental defect during embryogenesis
rare developmental anomalies during embryogenesis - ORPHA:101433Rare urogenital disease
rare urogenital 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/83001
- This record as JSON: /data/d/83001.json