ORPHA:182124
Non-syndromic urogenital tract malformation of male and female
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-syndromic urogenital tract malformation of male and female | |
| fr | Malformation urogénitale non syndromique de l'homme et de la femme | |
| de | Urogenitale Fehlbildungen, weibliche und männliche, nichtsyndromale Formen | |
| es | Malformación no sindrómica del tracto urogenital masculino y femenino | |
| it | Malformazione non sindromica dell'apparato urogenitale maschile e femminile | |
| nl | Niet-syndromale malformatie van urogenitaal systeem van man en vrouw | |
| pt | Malformação do trato genito-urinário masculino e feminino não sindromática | |
| pl | Niesyndromiczna malformacja żeńskiego i męskiego układu moczowo-płciowego | |
| cs | Nesyndromické malformace urogenitálního traktu mužů a žen | |
| uk | Несиндромальна вада розвитку урогенітального тракту у чоловіків та жінок | |
| zh | 男性和女性非综合征性泌尿生殖道畸形 | |
| tr | Erkek ve dişinin non-endromik ürogenital sistem malformasyonu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15934 | E | validated | |
| UMLS | C5680594 | 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:165704Non-syndromic urogenital tract malformation
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare transplant-related disorders
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/182124
- This record as JSON: /data/d/182124.json