ORPHA:93545
Renal or urinary tract malformation
Synonyms: CAKUT · Congenital anomalies of kidney and urinary tract
- 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 | Renal or urinary tract malformation | CAKUT · Congenital anomalies of kidney and urinary tract |
| fr | Malformation du rein et des voies urinaires | Anomalies congénitales du rein et des voies urinaires · CAKUT |
| de | Fehlbildung der Nieren oder Harnwege | CAKUT · Kongenitale Anomalien der Nieren und ableitenden Harnwege |
| es | Malformación del tracto urinario o renal | Anomalías congénitas del riñón y el tracto urinario · CAKUT |
| it | Malformazione del tratto urinario o renale | Anomalie congenite del rene e del tratto urinario · CAKUT |
| nl | Malformatie van nier of urinewegen | CAKUT · Congenitale anomalieën van nier en urinewegen |
| pt | Malformação renal ou do trato urinário | |
| pl | Malformacje nerek lub układu moczowego | CAKUT · Wrodzone wady nerek i układu moczowego |
| cs | Malformace ledvinného nebo močového traktu | CAKUT · Vrozené anomálie ledvinného a močového traktu |
| uk | Вади розвитку нирок або сечовивідних шляхів | CAKUT · Вроджені аномалії нирок та сечовивідних шляхів |
| zh | 肾或尿路畸形 | 肾和尿路先天性异常 |
| tr | Böbrek veya idrar yolu malformasyonu | CAKUT · Böbrek ve idrar yolunun doğumsal anomalileri |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019719 | E | validated | |
| MeSH | C566906 | E | validated | |
| UMLS | C1968949 | 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 (2):
- ORPHA:93890Rare developmental defect during embryogenesis
rare developmental anomalies during embryogenesis - ORPHA:93626Rare renal disease
rare renal 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/93545
- This record as JSON: /data/d/93545.json