ORPHA:435365
Fetal lower urinary tract obstruction
Synonyms: LUTO
- Type
- Clinical group
- 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 | Fetal lower urinary tract obstruction | LUTO |
| fr | Obstruction du tractus urinaire inférieur | = en |
| de | Fetale Obstruktion der unteren Harnwege | = en |
| es | Obstrucción del tracto urinario inferior fetal | = en |
| it | Ostruzione fetale delle vie urinarie inferiori | = en |
| nl | Foetale obstructie van lagere urinewegen | = en |
| pt | Obstrução do trato urinário inferior fetal | |
| pl | Niedrożność dolnego odcinka dróg moczowych płodu | = en |
| cs | Fetální obstrukce dolního močového traktu | = en |
| uk | Обструкція нижніх сечових шляхів плода | = en |
| zh | 胎儿下尿路梗阻 | = en |
| tr | Fetal alt üriner sistem tıkanıklığı | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LB31.2 | E | specific | validated |
| MONDO | 0018559 | E | validated | |
| MONDO | 18559 | E | validated | |
| UMLS | C4305545 | 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 (3):
- ORPHA:357506Genetic non-syndromic renal or urinary tract malformation
rare genetic diseases - ORPHA:93546Non-syndromic renal or urinary tract malformation
rare developmental anomalies during embryogenesis; rare renal diseases; rare transplant-related disorders - ORPHA:182124Non-syndromic urogenital tract malformation of male and female
rare developmental anomalies during embryogenesis; rare urogenital diseases; rare transplant-related disorders
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/435365
- This record as JSON: /data/d/435365.json