ORPHA:156619
Rare genetic urogenital disease
- 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 | Rare genetic urogenital disease | |
| fr | Maladie urogénitale génétique rare | |
| de | Urogenitale Anomalie, genetisch bedingte | |
| es | Anomalías urogenitales genéticas raras | |
| it | Anomalia urogenitale genetica | |
| nl | Zeldzame genetische urogenitale ziekte | |
| pt | Anomalia urogenital genética | |
| pl | Rzadka genetyczna choroba układu moczowo-płciowego | |
| cs | Vzácné geneticky podmíněné nemoci urogenitálního traktu | |
| uk | Рідкісне генетично обумовлене урогенітальне захворювання | |
| zh | 罕见的遗传性泌尿生殖疾病 | |
| tr | Nadir genetik ürogenital hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15511 | E | validated | |
| UMLS | C5680641 | 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 (1):
- ORPHA:98053Rare genetic 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/156619
- This record as JSON: /data/d/156619.json