ORPHA:435609
Genetic larynx anomaly
- 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 | Genetic larynx anomaly | |
| fr | Anomalie du larynx d'origine génétique | |
| de | Larynx-Anomalie, genetisch bedingte | |
| es | Anomalía laríngea genética | |
| it | Anomalia genetica della laringe | |
| nl | Genetische anomalie van larynx | |
| pt | Anomalia da laringe genética | |
| pl | Genetyczna wada krtani | |
| cs | Geneticky podmíněná anomálie laryngu | |
| uk | Генетично обумовлена аномалія гортані | |
| zh | 遗传性喉异常 | |
| tr | Genetik gırtlak anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681173 | 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:435603Genetic otorhinolaryngological malformation
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/435609
- This record as JSON: /data/d/435609.json