ORPHA:96333
Rare otorhinolaryngological malformation
- 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 otorhinolaryngological malformation | |
| fr | Malformation otorhinolaryngologique rare | |
| de | Otorhinolaryngologische Fehlbildung, seltene | |
| es | Malformación otorrinolaringológica rara | |
| it | Malformazione rara d'interesse otorinolaringoiatrico | |
| nl | Zeldzame otorinolaryngologische malformatie | |
| pt | Malformação otorrinolaringológica, rara | |
| pl | Rzadka malformacja uszno-nosowo-krtaniowa | |
| cs | Vzácné otorinolaryngologické malformace | Vzácné ORL malformace |
| uk | Рідкісна оториноларингологічна вада розвитку | |
| zh | 罕见耳鼻喉畸形 | |
| tr | Nadir kulak burun boğaz malformasyonu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681539 | 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 (2):
- ORPHA:155832Rare head and neck malformation
rare developmental anomalies during embryogenesis - ORPHA:98036Rare otorhinolaryngologic disease
rare otorhinolaryngological 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/96333
- This record as JSON: /data/d/96333.json