ORPHA:164004
Middle and/or inner ear 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Middle and/or inner ear anomaly | |
| fr | Anomalie de l'oreille moyenne et/ou interne | |
| de | Anomalie des Mittel- und/oder Innenohrs | |
| es | Anomalía del oído medio y/o interno | |
| it | Anomalia dellorecchio medio e/o interno | |
| nl | Anomalie van midden- en/of binnenoor | |
| pt | Anomalia do ouvido médio e/ou interno | |
| pl | Anomalia ucha środkowego | Anomalia ucha środkowego i/lub wewnętrznego |
| cs | Anomálie středního ucha | |
| uk | Аномалія середнього та/або внутрішнього вуха | |
| zh | 中耳畸形 | |
| tr | Orta kulak anomalisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15604 | E | validated | |
| UMLS | C5816681 | E | validated | |
| MedDRA | 10060957 | 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 (1):
- ORPHA:96333Rare otorhinolaryngological malformation
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/164004
- This record as JSON: /data/d/164004.json