ORPHA:156243
Pinnae and external auditory canal 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 | Pinnae and external auditory canal anomaly | |
| fr | Anomalie du pavillon de l'oreille et conduit auditif externe | |
| de | Ohrmuschel und äußerer Gehörgang, Anomalie | |
| es | Anomalía en el pabellón de la oreja y en el canal auditivo externo | |
| it | Anomalie del padiglione e condotto uditivo esterno | |
| nl | Oorschelp- en uitwendig gehoorkanaalanomalie | |
| pt | Anomalia auricular e do canal auditivo externo | |
| pl | Wada ślimaka i zewnętrznego przewodu słuchowego | |
| cs | Anomálie ušního boltce a zevního zvukovodu | |
| uk | Аномалія вушної раковини та зовнішнього слухового проходу | |
| zh | 耳廓及外耳道异常 | |
| tr | Pinnae ve eksternal işitsel kanal anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15502 | E | validated | |
| UMLS | C5680660 | 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:435603Genetic otorhinolaryngological malformation
rare genetic diseases - ORPHA:96333Rare otorhinolaryngological malformation
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases
Children (6):
- ORPHA:93976Anotia
- ORPHA:141074External auditory canal aplasia/hypoplasia
- ORPHA:3023External auditory canal atresia-vertical talus-hypertelorism syndrome
- ORPHA:83463Microtia
- ORPHA:397623Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome
- ORPHA:500188X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome
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/156243
- This record as JSON: /data/d/156243.json