ORPHA:68361
Rare deafness
Synonyms: Rare hearing loss
- 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 deafness | Rare hearing loss |
| fr | Surdité rare | |
| de | Schwerhörigkeit, seltene | |
| es | Sordera rara | Hipoacusia rara |
| it | Sordità rara | |
| nl | Zeldzame doofheid | |
| pt | Surdez rara | Perda auditiva rara |
| pl | Rzadkie rodzaje głuchoty | = en |
| cs | Vzácné formy hluchoty | = en |
| uk | Рідкісна глухота | Рідкісна втрата слуху |
| zh | 罕见耳聋 | 罕见听力丧失 |
| tr | Nadir görülen sağırlık | Nadir işitme kaybı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19047 | E | validated | |
| UMLS | C5680167 | 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: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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/68361
- This record as JSON: /data/d/68361.json