ORPHA:96210
Rare genetic deafness
Synonyms: Rare genetic 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 genetic deafness | Rare genetic hearing loss |
| fr | Surdité génétique rare | |
| de | Schwerhörigkeit, genetisch bedingte | |
| es | Sordera rara genética | Hipoacusia rara genética |
| it | Sordità genetica | |
| nl | Zeldzame genetische doofheid | |
| pt | Surdez genética | |
| pl | Rzadka głuchota genetyczna | = en |
| cs | Vzácná genetická ztráta sluchu | = en |
| uk | Рідкісна генетично обумовлена глухота | Рідкісна генетична втрата слуху |
| zh | 罕见遗传性耳聋 | 罕见遗传性听力丧失 |
| tr | Nadir görülen genetik sağırlık | Nadir genetik işitme kaybı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680250 | 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:466084Genetic otorhinolaryngologic disease
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/96210
- This record as JSON: /data/d/96210.json