nonsyndromic genetic hearing loss
MONDO:0019497Also known as: nonsyndromic deafness, nonsyndromic hearing loss, nonsyndromic genetic hearing loss, familial deafness, isolated genetic deafness
- MONDO:
- MONDO:0019497
- Orphanet:
- 87884 ↗
Rare disease72 associated genes
Description
A disease characterized by hearing loss that is not part of a larger syndrome.
Associated genes
+62 more genes — install the extension to see the full list inline on any page.