Disease #00040 (NSHL (non-syndromic hearing loss))
Official abbreviation |
NSHL |
Name |
non-syndromic hearing loss |
OMIM ID |
- |
Inheritance |
- |
Individuals reported having this disease |
8 |
Phenotype entries for this disease |
1 |
Associated with 2 genes |
GJB2, GJB6 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|