| C1863659 |
DEAFNESS, AUTOSOMAL DOMINANT 17 |
DO |
autosomal dominant nonsyndromic deafness 17
|
0110548 |
| C1863659 |
DEAFNESS, AUTOSOMAL DOMINANT 17 |
MONDO |
autosomal dominant nonsyndromic deafness 17
|
0011350 |
| C1863659 |
DEAFNESS, AUTOSOMAL DOMINANT 17 |
MSH |
MYH9-Related Disorders
|
C535507 |
| C1863659 |
DEAFNESS, AUTOSOMAL DOMINANT 17 |
MSH |
Sebastian syndrome
|
C535507 |
| C1863659 |
DEAFNESS, AUTOSOMAL DOMINANT 17 |
MSH |
Deafness, Autosomal Dominant 17
|
C535507 |
| C1863659 |
DEAFNESS, AUTOSOMAL DOMINANT 17 |
OMIM |
DEAFNESS, AUTOSOMAL DOMINANT 17
|
603622 |