Home Page |
References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 25-02-2016 |
Symbol | DFNB68 |
Location | 19p13.2 |
Name | neurosensory deafness 68 |
Corresponding gene | S1PR2 |
Main clinical features |
|
Genetic determination | autosomal recessive |
Function/system disorder | ear |
Type | disease |
Remark(s) |