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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 16-09-2013 |
Symbol | DFNB89 |
Location | 16q23.1 |
Name | nonsyndromic hearing impairment locus 89 |
Corresponding gene | KARS |
Other symbol(s) | ARNSHI |
Main clinical features | nonsyndromic hearing impairment in Pakistany consanguineous families PMID: 21181198 |
Genetic determination | autosomal recessive |
Function/system disorder | ear |
Type | disease |
Remark(s) |