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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)