Deafness, Autosomal Recessive 3 (MYO15A)

Deafness autosomal recessive 3 is a disorder caused by pathogenic variants in the gene MYO15A. Symptoms are present from birth with profound, nonsyndromic sensorineural hearing loss. Life expectancy is normal. This disorder has a higher incidence in an Indonesian village called Bengkala. No clear genotype-phenotype correlation has been established.

For information about carrier frequency and residual risk, please see the residual risk table.

This gene is included on the following panel(s):