Deafness, autosomal recessive nonsyndromic sensorineural 12 (medical condition)

Recessively inherited hearing loss that occurs without any other symptoms – i.e. is not associated with any other condition. Type 12 involves a defect of the cadherin-23 gene on chromosome 10q21-q22, 3p26-p25. See also Deafness, autosomal recessive 12