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Deafness, autosomal recessive nonsyndromic sensorineural 37 (medical condition): Recessively inherited hearing loss that occurs without any other symptoms - i.e. is not associated with any other condition. Type 37 involves a defect of the myosin VI gene on chromosome 6q13.
See also:
Deafness, autosomal recessive 37:
»Introduction: Deafness, autosomal recessive 37
»Symptoms of Deafness, autosomal recessive 37
These medical condition or symptom topics may be relevant to medical information for Deafness, autosomal recessive nonsyndromic sensorineural 37:
Deafness, autosomal recessive nonsyndromic sensorineural 37: Another name for Deafness, autosomal recessive 37 (or close medical condition association).
»Introduction: Deafness, autosomal recessive 37
»Symptoms of Deafness, autosomal recessive 37
Some of the symptoms of Deafness, autosomal recessive nonsyndromic sensorineural 37 incude:
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