(Q28024616)
English
autosomal recessive nonsyndromic deafness 30
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutations in the MYO3A gene on chromosome 10p12.1.
- DFNB30
- autosomal recessive deafness 30
- DEAFNESS, AUTOSOMAL RECESSIVE 30
- DEAFNESS, AUTOSOMAL RECESSIVE 30; DFNB30
- Deafness, Autosomal Recessive type 30
- autosomal recessive nonsyndromic deafness type 30
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Identifiers
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