(Q28024601)
English
autosomal recessive nonsyndromic deafness 1B
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has material basis in mutation in the GJB6 gene on chromosome 13q12
- DFNB1B
- autosomal recessive deafness 1B
- DEAFNESS, AUTOSOMAL RECESSIVE 1B
- autosomal recessive nonsyndromic deafness type 1B
- Deafness, Autosomal Recessive type 1B
- DEAFNESS, AUTOSOMAL RECESSIVE 1B; DFNB1B
Statements
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Identifiers
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