(Q28024645)
English
autosomal recessive nonsyndromic deafness 67
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the LHFPL5 gene on chromosome 6p21
- DFNB67
- autosomal recessive deafness 67
- Deafness, Autosomal Recessive type 67
- DEAFNESS, AUTOSOMAL RECESSIVE 67
- DEAFNESS, AUTOSOMAL RECESSIVE 67; DFNB67
- autosomal recessive nonsyndromic deafness type 67
Statements
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Identifiers
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