Human genes for autosomal recessive nonsyndromic deafness 61
Autosomal recessive nonsyndromic deafness 61 [DOID:0110513]
An 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 SLC26A5 gene on chromosome 7q22.
Synonyms: autosomal recessive nonsyndromic deafness 61, DOID:0110513, autosomal recessive deafness 61, DFNB61