Human genes for autosomal recessive nonsyndromic deafness 31
Autosomal recessive nonsyndromic deafness 31 [DOID:0110490]
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the WHRN gene on chromosome 9q32.
Synonyms: autosomal recessive nonsyndromic deafness 31, DOID:0110490, autosomal recessive deafness 31