Human genes for autosomal recessive nonsyndromic deafness 79
Autosomal recessive nonsyndromic deafness 79 [DOID:0110526]
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 TPRN gene on chromosome 9q34.
Synonyms: autosomal recessive nonsyndromic deafness 79, DOID:0110526, autosomal recessive deafness 79, DFNB79