Human genes for autosomal recessive nonsyndromic deafness 16
Autosomal recessive nonsyndromic deafness 16 [DOID:0110471]
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 STRC gene on chromosome 15q15.
Synonyms: autosomal recessive nonsyndromic deafness 16, DOID:0110471, autosomal recessive deafness 16, DFNB16