DISEASES

Disease-gene associations mined from literature

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