Human genes for autosomal recessive nonsyndromic deafness 7
Autosomal recessive nonsyndromic deafness 7 [DOID:0110520]
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 TMC1 gene on chromosome 9q21.
Synonyms: autosomal recessive nonsyndromic deafness 7, DOID:0110520, autosomal recessive deafness 7, DFNB11, DFNB7