Human genes for autosomal dominant nonsyndromic deafness 36
Autosomal dominant nonsyndromic deafness 36 [DOID:0110563]
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the TMC1 gene on chromosome 9q21.
Synonyms: autosomal dominant nonsyndromic deafness 36, DOID:0110563, autosomal dominant deafness 36, DFNA36