Human genes for autosomal recessive nonsyndromic deafness 77
Autosomal recessive nonsyndromic deafness 77 [DOID:0110525]
An autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the LOXHD1 gene on chromosome 18q21.
Synonyms: autosomal recessive nonsyndromic deafness 77, DOID:0110525, autosomal recessive deafness 77, DFNB77