Human genes for autosomal recessive nonsyndromic deafness 63
Autosomal recessive nonsyndromic deafness 63 [DOID:0110515]
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 LRTOMT gene on chromosome 11q13.
Synonyms: autosomal recessive nonsyndromic deafness 63, DOID:0110515, autosomal recessive deafness 63, DFNB63