Human genes for autosomal recessive nonsyndromic deafness 23
Autosomal recessive nonsyndromic deafness 23 [DOID:0110481]
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 PCDH15 gene on chromosome 10q21.
Synonyms: autosomal recessive nonsyndromic deafness 23, DOID:0110481, autosomal recessive deafness 23, DFNB23