DISEASES

Disease-gene associations mined from literature

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