Human genes for autosomal recessive nonsyndromic deafness 36
Autosomal recessive nonsyndromic deafness 36 [DOID:0110494]
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the ESPN gene on chromosome 1p36.
Synonyms: autosomal recessive nonsyndromic deafness 36, DOID:0110494, autosomal recessive deafness 36, DFNB36