DISEASES

Disease-gene associations mined from literature

Human genes for autosomal recessive nonsyndromic deafness 68

Autosomal recessive nonsyndromic deafness 68 [DOID:0110519]

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the S1PR2 gene on chromosome 19p13.

Synonyms:  autosomal recessive nonsyndromic deafness 68,  DOID:0110519,  DFNB68,  autosomal recessive deafness 68