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, autosomal recessive deafness 68, DFNB68