DISEASES

Disease-gene associations mined from literature

Human genes for autosomal recessive nonsyndromic deafness 61

Autosomal recessive nonsyndromic deafness 61 [DOID:0110513]

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 SLC26A5 gene on chromosome 7q22.

Synonyms:  autosomal recessive nonsyndromic deafness 61,  DOID:0110513,  DFNB61,  autosomal recessive deafness 61