Human genes for autosomal recessive nonsyndromic deafness 25
Autosomal recessive nonsyndromic deafness 25 [DOID:0110483]
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the GRXCR1 gene on chromosome 4p13.
Synonyms: autosomal recessive nonsyndromic deafness 25, DOID:0110483, autosomal recessive deafness 25, DFNB25