Human genes for autosomal recessive nonsyndromic deafness 3
Autosomal recessive nonsyndromic deafness 3 [DOID:0110488]
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 MYO15A gene on chromosome 17p11.
Synonyms: autosomal recessive nonsyndromic deafness 3, DOID:0110488, autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3, DFNB3, NRSD3 ...