DISEASES

Disease-gene associations mined from literature

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,  DFNB3,  NRSD3,  autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3 ...