Human genes for autosomal recessive nonsyndromic deafness 76
Autosomal recessive nonsyndromic deafness 76 [DOID:0110524]
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with high frequency, progressive hearing loss and has_material_basis_in mutation in the SYNE4 gene on chromosome 19q13.
Synonyms: autosomal recessive nonsyndromic deafness 76, DOID:0110524, autosomal recessive deafness 76, DFNB76