Human genes for autosomal recessive nonsyndromic deafness 28
Autosomal recessive nonsyndromic deafness 28 [DOID:0110486]
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 TRIOBP gene on chromosome 22q13.
Synonyms: autosomal recessive nonsyndromic deafness 28, DOID:0110486, autosomal recessive deafness 28, DFNB28