DISEASES

Disease-gene associations mined from literature

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,  DFNB28,  autosomal recessive deafness 28