Human genes for autosomal recessive nonsyndromic deafness 9
Autosomal recessive nonsyndromic deafness 9 [DOID:0110535]
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOF gene on chromosome 2p23.
Synonyms: autosomal recessive nonsyndromic deafness 9, DOID:0110535, autosomal recessive deafness 9, DFNB9, neurosensory nonsyndromic recessive deafness 9 ...