autosomal recessive nonsyndromic deafness 9 (DOID:0110535)
Alliance: disease page
Synonyms: autosomal recessive deafness 9; DFNB9; neurosensory nonsyndromic recessive deafness 9; NRSD9
Alt IDs: OMIM:601071, ICD10CM:H90.3
Definition: 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.