autosomal recessive nonsyndromic deafness 31 (DOID:0110490)
Alliance: disease page
Synonyms: autosomal recessive deafness 31; DFNB31
Alt IDs: OMIM:607084, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the WHRN gene on chromosome 9q32.