autosomal recessive nonsyndromic deafness 59 (DOID:0110511)
Alliance: disease page
Synonyms: autosomal recessive deafness 59; DFNB59
Alt IDs: OMIM:610220, ICD10CM:H90.3
Definition: 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 DFNB59 gene on chromosome 2q31.