autosomal recessive nonsyndromic deafness 16 (DOID:0110471)
Alliance: disease page
Synonyms: autosomal recessive deafness 16; DFNB16
Alt IDs: OMIM:603720, 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 STRC gene on chromosome 15q15.