autosomal recessive nonsyndromic deafness 8 (DOID:0110527)
Alliance: disease page
Synonyms: autosomal recessive deafness 8; autosomal recessive deafness 10; childhood-onset neurosensory autosomal recessive deafness 8; DFNB8; DFNB10; neurosensory nonsyndromic recessive deafness 8; NRSD8
Alt IDs: OMIM:601072, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TMPRSS3 gene on chromosome 21q22.