autosomal dominant nonsyndromic deafness 13 (DOID:0110545)
Alliance: disease page
Synonyms: autosomal dominant deafness 13; DFNA13
Alt IDs: OMIM:601868, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has_material_basis_in mutation in the COL11A2 gene on chromosome 6p21.