Term Name:	autosomal dominant nonsyndromic deafness 69
Synonyms:	autosomal dominant deafness 69, DCUA, DFNA69, unilateral or asymmetric congenital deafness
Definition:	An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21.
Ontology:	Human Disease [DOID:0110590]   ( DOID:0110590 )