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 )

Relationships
is a type of: autosomal dominant nonsyndromic deafness