Term Name: autosomal dominant nonsyndromic deafness 6
Synonyms: autosomal dominant deafness 14, autosomal dominant deafness 38, autosomal dominant deafness 6, DFNA14, DFNA38, DFNA6, DFNA6/14/38
Definition: An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has_material_basis_in mutation in the WFS1 gene on chromosome 4p16.
Ontology: Human Disease [DOID:0110584]   ( DOID:0110584 )

Relationships
is a type of: autosomal dominant nonsyndromic deafness