Term Name: autosomal dominant nonsyndromic deafness 15
Synonyms: autosomal dominant deafness 15, autosomal dominant nonsyndromic deafness 52, DFNA15
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the POU4F3 gene on chromosome 5q32.
Ontology: Human Disease [DOID:0110546]   ( DOID:0110546 )

Relationships
is a type of: autosomal dominant nonsyndromic deafness