Term Name: autosomal dominant nonsyndromic deafness 22
Synonyms: autosomal dominant deafness 22, DFNA22
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 MYO6 gene on chromosome 6q14.
Ontology: Human Disease [DOID:0110552]   ( DOID:0110552 )

Relationships
is a type of: autosomal dominant nonsyndromic deafness