Term Name: autosomal dominant nonsyndromic deafness 3A
Synonyms: autosomal dominant deafness 3A, DFNA3A
Definition: An autosomal dominant nonsyndromic deafness that is characterized by prelingual, high frequency hearing loss and has_material_basis_in mutation in the GJB2 gene on chromosome 13q12.
Ontology: Human Disease [DOID:0110564]   ( DOID:0110564 )

Relationships
is a type of: autosomal dominant nonsyndromic deafness