Term Name: autosomal dominant nonsyndromic deafness 82
Synonyms: autosomal dominant deafness 82, DFNA82
Definition: An autosomal dominant nonsyndromic deafness characterized by onset of rapidly progressive bilateral sensorineural hearing loss usually early in the first decade that has_material_basis_in heterozygous mutation in the ATP2B2 gene on chromosome 3p25.1.
Ontology: Human Disease [DOID:0070603]   ( DOID:0070603 )

Relationships
is a type of: autosomal dominant nonsyndromic deafness