Term Name: autosomal dominant nonsyndromic deafness 88
Synonyms: autosomal dominant deafness 88, DFNA88
Definition: An autosomal dominant nonsyndromic deafness characterized by postlingual progressive severe sensorineural hearing loss with tinnitus that has_material_basis_in heterozygous mutation in the EPHA10 gene on chromosome 1p34.
Ontology: Human Disease [DOID:0070611]   ( DOID:0070611 )

Relationships
is a type of: autosomal dominant nonsyndromic deafness