Term Name:	autosomal recessive nonsyndromic deafness 119
Synonyms:	DFNB119
Definition:	An autosomal recessive nonsyndromic deafness characterized by mild to profound sensorineural hearing loss that has_material_basis_in compound heterozygous mutation in the AFG2B gene on chromosome 15q21.
Ontology:	Human Disease [DOID:0070673]   ( DOID:0070673 )