Term Name:	autosomal recessive nonsyndromic deafness 111
Synonyms:	autosomal recessive deafness 111, DFNB111
Definition:	An autosomal recessive nonsyndromic deafness characterized by early-onset, moderate to severe sensorineural hearing loss with no vestibular involvement that has_material_basis_in homozygous or compound heterozygous mutation in the MPZL2 gene on chromosome 11q23.33.
Ontology:	Human Disease [DOID:0111640]   ( DOID:0111640 )