Term Name:	autosomal recessive nonsyndromic deafness 61
Synonyms:	autosomal recessive deafness 61, DFNB61
Definition:	An autosomal recessive nonsyndromic deafness that is characterized by early childhood-onset moderate to severe sensorineural hearing loss and has_material_basis_in mutation in the SLC26A5 gene on chromosome 7q22.
Ontology:	Human Disease [DOID:0110513]   ( DOID:0110513 )