autosomal recessive nonsyndromic deafness 115 (DOID:0111643)
Alliance: disease page
Synonyms: autosomal recessive deafness 115; DFNB115
Alt IDs: OMIM:618457
Definition: An autosomal recessive nonsyndromic deafness characterized by onset in early childhood of severe sensorineural hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in the SPNS2 gene on chromosome 17p13.2.