autosomal recessive nonsyndromic deafness 99 (DOID:0111634)
Alliance: disease page
Synonyms: autosomal recessive deafness 99; DFNB99
Alt IDs: OMIM:618481
Definition: An autosomal recessive nonsyndromic deafness characterized by prelingual, severe to profound sensorineural hearing loss without vestibular dysfunction that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM132E gene on chromosome 17q12.