autosomal recessive nonsyndromic deafness 30 (DOID:0110489)
Alliance: disease page
Synonyms: autosomal recessive deafness 30; DFNB30
Alt IDs: OMIM:607101, ICD10CM:H90.3, ORDO:90636
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutations in the MYO3A gene on chromosome 10p12.1.