autosomal recessive nonsyndromic deafness 67 (DOID:0110518)
Alliance: disease page
Synonyms: autosomal recessive deafness 67; DFNB67
Alt IDs: OMIM:610265, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the LHFPL5 gene on chromosome 6p21.