autosomal recessive nonsyndromic deafness 36 (DOID:0110494)
Alliance: disease page
Synonyms: autosomal recessive deafness 36; DFNB36
Alt IDs: OMIM:609006, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the ESPN gene on chromosome 1p36.