autosomal dominant nonsyndromic deafness 41 (DOID:0110567)
Alliance: disease page
Synonyms: autosomal dominant deafness 41; DFNA41
Alt IDs: OMIM:608224, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the purinergic receptor P2X 2 gene (P2RX2) on chromosome 12q24.