Term Name:	autosomal dominant nonsyndromic deafness 41
Synonyms:	autosomal dominant deafness 41, DFNA41
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.
Ontology:	Human Disease [DOID:0110567]   ( DOID:0110567 )