Human genes for autosomal dominant nonsyndromic deafness 41
Autosomal dominant nonsyndromic deafness 41 [DOID:0110567]
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.
Synonyms: autosomal dominant nonsyndromic deafness 41, DOID:0110567, autosomal dominant deafness 41, DFNA41