Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the P2RX2 gene.
Comprehensive, easy-to-understand information about this condition
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autosomal dominant nonsyndromic hearing loss 1
MONDO:0007424
autosomal dominant nonsyndromic hearing loss 2A
MONDO:0010817
autosomal dominant nonsyndromic hearing loss 4A
MONDO:0010915
autosomal dominant nonsyndromic hearing loss 6
MONDO:0010963
autosomal dominant nonsyndromic hearing loss 5
MONDO:0010973
autosomal dominant nonsyndromic hearing loss 10
MONDO:0011031