Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GRXCR2 gene.
Comprehensive, easy-to-understand information about this condition
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autosomal recessive nonsyndromic hearing loss 5
MONDO:0000912
autosomal recessive nonsyndromic hearing loss 1A
MONDO:0009076
autosomal recessive nonsyndromic hearing loss 2
MONDO:0010807
autosomal recessive nonsyndromic hearing loss 3
MONDO:0010860
autosomal recessive nonsyndromic hearing loss 4
MONDO:0010933
autosomal recessive nonsyndromic hearing loss 6
MONDO:0010965