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MIM:600101 - DEAFNESS, AUTOSOMAL DOMINANT 2A; DFNA2A
Xenbase Genes: gjb3, kcnq4
Human Disease Resource: OMIM
MONDO:0010817 - autosomal dominant nonsyndromic hearing loss 2A |
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss |
DOID:0110558 - autosomal dominant nonsyndromic deafness 2A |