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MIM:607453 - DEAFNESS, AUTOSOMAL DOMINANT 44; DFNA44
Xenbase Genes: ccdc50
Human Disease Resource: MIM
MONDO:0011832 - autosomal dominant nonsyndromic hearing loss 44 |
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss |
DOID:0110569 - autosomal dominant nonsyndromic deafness 44 |