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Summary Literature (0)
MIM:607841 - DEAFNESS, AUTOSOMAL DOMINANT 48; DFNA48

Xenbase Genes: myo1a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011920 - autosomal dominant nonsyndromic hearing loss 48
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110571 - autosomal dominant nonsyndromic deafness 48