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Summary Literature (0)
MIM:616357 - DEAFNESS, AUTOSOMAL DOMINANT 40; DFNA40

Xenbase Genes: crym

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014603 - autosomal dominant nonsyndromic hearing loss 40
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss