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Summary Literature (0)
MIM:607821 - DEAFNESS, AUTOSOMAL RECESSIVE 37; DFNB37

Xenbase Genes: myo6

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011912 - autosomal recessive nonsyndromic hearing loss 37
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110495 - autosomal recessive nonsyndromic deafness 37