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Summary Literature (0)
MIM:614035 - DEAFNESS, AUTOSOMAL RECESSIVE 29; DFNB29

Xenbase Genes: cldn14

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013537 - autosomal recessive nonsyndromic hearing loss 29
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110487 - autosomal recessive nonsyndromic deafness 29