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Summary Literature (0)
OMIM:603720 - DEAFNESS, AUTOSOMAL RECESSIVE 16; DFNB16

Xenbase Genes: strc

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011364 - autosomal recessive nonsyndromic hearing loss 16
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110471 - autosomal recessive nonsyndromic deafness 16