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

Xenbase Genes: strc

Human Disease Resource: MIM

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

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