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Summary Literature (0)
MIM:609439 - DEAFNESS, AUTOSOMAL RECESSIVE 48; DFNB48

Xenbase Genes: cib2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012273 - periampullary region of duodenum
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110505 - autosomal recessive nonsyndromic deafness 48