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Summary Literature (0)
OMIM:601868 - DEAFNESS, AUTOSOMAL DOMINANT 13; DFNA13


Xenbase Genes: col11a2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011159 - autosomal dominant nonsyndromic deafness 13

Disease Ontology (DO):
DOID:0110545 - autosomal dominant nonsyndromic deafness 13