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

Xenbase Genes: col11a2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011159 - primary subdivision of cranial skeletal system
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

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