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Summary Literature (0)
OMIM:500008 - DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL


Xenbase Genes: mt-co1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010779 - mitochondrial non-syndromic sensorineural hearing loss

Disease Ontology (DO):
DOID:0111751 - mitochondrial nonsyndromic sensorineural deafness