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Summary Literature (0)
MIM:604121 - CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN


Xenbase Genes: dnmt1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011397 - autosomal dominant cerebellar ataxia, deafness and narcolepsy