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MIM:604121 - CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN
Xenbase Genes: dnmt1
Human Disease Resource: OMIM
MONDO:0011397 - autosomal dominant cerebellar ataxia, deafness and narcolepsy |
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MONDO:0011397 - autosomal dominant cerebellar ataxia, deafness and narcolepsy |