All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02478 ADCADN ataxia, cerebellar, deafness, and narcolepsy, autosomal dominant 604121 AD 1 1 DNMT1 - -
03555 HSN1E neuropathy, sensory, hereditary, type IE (HSN-1E) 614116 AD - - DNMT1 - -
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