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
06200 CHEDDA Congenital hypotonia, epilepsy, developmental delay, and digital anomalies 618494 AD - - ATN1 - -
01280 DRPLA atrophy, pallidoluysian, dentatorubral (DRPLA) 125370 AD 57 57 ATN1 - -
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