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
05903 EPM11 epilepsy, progressive myoclonic, type 11 (EPM11) 608873 AD 1 1 SEMA6B - -
06450 EPM11 Epilepsy, progressive myoclonic, 11 618876 AD - - SEMA6B - -
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