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
03454 EPM epilepsy, myoclonic, progressive (EPM) - - 75 66 CSTB, GOSR2 - -
00009 EPM1A epilepsy, myoclonic, progressive, type 1A (EPM1A, Unverricht and Lundborg) 254800 AR 2 3 CSTB - -
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