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) - - 76 67 CSTB, GOSR2 - -
03514 EPM6 epilepsy, myoclonic, progressive, type 6 (EPM-6) 614018 AR 13 13 GOSR2 - autosomal recessive
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