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
03111 ECA5 epilepsy, childhood absence, type 5 (ECA-5) 612269 - - - GABRB3 - -
06264 EIEE43 Epileptic encephalopathy, early infantile, 43 617113 AD - - GABRB3 - -
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