All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00841 EIEE encephalopathy, epileptic, early infantile (EIEE) - - 156 159 CELSR3, CPLX1, HNRNPU, ITPA, PHACTR1, RHOBTB2 - -
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