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
00841 EIEE encephalopathy, epileptic, early infantile (EIEE) - - 155 158 CELSR3, CPLX1, HNRNPU, ITPA, PHACTR1, RHOBTB2 - -
05591 EIEE64 encephalopathy, epileptic, early infantile, type 64 (EIEE-64) 618004 AD - - RHOBTB2 - autosomal dominant
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