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
05761 DEE54 encephalopathy, developmental and epileptic, type 54 617391 AD 1 1 HNRNPU - -
00841 EIEE encephalopathy, epileptic, early infantile (EIEE) - - 156 158 CELSR3, CPLX1, HNRNPU, ITPA, PHACTR1, RHOBTB2 - -
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