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
05435 DEE92;IECEE2 encephalopathy, developmental and epileptic, type92 (IECEE2) 617829 AD 1 1 GABRB2 - autosomal dominant
05436 IECEE encephalopathy, epileptic, infantile or early childhood (IECEE) - - 1 1 GABRB2 - -
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