All diseases

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06906 DEE encephalopathy, developmental and epileptic - - 269 261 ATP1A3, CELF2, DALRD3, DNM1, GAD1, GLUL, GNAO1, KCNA2, KCNH5, NEUROD2, NTRK2, TMEM63B - -
03959 DEE17;EIEE17 developmental and epileptic encephalopathy, type 17 615473 AD 2 2 GNAO1 - -
06299 NEDIM Neurodevelopmental disorder with involuntary movements 617493 AD - - GNAO1 - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.