All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06906 DEE encephalopathy, developmental and epileptic - - 272 274 ATP1A3, CELF2, DALRD3, DNM1, GAD1, GLUL, GNAO1, KCNA2, KCNH5, MDGA2, NEUROD2, NTRK2, TMEM63B - -
06818 DEE58 encephalopathy, developmental and epileptic, type 58 617830 AD 1 1 NTRK2 - -
03483 OBHD obesity, hyperphagia, developmental delay (OBHD) 613886 AD - - NTRK2 - -
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