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
04070 EIEE19 encephalopathy, epileptic, early infantile, type 19 (EIEE-19) 615744 AD 12 11 GABRA1 - -
03012 EIG13;EJM5 epilepsy, idiopathic, generalized, susceptibility to, type 13 (EIG-13, epilepsy, myoclonic, juvenile, type 5 (EJM-5)) 611136 - - - GABRA1 - -
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