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
02682 EIG11;EJM8 epilepsy, idiopathic, generalized, susceptibility to, type 11 (EIG-11, epilepsy, myoclonic, juvenile, type 8(EJM-8)) 607628 AD - - CLCN2 - -
06552 HALD2 Hyperaldosteronism, familial, type II 605635 AD - - CLCN2 - -
04042 LKPAT leukoencephalopathy with ataxia 615651 AR - - CLCN2 - -
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