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
03075 ECA6 epilepsy, childhood absence, type 6 (ECA-6) 611942 - 1 1 CACNA1H - -
05231 HALD4 hyperaldosteronism, familial, type IV (HALD41) 617027 AD - - CACNA1H - -
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