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
03189 - Immune dysfunction with T-cell inactivation due to calcium entry defect 1 612782 - - - ORAI1 - -
04119 TAM-2 myopathy, tubular aggregates, type 2 (TAM-2) 615883 - - - ORAI1 - -
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