All diseases

4 entries on 1 page. Showing entries 1 - 4.
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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 - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
01004 SMS Smith-Magenis syndrome (SMS) 182290 - - - RAI1 - -
04119 TAM-2 myopathy, tubular aggregates, type 2 (TAM-2) 615883 - - - ORAI1 - -
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