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
00139 ID intellectual disability (ID) - - 2694 2376 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
03189 IMD9 Immunodeficiency, type 9 612782 AR - - ORAI1 - -
01004 SMS Smith-Magenis syndrome (SMS) 182290 AD;IC 6 6 RAI1 - -
04119 TAM2 myopathy, tubular aggregates, type 2 615883 AD 9 9 ORAI1 - -
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