All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00886 - Chilblain lupus 610448 - - - TREX1 - -
00887 - Vasculopathy, retinal, with cerebral leukodystrophy 192315 - - - TREX1 - -
00885 AGS-1 Aicardi-Goutieres syndrome, type 1, dominant and recessive (AGS-1) 225750 - - - TREX1 - -
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 - -
01417 SLE lupus erythematosus, systemic, susceptibility to (SLE) 152700 - - - BANK1, C4A, CTLA4, DNASE1, FCGR2A, FCGR2B, PTPN22, TREX1 - -
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