All diseases

6 entries on 1 page. Showing entries 1 - 6.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00885 AGS1 Aicardi-Goutieres syndrome, type 1, dominant and recessive (AGS1) 225750 AD;AR 42 42 TREX1 - -
05881 CHBL Chilblain lupus (CHBL) - - 0 0 SAMHD1, TREX1 - -
00886 CHBL1 Chilblain lupus, type 1 (CHBL1) 610448 AD 4 4 TREX1 - -
00139 ID intellectual disability (ID) - - 2195 1894 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 540 more - -
00887 RVCL vasculopathy, retinal, with cerebral leukodystrophy (RVCL) 192315 AD 7 7 TREX1 - -
01417 SLE lupus erythematosus, systemic, susceptibility to (SLE) 152700 AD 11 11 BANK1, C4A, CTLA4, DNASE1, FCGR2A, FCGR2B, PTPN22, TREX1 - -
Legend   How to query