All diseases

10 entries on 1 page. Showing entries 1 - 10.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01676 - Disseminated atypical mycobacterial infection 209950 - - - IFNGR1, IFNGR2, IL12RB1, STAT1 - -
02297 - Helicobacter pylori infection, susceptibility to 600263 - - - IFNGR1, PTPRZ1 - -
02727 - Mycobacterium tuberculosis, susceptibility to 607948 - - - CD209, CISH, IFNG, IFNGR1, IRGM, MC3R, SLC11A1, SP110, TIRAP, TLR2 - -
02823 - Aplastic anemia 609135 - - - IFNG, NBN, PRF1, SBDS - -
02850 - virus, human immunodeficiency, susceptibility to 609423 - - - CCL11, CCL3, CD209, CX3CR1, CXCL12, CXCR1, HLA-C, IFNG, IL10, IL4R, KIR3DL1, TLR3 - -
02857 - Hepatitis c virus, susceptibility to 609532 - - - CCR5, IFNG, PTPRC - -
02938 - Hepatitis b virus, susceptibility to 610424 - - - IFNAR2, IFNGR1 - -
04508 IMD-27B immunodeficiency, type 27B, mycobacteriosis, autosomal dominant (IMD-27B) 615978 - - - IFNGR1 - -
04509 IMD-28 immunodeficiency, type 28, mycobacteriosis (IMD-28) 614889 - - - IFNGR2 - -
00189 TSC-2 tuberous sclerosis, type 2 (TSC-2) 613254 - - - IFNG, TSC2 - -
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