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
02297 - Helicobacter pylori infection, susceptibility to 600263 - - - IFNGR1, PTPRZ1 - -
02727 - Mycobacterium tuberculosis, susceptibility to 607948 - - - CCL2, CD209, CISH, IFNG, IFNGR1, IRGM, MC3R, SLC11A1, SP110, TIRAP, TLR2 - -
02823 anemia anemia, aplastic, incl. susceptibility to 609135 - 46 46 IFNG, NBN, PRF1, SBDS - -
02850 HIVS virus, human immunodeficiency, susceptibility to 609423 - 1 1 CCL11, CCL2, CCL3, CCL3L1, CD209, CX3CR1, CXCL12, CXCR1, HLA-C, IFNG, IL10, IL4R, KIR3DL1, TLR3 - -
01676 IMD27A immunodeficiency, type 27A, mycobacteriosis, AR (IMD-27A) 209950 AR 57 47 IFNGR1 - -
04508 IMD27B immunodeficiency, type 27B, mycobacteriosis, autosomal dominant (IMD-27B) 615978 AD 54 42 IFNGR1 - -
04509 IMD28 immunodeficiency, type 28, mycobacteriosis (IMD-28) 614889 AR 24 23 IFNGR2 - -
00189 TSC2 tuberous sclerosis, type 2 613254 AD 20 23 IFNG, TSC2 - -
02938 virus, Hepatitis B virus, Hepatitis B, susceptibility to 610424 - - - IFNAR2, IFNGR1 - -
02857 virus, Hepatitis C virus, Hepatitis C, susceptibility to 609532 - - - CCR5, IFNG, IFNL3 - -
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