All diseases

16 entries on 1 page. Showing entries 1 - 16.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00511 - asthma, susceptibility to 600807 - 1 1 ADRB2, ALOX5, CCL11, HLA-G, HNMT, IL13, MUC7, PHF11, PLA2G7, SCGB3A2, TNF - -
01861 CVID-2 immunodeficiency, variable, common, type 2 (CVID-2) 240500 - 0 0 CD19, CR2, ICOS, TNFRSF13B, TNFRSF13C - -
03349 CVID-4 immunodeficiency, variable, common, type 4 (CVID-4) 613494 - 0 0 TNFRSF13C - -
01514 FEO osteolysis, familial expansile (FEO, McCabe disease) 174810 - 0 0 TNFRSF11A - -
02107 HNSCC carcinoma, squamous cell, head and neck (HNSCC) 275355 - 4 4 ING1, PTEN, TNFRSF10B - -
02856 IGAD-2 immunoglobulin A deficiency, type 2 (IGAD-2) 609529 - 0 0 TNFRSF13B - -
04020 IMD-16 immunodeficiency, type 16 (IMD-16) 615593 - 0 0 TNFRSF4 - -
02559 LORD retinal degeneration, late-onset (LORD) 605670 AD 0 0 C1QTNF5 - -
02760 MCI-1 myocardial infarction, susceptibility to, type 1 (MCI-1) 608446 - 41 2 ESR1, F13A1, F7, GCLC, GCLM, ITGB3, LGALS2, LTA, MIAT, OLR1, PSMA6, TNFSF4 - -
00309 MLRS malaria, susceptibility to, resistance (MLRS) 611162 - 0 0 CD36, CISH, CR1, DARC, FCGR2A, FCGR2B, G6PD, GYPA, GYPB, GYPC, HBB, ICAM1, NOS2, SLC4A1, TIRAP, TNF - -
03731 MS-5 multiple sclerosis susceptibility to, type 5 (MS-5) 614810 - 0 0 TNFRSF1A - -
01992 OPTB-2 osteopetrosis, autosomal recessive, type 2 (OPTB-2) 259710 - 0 0 TNFSF11 - -
03117 OPTB-7 osteopetrosis, autosomal recessive, type 7 (OPTB-7) 612301 - 0 0 TNFRSF11A - -
02411 PDB-2 Paget disease of bone, type 2, early-onset (PDB-2) 602080 - 0 0 TNFRSF11A - -
01856 PDB-5 Paget disease of bone, type 5, juvenile-onset (PDB-5, hyperphosphatasia) 239000 - 0 0 TNFRSF11B - -
01366 TRAPS TNF receptor-associated periodic fever syndrome (TRAPS) 142680 - 0 0 TNFRSF1A - -
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