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
01861 CVID-2 immunodeficiency, variable, common, type 2 (CVID-2) 240500 - - - CD19, CR2, ICOS, TNFRSF13B, TNFRSF13C - -
03349 CVID-4 immunodeficiency, variable, common, type 4 (CVID-4) 613494 - - - TNFRSF13C - -
02107 HNSCC carcinoma, squamous cell, head and neck (HNSCC) 275355 - - - ING1, PTEN, TNFRSF10B - -
02856 IGAD-2 immunoglobulin A deficiency, type 2 (IGAD-2) 609529 - - - TNFRSF13B - -
03731 MS-5 multiple sclerosis susceptibility to, type 5 (MS-5) 614810 - - - TNFRSF1A - -
03117 OPTB-7 osteopetrosis, autosomal recessive, type 7 (OPTB-7) 612301 - - - TNFRSF11A - -
01514 PDB-2 Paget disease of bone, type 2, early-onset (PDB-2, expansile osteolysis) 174810 - - - TNFRSF11A - -
02411 PDB-2 Paget disease of bone, type 2, early-onset (PDB-2) 602080 - - - SQSTM1, TNFRSF11A - -
01856 PDB-5 Paget disease of bone, type 5, juvenile-onset (PDB-5, hyperphosphatasia) 239000 - - - TNFRSF11B - -
01366 TRAPS TNF receptor-associated periodic fever syndrome (TRAPS) 142680 - - - TNFRSF1A - -
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