All diseases

11 entries on 1 page. Showing entries 1 - 11.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01861 CVID2 immunodeficiency, variable, common, type 2 (CVID-2) 240500 AD;AR - - CD19, CR2, ICOS, TNFRSF13B, TNFRSF13C - -
03349 CVID4 immunodeficiency, variable, common, type 4 (CVID-4) 613494 AR - - TNFRSF13C - -
01514 FEO osteolysis, familial expansile (FEO, McCabe disease) 174810 AD - - TNFRSF11A - -
01366 FPF fever, periodic, familial 142680 AD 1 1 TNFRSF1A - -
02107 HNSCC carcinoma, squamous cell, head and neck (HNSCC) 275355 AR 5 5 ING1, PTEN, TNFRSF10B - -
02856 IGAD2 immunoglobulin A deficiency, type 2 (IGAD-2) 609529 - - - TNFRSF13B - -
03731 MS5 multiple sclerosis susceptibility to, type 5 (MS-5) 614810 - - - TNFRSF1A - -
05611 NDD neurodevelopmental disorder (NDD) - - 3778 3593 ACBD6, ADARB1, AP1G1, ARFGEF1, ATP9A, CAMSAP1, CAPRIN1, CASP2, CHASERR, CPSF3L, DDB1, DENND5B, DHX30, DHX9, DOHH, DOT1L, EEFSEC, EIF2C1, EIF2C2, EIF4A2, 74 more - -
03117 OPTB7 osteopetrosis, autosomal recessive, type 7 (OPTB-7) 612301 AR 1 - TNFRSF11A - -
02411 PDB2 Paget disease of bone, type 2, early-onset (PDB-2) 602080 AD - - TNFRSF11A - -
01856 PDB5 Paget disease of bone, type 5, juvenile-onset (PDB-5, hyperphosphatasia) 239000 AR - - TNFRSF11B - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.