All diseases

13 entries on 1 page. Showing entries 1 - 13.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02727 - Mycobacterium tuberculosis, susceptibility to 607948 - - - CCL2, CD209, CISH, IFNG, IFNGR1, IRGM, MC3R, SLC11A1, SP110, TIRAP, TLR2 - -
03324 - Birbeck granule deficiency 613393 - - - CD207 - -
01782 FANCD2 Fanconi anemia, complementation group D2 (FANCD-2) 227646 AR 41 41 FANCD2 - -
02710 FSGS3 glomerulosclerosis, segmental, focal, type 3, susceptibility to (FSGS-3) 607832 - - - CD2AP - -
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 - -
00139 ID intellectual disability (ID) - - 2752 2434 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 555 more - -
02910 IMD25 Immunodeficiency, type 25 610163 AR - - CD247 - -
03836 LPFS2 Lymphoproliferative syndrome 2 615122 AR 1 1 CD27 - -
01546 RA arthritis, rheumatoid (RA) 180300 - - - CD244, CIITA, HLA-DRB1, IL10, NFKBIL1, PADI4, PTPN22, SLC22A4 - -
06340 SGD2 Specific granule deficiency 2 617475 AR - - SMARCD2 - -
03888 SMALED2A atrophy, muscular, spinal, lower extremity predominant, type 2A 615290 AD 2 2 BICD2 - autosomal dominant inheritance
06825 SMALED2B spinal muscular atrophy, lower extremity-predominant, type 2B 618291 AD - - BICD2 - -
03615 virus, Dengue virus, Dengue, susceptibility to 614371 - - - CD209 - -
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