acute retinal necrosis syndrome | | ISO | RGD:1352836 | 7365119 | DNA:polymorphisms:cds:HLA-Bw62 human | RGD | |
alopecia | | ISO | RGD:1352836 | 7387278 | human gene in rat model, DNA:polymorphisms:cds:HLA-B*2705 human | RGD | |
ankylosing spondylitis | susceptibility | ISO | RGD:1352836 | 7364914 | DNA:polymorphisms:cds:HLA-B27 more ... | RGD | |
anterior uveitis | | ISO | RGD:1352836 | 7364913 | DNA:polymorphisms:cds:HLA-B27 human, Thai | RGD | |
arthritis | | ISO | RGD:1352836 | 7364930 | associated with Inflammatory Bowel Diseases more ... | RGD | |
Behcet's disease | disease_progression | ISO | RGD:1352836 | 7364918 | DNA:polymorphisms:cds:HLA-B*15 human | RGD | |
Behcet's disease | | ISO | RGD:1352836 | 7364873 | DNA:polymorphisms:cds:HLA-B*51 human | RGD | |
Behcet's disease | no_association | ISO | RGD:1352836 | 7364939 | severe disease more ... | RGD | |
birdshot chorioretinopathy | | ISO | RGD:1352836 | 7365121 | DNA:polymorphisms:cds:HLA-B12 human | RGD | |
Choroidal Neovascularization | susceptibility | ISO | RGD:1352836 | 7365097 | associated with Macular Degeneration, DNA:polymorphisms:cds:HLA-B27 human | RGD | |
colitis | | ISO | RGD:1352836 | 7387221 | human gene in rat model, DNA:polymorphisms:cds:HLA-B27 human | RGD | |
cytomegalovirus retinitis | | ISO | RGD:1352836 | 7365106 | associated with HIV Infections more ... | RGD | |
dermatitis | | ISO | RGD:1352836 | 7387278 | human gene in rat model, DNA:polymorphisms:cds:HLA-B*2705 human | RGD | |
diabetic retinopathy | susceptibility | ISO | RGD:1352836 | 7365095 | associated with Diabetes Mellitus more ... | RGD | |
Eales Disease | | ISO | RGD:1352836 | 7365108 | DNA:polymorphisms more ... | RGD | |
erythema nodosum | | ISO | RGD:1352836 | 7364926 | associated with Inflammatory Bowel Diseases, DNA:polymorphisms:cds:multiple human | RGD | |
Experimental Autoimmune Uveitis | treatment | ISO | RGD:1352836 | 7364916 | human HLA-B27 peptide in rat model | RGD | |
Experimental Autoimmune Uveitis | treatment | ISO | RGD:1352836 | 7364942 | human peptide in rat model, HLA-B27 | RGD | |
Graves' disease | susceptibility | ISO | RGD:1352836 | 7365112 | DNA:polymorphisms, haplotype:cds:HLA-B8 human | RGD | |
Graves' disease | | ISO | RGD:1352836 | 7365110 | DNA:polymorphisms:cds:HLA-B39 human | RGD | |
Graves' disease | onset | ISO | RGD:1352836 | 7365118 | DNA:polymorphisms:cds:HLA-B8 human | RGD | |
Graves' disease | susceptibility | ISO | RGD:1352836 | 7365094 | DNA:polymorphisms:cds:HLA-B*46 human | RGD | |
Graves' disease | susceptibility | ISO | RGD:1352836 | 7365098 | DNA:polymorphisms, haplotype:cds:HLA-B*5801 human | RGD | |
Hearing Loss | | ISO | RGD:1352836 | 7364915 | associated with Behcet Syndrome, DNA:polymorphisms:cds:HLA-B51 human | RGD | |
histoplasmosis | | ISO | RGD:1352836 | 7364917 | Presumed Ocular Histoplasmosis Syndrome, DNA:polymorphisms:cds:HLA-B7 human | RGD | |
Meniere's disease | | ISO | RGD:1352836 | 7364921 | DNA:polymorphisms:cds:HLA-B44 human, South Korean | RGD | |
mitral valve prolapse | | ISO | RGD:1352836 | 7365110 | associated with Graves Disease, DNA:polymorphisms:cds:HLA-B15 human | RGD | |
Nasal Polyps | susceptibility | ISO | RGD:1352836 | 7364876 | DNA:polymorphisms:cds:HLA-B*07 more ... | RGD | |
otosclerosis | susceptibility | ISO | RGD:1352836 | 7364875 | DNA:polymorphisms:cds:HLA-B*35 more ... | RGD | |
reactive arthritis | | ISO | RGD:1352836 | 7365111 | DNA:polymorphisms:cds:HLA-B27 human | RGD | |
retinal vasculitis | | ISO | RGD:1352836 | 7364920 | associated with Behcet Syndrome, DNA:polymorphisms:cds HLA B-5 human | RGD | |
retinopathy of prematurity | | ISO | RGD:1352836 | 7365093 | DNA:polymorphisms:cds:HLA-B*38 human | RGD | |
sarcoidosis | susceptibility | ISO | RGD:1352836 | 7364872 | DNA:polymorphisms:cds:HLA-B-7, HLA-B-8 human | RGD | |
sensorineural hearing loss | | ISO | RGD:1352836 | 7365120 | Unilateral Childhood Sensorineural Hearing Loss, DNA:polymorphisms:cds:HLA-Bw54 human | RGD | |
spondyloarthropathy | | ISO | RGD:1352836 | 7387221 | DNA:polymorphisms:cds:HLA-B27 human | RGD | |
Stevens-Johnson syndrome | susceptibility | ISO | RGD:1352836 | 7365090 | DNA:polymorphisms:cds:HLA-B*15:02 more ... | RGD | |
Stevens-Johnson syndrome | | ISO | RGD:1352836 | 7364874 | DNA:polymorphisms:cds:HLA-B*5801 human, Japanese | RGD | |
thrombophlebitis | | ISO | RGD:1352836 | 7364924 | associated with Behcet Syndrome more ... | RGD | |
Thyrotoxic Periodic Paralysis | | ISO | RGD:1352836 | 8655904 | protein:increased expression:peripheral blood cell human | RGD | |
trachoma | | ISO | RGD:1352836 | 7364877 | DNA:polymorphisms:cds:HLA-B*14 human, Tanzanian | RGD | |
Transplant Rejection | treatment | ISO | RGD:1352836 | 7387273 | human peptide in rat model, HLA-B7 | RGD | |
Trichiasis | | ISO | RGD:1352836 | 7364877 | DNA:polymorphisms:cds HLA-B*07 more ... | RGD | |
uveal melanoma | severity | ISO | RGD:1352836 | 7364941 | protein:increased expression:tumor of uvea human | RGD | |
uveitis | treatment | ISO | RGD:1352836 | 7364942 | | RGD | |
uveitis | | ISO | RGD:1352836 | 7364926 | associated with Inflammatory Bowel Diseases more ... | RGD | |
uveitis | onset | ISO | RGD:1352836 | 7364788 | associated with Behcet Syndrome, DNA:polymorphisms:cds:HLA-B*51 human | RGD | |