Human | GRDX | 117189 | Graves disease, susceptibility to, X-linked | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | SCGB3A2 | 117156 | secretoglobin, family 3A, member 2 | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | FCRL3 | 115352 | Fc receptor-like 3 | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | IFIH1 | 64135 | interferon induced with helicase C domain 1 | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | RETN | 56729 | resistin | although resistin concentrations are increased in hyperthyroidism, they are not associated with body weight, body fat, waist circumference or body mass index |
Human | UACA | 55075 | uveal autoantigen with coiled-coil domains and ankyrin repeats | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | GRD2 | 50976 | Graves disease, susceptibility to, 2 | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | CD274 | 29126 | CD274 molecule | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | PTPN22 | 26191 | protein tyrosine phosphatase, non-receptor type 22 (lymphoid) | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | PRDX5 | 25824 | peroxiredoxin 5 | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | CXCR6 | 10663 | chemokine (C-X-C motif) receptor 6 | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | ADIPOQ | 9370 | adiponectin, C1Q and collagen domain containing | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | PAX8 | 7849 | paired box 8 | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | VDR | 7421 | vitamin D (1,25- dihydroxyvitamin D3) receptor | Title:Association of the vitamin D receptor genotype BB with low bone density in hyperthyroidism.|Association:Y|Conclusion:Not Found |
Human | TNFRSF4 | 7293 | tumor necrosis factor receptor superfamily, member 4 | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | TSHR | 7253 | thyroid stimulating hormone receptor | TSHR mutation as a sporadic germline mutation in a patient with hyperthyroidism after thyroid surgery an activating mutation in transmembrane helix 6 of the thyrotropin receptor plays a key role in the development of hereditary hyperthyroidism shed A subunits induce or amplify the immune response leading to hyperthyroidism and provide new insight into the etiology of Graves disease |
Human | TPO | 7173 | thyroid peroxidase | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | TNFRSF1B | 7133 | tumor necrosis factor receptor superfamily, member 1B | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | TNF | 7124 | tumor necrosis factor | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | THY1 | 7070 | Thy-1 cell surface antigen | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | THRB | 7068 | thyroid hormone receptor, beta | |
Human | TGFB1 | 7040 | transforming growth factor, beta 1 | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | TG | 7038 | thyroglobulin | study showed Taiwanese patients with the C/C genotype of E33SNP, smoking, ophthalmopathy & positive TSH-receptor antibodies at the end of the treatment were more likely to have a relapse of Graves' hyperthyroidism after antithyroid medication is withdrawn |
Human | TAP2 | 6891 | transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) | INFERRED, Score=800, UMLKSK CUI: C0020550 |
Human | TAP1 | 6890 | transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) | INFERRED, Score=800, UMLKSK CUI: C0020550 |