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MeSH keywords -> Related genes, diseases (OMIM)


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01 Gout [NCBI]

Gene


 Gene Link Information
Gain		 01
GOUT1 [NCBI] 0.000499621
SLC22A12 [NCBI] 0.000184849
HPRT1 [NCBI] 0.000113793
UMOD [NCBI] 7.75322e-05
SLC2A9 [NCBI] 6.90471e-05
APRT [NCBI] 6.58826e-05
NLRP3 [NCBI] 4.20423e-05
PRPS1 [NCBI] 2.32083e-05
MYD88 [NCBI] 1.36307e-05
SLC17A3 [NCBI] 1.26105e-05
PRPS2 [NCBI] 1.26105e-05
ZNF365 [NCBI] 1.20271e-05
SLC22A6 [NCBI] 1.20271e-05
TEC [NCBI] 8.2529e-06
IL1B [NCBI] 8.04847e-06
XDH [NCBI] 7.02758e-06
IL1R1 [NCBI] 6.48829e-06
PTH [NCBI] 6.17878e-06
TREM1 [NCBI] 6.11065e-06
APOA1 [NCBI] 5.12768e-06
CXCL1 [NCBI] 4.46314e-06
IKBKE [NCBI] 4.44055e-06
CHUK [NCBI] 4.27035e-06
IKBKB [NCBI] 4.26029e-06
PRKCA [NCBI] 4.19636e-06
HNF1B [NCBI] 4.14419e-06
ABCG2 [NCBI] 4.12102e-06
CYP3A4 [NCBI] 3.847e-06
IL4 [NCBI] 3.74214e-06
PKD1 [NCBI] 3.72772e-06
CTSL1 [NCBI] 3.56748e-06
TLR2 [NCBI] 3.38434e-06
ACP5 [NCBI] 3.26531e-06
TNFRSF11A [NCBI] 3.13523e-06
TNF [NCBI] 3.0707e-06
NOD2 [NCBI] 3.05203e-06
PTGS2 [NCBI] 2.91836e-06
PTGS1 [NCBI] 2.91725e-06
TNFSF11 [NCBI] 2.91093e-06
TNFRSF11B [NCBI] 2.8715e-06
ADA [NCBI] 2.77828e-06
VIP [NCBI] 2.55114e-06
PLAUR [NCBI] 2.51549e-06
STAT3 [NCBI] 2.17763e-06
LPL [NCBI] 2.07404e-06
IL1RN [NCBI] 1.79761e-06
AKT1 [NCBI] 1.68951e-06
TGFB1 [NCBI] 1.404e-06
CDKN1A [NCBI] 7.44732e-07



OMIM


 OMIM Link Information
gain		 01
gout susceptibility 1 [NCBI] 0.00804012
HNFJ [NCBI] 0.00119227
HPRT1 [NCBI] 0.00115885
urate-binding globulin, decrease in [NCBI] 0.00108068
phosphoribosylpyrophosphate synthetase superactivity [NCBI] 0.00104809
MCKD1 [NCBI] 0.000467507
CDAN2 [NCBI] 0.000451673
RA [NCBI] 0.000407358
gout, hprt-related [NCBI] 0.000353863
APRT [NCBI] 0.000349827
LNS [NCBI] 0.000199136
glycogen storage disease i [NCBI] 0.000178747
hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase [NCBI] 0.000110667
MCKD2 [NCBI] 5.99137e-05
lipomatosis, familial benign cervical [NCBI] 5.50618e-05
renal cysts and diabetes syndrome [NCBI] 5.37269e-05
PRPS1 [NCBI] 5.07031e-05
xanthinuria, type i [NCBI] 5.02908e-05
NLRP3 [NCBI] 4.64616e-05
CCAL2 [NCBI] 4.01014e-05
HNF1B [NCBI] 3.98198e-05
bartter syndrome, type 3 [NCBI] 3.90729e-05
FPLD2 [NCBI] 3.811e-05
hypophosphatasia, infantile [NCBI] 3.6772e-05
SPDA1 [NCBI] 3.63514e-05
GSR [NCBI] 3.5895e-05
FMF [NCBI] 3.47925e-05
UMOD [NCBI] 3.47855e-05
LIPC [NCBI] 3.13002e-05
ARMD1 [NCBI] 2.80323e-05
PSORS1 [NCBI] 2.45376e-05
XDH [NCBI] 1.21398e-05
PTH [NCBI] 1.03178e-05
TNFRSF11B [NCBI] 8.66346e-06
ADA [NCBI] 6.50876e-06
CVID [NCBI] 5.84179e-06
VIP [NCBI] 5.35655e-06
LPL [NCBI] 3.79107e-06
TNF [NCBI] 3.5565e-06
SLE [NCBI] 8.83462e-08



Database Center for Life Science