Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Allopurinol [NCBI]

Gene


 Gene Link Information
Gain		 01
XDH [NCBI] 3.20541e-05
CAT [NCBI] 2.10508e-05
MPO [NCBI] 1.98187e-05
APRT [NCBI] 1.96283e-05
MOCOS [NCBI] 4.51853e-06
HMOX1 [NCBI] 3.376e-06
HPRT1 [NCBI] 3.15026e-06
GSTA5 [NCBI] 2.91822e-06
CASP3 [NCBI] 2.78724e-06
NOS3 [NCBI] 2.58433e-06
ICAM1 [NCBI] 2.33988e-06
PTH [NCBI] 1.81274e-06
TMBIM6 [NCBI] 1.75154e-06
POU3F1 [NCBI] 1.61293e-06
NOS2 [NCBI] 1.48278e-06
OTC [NCBI] 1.43532e-06
SLC22A12 [NCBI] 1.42325e-06
ABCC4 [NCBI] 1.39526e-06
CD247 [NCBI] 1.33809e-06
RPGR [NCBI] 1.32553e-06
VIP [NCBI] 1.28379e-06
TPMT [NCBI] 1.23029e-06
CYSLTR2 [NCBI] 1.20314e-06
OLR1 [NCBI] 1.17734e-06
CYSLTR1 [NCBI] 1.07716e-06
MBL2 [NCBI] 1.05859e-06
DDIT3 [NCBI] 1.05859e-06
HLA-C [NCBI] 1.01087e-06
BAD [NCBI] 9.81964e-07
MAPK14 [NCBI] 9.64672e-07
SELPLG [NCBI] 9.58471e-07
SRC [NCBI] 9.41658e-07
CD46 [NCBI] 9.00937e-07
PDGFA [NCBI] 8.86586e-07
MCL1 [NCBI] 8.82354e-07
NAT2 [NCBI] 8.78189e-07
UMOD [NCBI] 8.75946e-07
MMP9 [NCBI] 8.74461e-07
HLA-A [NCBI] 8.59709e-07
PTPN11 [NCBI] 8.24444e-07
HLA-B [NCBI] 8.08178e-07
CTGF [NCBI] 7.96412e-07
NFKB1 [NCBI] 7.93417e-07
PLN [NCBI] 7.50863e-07
PTHLH [NCBI] 7.36378e-07
ADA [NCBI] 7.07145e-07
HLA-DRB1 [NCBI] 6.98414e-07
IL6 [NCBI] 6.42888e-07
TNF [NCBI] 6.26148e-07
TNFSF10 [NCBI] 6.20858e-07
BCL2L1 [NCBI] 6.02908e-07
IL1RN [NCBI] 5.81698e-07
BAX [NCBI] 4.93205e-07
VWF [NCBI] 4.72044e-07
AVP [NCBI] 4.64561e-07
CCK [NCBI] 4.43529e-07
ACHE [NCBI] 4.01051e-07
EGF [NCBI] 1.90105e-07



OMIM


 OMIM Link Information
gain		 01
XDH [NCBI] 0.00320212
poland syndrome [NCBI] 0.00277021
LNS [NCBI] 0.000534343
phosphoribosylpyrophosphate synthetase superactivity [NCBI] 0.000346581
APRT [NCBI] 0.000295061
severe cutaneous adverse reaction, susceptibility to [NCBI] 0.000254432
HNFJ [NCBI] 0.000202522
hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase [NCBI] 0.000180991
CAT [NCBI] 0.000123946
gout, hprt-related [NCBI] 0.00011236
MPO [NCBI] 0.000101352
xanthinuria, type i [NCBI] 9.445e-05
uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to [NCBI] 9.06659e-05
UOX [NCBI] 8.84563e-05
molybdenum cofactor deficiency [NCBI] 8.64449e-05
hyperoxaluria, primary, type i [NCBI] 7.91265e-05
lymphoma, non-hodgkin, familial [NCBI] 7.11158e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 5.93945e-05
RA [NCBI] 4.36477e-05
HPRT1 [NCBI] 4.10426e-05
BL [NCBI] 4.06468e-05
EGF [NCBI] 2.68775e-05
SLE [NCBI] 2.37714e-05
MOCS1 [NCBI] 2.34962e-05
AGXT [NCBI] 1.85411e-05
TNF [NCBI] 1.73105e-05
HLA-B [NCBI] 1.48124e-05
RPGR [NCBI] 1.18345e-05
TPMT [NCBI] 8.08732e-06
MCP [NCBI] 6.14711e-06
ACHE [NCBI] 5.43939e-06
AVP [NCBI] 4.78706e-06
KLK3 [NCBI] 4.63403e-06
CCK [NCBI] 3.7105e-06
MBL2 [NCBI] 3.41535e-06
GJA1 [NCBI] 3.2706e-06
CTGF [NCBI] 1.65654e-06
PTH [NCBI] 1.00843e-06
SPP1 [NCBI] 2.69424e-07
VIP [NCBI] 2.40108e-07
PPARA [NCBI] 2.38807e-07
ADA [NCBI] 1.08233e-08



Database Center for Life Science