MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Leukopenia
[NCBI]
Gene
Gene
Link
Information
Gain
01
MS
[NCBI]
0.000105673
TPMT
[NCBI]
7.11093e-05
TNF
[NCBI]
3.89887e-05
UGT1A1
[NCBI]
2.71877e-05
ITPA
[NCBI]
2.09999e-05
IL7
[NCBI]
1.6986e-05
DPYD
[NCBI]
1.64412e-05
TROVE2
[NCBI]
1.62189e-05
SPI1
[NCBI]
1.33706e-05
ABCC2
[NCBI]
1.2949e-05
ST3GAL3
[NCBI]
1.21146e-05
RRP9
[NCBI]
1.10479e-05
AOAH
[NCBI]
1.03958e-05
CYP3A4
[NCBI]
1.02022e-05
ABCB1
[NCBI]
9.56282e-06
GFI1
[NCBI]
9.44839e-06
SLCO1B3
[NCBI]
9.34748e-06
EPO
[NCBI]
8.97703e-06
UGT2B7
[NCBI]
8.91661e-06
MPO
[NCBI]
8.89429e-06
MTF1
[NCBI]
8.4525e-06
KIF11
[NCBI]
8.34016e-06
NR1I2
[NCBI]
8.23476e-06
FCER1A
[NCBI]
8.13549e-06
RRM2
[NCBI]
8.08794e-06
ADA
[NCBI]
7.99357e-06
MERTK
[NCBI]
7.95276e-06
SBDS
[NCBI]
7.74886e-06
INHA
[NCBI]
7.40231e-06
CALCA
[NCBI]
7.37808e-06
CLC
[NCBI]
7.31076e-06
HPRT1
[NCBI]
7.28131e-06
CYP2C8
[NCBI]
7.1959e-06
NR1I3
[NCBI]
6.96277e-06
CEBPA
[NCBI]
6.89167e-06
CD177
[NCBI]
6.63384e-06
MYH9
[NCBI]
6.59445e-06
PLAT
[NCBI]
6.37562e-06
CYP3A5
[NCBI]
5.67297e-06
TYMS
[NCBI]
5.34689e-06
TFRC
[NCBI]
5.04333e-06
CD46
[NCBI]
4.63001e-06
PARP1
[NCBI]
4.51444e-06
BTK
[NCBI]
4.16465e-06
IL4
[NCBI]
3.82595e-06
NAT2
[NCBI]
3.71047e-06
ADAMTS13
[NCBI]
3.63151e-06
RUNX1
[NCBI]
3.56863e-06
FLT3
[NCBI]
3.53812e-06
TLR2
[NCBI]
3.46724e-06
ACP5
[NCBI]
3.34787e-06
GSTP1
[NCBI]
2.70014e-06
TLR4
[NCBI]
2.40564e-06
MTHFR
[NCBI]
2.13125e-06
IL1RN
[NCBI]
1.87233e-06
NPY
[NCBI]
1.86951e-06
MBP
[NCBI]
1.82609e-06
TGFB1
[NCBI]
1.47463e-06
VWF
[NCBI]
1.38934e-06
FASLG
[NCBI]
1.34934e-06
OMIM
OMIM
Link
Information
gain
01
reticular dysgenesia
[NCBI]
0.00376137
neutropenia, chronic familial
[NCBI]
0.00214098
GHDD
[NCBI]
0.000711792
zinc, elevated plasma
[NCBI]
0.000672238
immune defect due to absence of thymus
[NCBI]
0.000572697
SLE
[NCBI]
0.000375979
TPMT
[NCBI]
0.000307786
SDS
[NCBI]
0.000139586
TNF
[NCBI]
0.00012358
myelolymphatic insufficiency
[NCBI]
0.000117198
COH1
[NCBI]
0.000103994
orotic aciduria i
[NCBI]
0.000100354
granulomatous disease with defect in neutrophil chemotaxis
[NCBI]
9.47367e-05
lazy leukocyte syndrome
[NCBI]
8.07696e-05
TYMS
[NCBI]
7.49095e-05
achondroplasia, so-called, and severe combined immunodeficiency
[NCBI]
7.07301e-05
FHL2
[NCBI]
7.07301e-05
lymphedema, hereditary, ii
[NCBI]
6.46048e-05
IFNA1
[NCBI]
5.93218e-05
cutis laxa, autosomal recessive, type ii
[NCBI]
5.67342e-05
omenn syndrome
[NCBI]
5.39002e-05
propionic acidemia
[NCBI]
5.22591e-05
AOAH
[NCBI]
5.07031e-05
CVID
[NCBI]
3.94506e-05
SCIDX1
[NCBI]
3.89509e-05
THPO
[NCBI]
3.65011e-05
CF
[NCBI]
3.59605e-05
LPI
[NCBI]
3.15638e-05
IL4
[NCBI]
3.04267e-05
giant platelet syndrome
[NCBI]
2.66919e-05
ABCB1
[NCBI]
2.62911e-05
ADA
[NCBI]
2.45873e-05
EPO
[NCBI]
2.16651e-05
MPO
[NCBI]
2.16548e-05
ABCC1
[NCBI]
1.58301e-05
VRNI
[NCBI]
1.40116e-05
RA
[NCBI]
1.21714e-05
XDH
[NCBI]
1.21398e-05
GIST
[NCBI]
1.13888e-05
VEGF
[NCBI]
5.00028e-06
FMF
[NCBI]
3.88636e-06
CD
[NCBI]
3.31871e-06
NPY
[NCBI]
2.23669e-06
MBP
[NCBI]
2.16627e-06
KLK3
[NCBI]
2.00981e-06
Database Center for Life Science