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MeSH keywords -> Related genes, diseases (OMIM)


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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