Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Lymphocytosis [NCBI]

Gene


 Gene Link Information
Gain		 01
AGS2 [NCBI] 0.000329245
TEC [NCBI] 0.000191188
MS [NCBI] 4.22463e-05
TREX1 [NCBI] 3.90933e-05
RNASEH2A [NCBI] 2.6693e-05
CD38 [NCBI] 2.06532e-05
TIA1 [NCBI] 1.73675e-05
CCL17 [NCBI] 1.6603e-05
RNASEH2C [NCBI] 1.43341e-05
FAS [NCBI] 1.33063e-05
CD69 [NCBI] 1.14278e-05
MAP3K8 [NCBI] 1.05509e-05
IL8RA [NCBI] 9.30562e-06
KLRC1 [NCBI] 8.74479e-06
PIM1 [NCBI] 8.64171e-06
TCL1A [NCBI] 8.54449e-06
KLRD1 [NCBI] 8.26204e-06
FASLG [NCBI] 7.83852e-06
IL12B [NCBI] 7.63284e-06
TNF [NCBI] 7.48541e-06
CXCL9 [NCBI] 7.07187e-06
CD52 [NCBI] 7.06194e-06
KLRK1 [NCBI] 6.88364e-06
CXCL10 [NCBI] 6.75503e-06
CCL5 [NCBI] 6.39231e-06
CTLA4 [NCBI] 5.89922e-06
IL1A [NCBI] 5.88931e-06
ATR [NCBI] 5.83583e-06
WAS [NCBI] 5.67188e-06
CCR5 [NCBI] 5.51073e-06
IFNG [NCBI] 5.44508e-06
MUC1 [NCBI] 5.18614e-06
IL10 [NCBI] 4.19162e-06
BCL2L1 [NCBI] 3.77915e-06



OMIM


 OMIM Link Information
gain		 01
hemophagocytic lymphohistiocytosis, familial, 1 [NCBI] 0.00299509
AGS1 [NCBI] 0.00071874
basal ganglia calcification, idiopathic, childhood-onset [NCBI] 0.000672238
persistent polyclonal b-cell lymphocytosis [NCBI] 0.000530316
AGS2 [NCBI] 0.00010915
CHBL [NCBI] 9.51693e-05
RNASEH2B [NCBI] 8.00936e-05
RNASEH2C [NCBI] 8.00936e-05
RNASEH2A [NCBI] 7.48929e-05
CYR61 [NCBI] 6.90048e-05
CVID [NCBI] 6.62958e-05
TREX1 [NCBI] 6.15648e-05
TCL1A [NCBI] 5.80724e-05
LIP [NCBI] 5.55972e-05
TNFSF6 [NCBI] 4.77362e-05
CSF3 [NCBI] 4.55901e-05
lymphoma, non-hodgkin, familial [NCBI] 4.12419e-05
ACP5 [NCBI] 2.5006e-05
WAS [NCBI] 2.40985e-05
TNFRSF11B [NCBI] 2.05383e-05
temporal arteritis [NCBI] 1.80624e-05
CD [NCBI] 1.30748e-05
TNF [NCBI] 1.17928e-05
VEGF [NCBI] 1.0104e-05
MG [NCBI] 3.7199e-06
SLE [NCBI] 1.76805e-07
RA [NCBI] 1.48406e-07



Database Center for Life Science