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MeSH keywords -> Related genes, diseases (OMIM)


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01 Lymphadenitis [NCBI]


Gene


Gene Link Information
Gain
01
CD68 [NCBI] 2.32923e-05
CCL19 [NCBI] 1.94652e-05
CCR7 [NCBI] 1.49606e-05
SEMA6A [NCBI] 1.36381e-05
FCRL4 [NCBI] 1.25711e-05
IFNGR1 [NCBI] 1.23594e-05
NOD2 [NCBI] 1.15806e-05
CD207 [NCBI] 9.86102e-06
DEK [NCBI] 9.60834e-06
PAX4 [NCBI] 9.60834e-06
SIGLEC1 [NCBI] 9.43001e-06
CLC [NCBI] 8.82923e-06
BNIP3 [NCBI] 8.48004e-06
RELB [NCBI] 8.38553e-06
IKBKG [NCBI] 8.12983e-06
EBAG9 [NCBI] 7.89023e-06
CCL21 [NCBI] 7.8228e-06
FASLG [NCBI] 7.61864e-06
CCL22 [NCBI] 7.50691e-06
CX3CL1 [NCBI] 7.36222e-06
TIA1 [NCBI] 7.34966e-06
CTAGE1 [NCBI] 7.32481e-06
CCR4 [NCBI] 6.83527e-06
CD83 [NCBI] 6.65981e-06
MEFV [NCBI] 5.83325e-06
RAG1 [NCBI] 5.56083e-06
GZMB [NCBI] 5.47633e-06
TF [NCBI] 5.42361e-06
FAS [NCBI] 5.33426e-06
CD86 [NCBI] 5.1083e-06
CALCA [NCBI] 3.99723e-06
HRAS [NCBI] 3.75787e-06
TGFB1 [NCBI] 2.80836e-06
PRL [NCBI] 2.42045e-06
CASP3 [NCBI] 2.16728e-06
TNF [NCBI] 8.12137e-07




OMIM


OMIM Link Information
gain
01
SLE [NCBI] 0.00034212
CGD [NCBI] 0.000180854
immunodeficiency without anhidrotic ectodermal dysplasia [NCBI] 9.83952e-05
whim syndrome [NCBI] 8.28342e-05
ITPKC [NCBI] 7.48929e-05
kawasaki disease [NCBI] 6.87826e-05
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant [NCBI] 6.0147e-05
CEACAM6 [NCBI] 5.96656e-05
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i [NCBI] 5.73722e-05
periodic fever, familial, autosomal dominant [NCBI] 5.50112e-05
IKBKG [NCBI] 5.06541e-05
CYBB [NCBI] 5.06541e-05
TNFRSF6 [NCBI] 4.87592e-05
BCL2 [NCBI] 4.51816e-05
ALPS [NCBI] 3.81822e-05
PI [NCBI] 2.86475e-05
TF [NCBI] 2.52334e-05
SPP1 [NCBI] 2.05691e-05
RA [NCBI] 2.03048e-05
G6PD [NCBI] 1.60252e-05
lymphoma, non-hodgkin, familial [NCBI] 9.31249e-06
PRL [NCBI] 7.42263e-06
CEACAM5 [NCBI] 4.44268e-06
TNF [NCBI] 1.43151e-06




Database Center for Life Science