MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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