Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Lymphadenitis	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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