Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Mononuclear Phagocyte System	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	8.69867e-05
TNF	[NCBI]	1.73418e-05
SLC40A1	[NCBI]	1.45124e-05
SLC11A1	[NCBI]	1.04802e-05
ALB	[NCBI]	1.01595e-05
HFE	[NCBI]	9.95023e-06
C9	[NCBI]	7.98397e-06
CFP	[NCBI]	7.05445e-06
C4B	[NCBI]	6.80804e-06
HEPH	[NCBI]	6.55245e-06
C5	[NCBI]	6.47126e-06
EPO	[NCBI]	6.16503e-06
TFR2	[NCBI]	5.93953e-06
FCGR2B	[NCBI]	5.72092e-06
C3	[NCBI]	5.673e-06
TF	[NCBI]	3.68978e-06
HMOX1	[NCBI]	3.65543e-06
ACP5	[NCBI]	3.28125e-06
AFP	[NCBI]	2.89873e-06
CD68	[NCBI]	2.86547e-06

OMIM	Link	Information gain
hemophagocytic lymphohistiocytosis, familial, 1	[NCBI]	0.00120792
thrombocytopenic purpura, autoimmune	[NCBI]	0.000566081
TGD	[NCBI]	0.000529904
hemosiderosis, pulmonary, with deficiency of gamma-a globulin	[NCBI]	0.000202202
glycoprotein storage disease	[NCBI]	0.000202202
SLE	[NCBI]	0.00020193
HFE4	[NCBI]	0.000131402
SLC40A1	[NCBI]	0.000128838
nephrosialidosis	[NCBI]	0.000120998
mast cell disease	[NCBI]	0.000116959
aceruloplasminemia	[NCBI]	0.000110298
niemann-pick disease, type a	[NCBI]	9.31581e-05
atypical mycobacteriosis, familial	[NCBI]	9.0136e-05
WAS	[NCBI]	8.45568e-05
wolman disease	[NCBI]	7.30933e-05
neuraminidase deficiency	[NCBI]	6.38639e-05
TNF	[NCBI]	4.61011e-05
ALB	[NCBI]	4.58962e-05
HEPH	[NCBI]	3.85669e-05
SMPD1	[NCBI]	3.69163e-05
HS	[NCBI]	3.09935e-05
GUSB	[NCBI]	2.55342e-05
CF	[NCBI]	2.37442e-05
CP	[NCBI]	1.99e-05
ALD	[NCBI]	1.81465e-05
EPO	[NCBI]	1.71116e-05
TLR4	[NCBI]	1.41048e-05
TF	[NCBI]	1.29095e-05
XDH	[NCBI]	1.2387e-05
RA	[NCBI]	9.27738e-06
AFP	[NCBI]	7.40722e-06
CEACAM5	[NCBI]	5.49988e-06
MG	[NCBI]	1.91494e-06