Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Cholestyramine Resin	[NCBI]

Gene	Link	Information Gain
AACSL	[NCBI]	0.000264782
CCK	[NCBI]	1.18533e-05
HDLBP	[NCBI]	5.08532e-06
NR1H3	[NCBI]	4.25947e-06
APOB	[NCBI]	3.94854e-06
LPL	[NCBI]	3.34773e-06
SCP2	[NCBI]	3.12691e-06
CETP	[NCBI]	2.33445e-06
HMGCS1	[NCBI]	2.27394e-06
PDSS1	[NCBI]	2.24959e-06
CYP7B1	[NCBI]	1.93331e-06
FGF19	[NCBI]	1.88753e-06
CYP7A1	[NCBI]	1.81898e-06
HMGCR	[NCBI]	1.81436e-06
NR1H4	[NCBI]	1.78414e-06
PCSK9	[NCBI]	1.58586e-06
AKR1C2	[NCBI]	1.49873e-06
SREBF2	[NCBI]	1.47332e-06
LCAT	[NCBI]	1.4288e-06
CYP27A1	[NCBI]	1.41105e-06
MLX	[NCBI]	1.36229e-06
HNF4A	[NCBI]	1.34362e-06
APOA1	[NCBI]	1.31188e-06
BMP2	[NCBI]	9.43915e-07
APOE	[NCBI]	7.18685e-07
PCNA	[NCBI]	6.98779e-07
TNF	[NCBI]	3.91349e-07

OMIM	Link	Information gain
nephrolithiasis, calcium oxalate	[NCBI]	0.0022261
BRIC1	[NCBI]	0.000284534
sitosterolemia	[NCBI]	0.000236607
hypercholesterolemia, autosomal dominant	[NCBI]	0.000163133
CCK	[NCBI]	0.000117405
crigler-najjar syndrome	[NCBI]	0.000103444
hyperlipoproteinemia, type i	[NCBI]	0.000102248
porphyria, congenital erythropoietic	[NCBI]	0.000100032
PFIC1	[NCBI]	9.61622e-05
cerebrotendinous xanthomatosis	[NCBI]	9.52902e-05
APOB	[NCBI]	4.02362e-05
HMGCS1	[NCBI]	3.51417e-05
FGF19	[NCBI]	3.16762e-05
LPL	[NCBI]	2.75944e-05
NR1H4	[NCBI]	2.53161e-05
wolman disease	[NCBI]	2.37236e-05
protoporphyria, erythropoietic	[NCBI]	2.30767e-05
MMP9	[NCBI]	2.21479e-05
NR0B2	[NCBI]	2.10725e-05
LCAT	[NCBI]	1.1574e-05
APOE	[NCBI]	3.53588e-06
PCNA	[NCBI]	2.06337e-06
RA	[NCBI]	1.40451e-06
TNF	[NCBI]	1.40546e-08
VEGF	[NCBI]	1.73192e-10