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01 Cholestyramine Resin [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science