MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Hyperlipoproteinemias
[NCBI]
Gene
Gene
Link
Information
Gain
01
CETP
[NCBI]
0.000509079
LPL
[NCBI]
0.000252171
APOB
[NCBI]
4.7364e-05
APOE
[NCBI]
4.40831e-05
PLTP
[NCBI]
2.14957e-05
APOA5
[NCBI]
2.04846e-05
LCAT
[NCBI]
1.2399e-05
LBP
[NCBI]
9.86947e-06
ANGPTL3
[NCBI]
9.36134e-06
APOC1
[NCBI]
7.1818e-06
LRP5
[NCBI]
6.54417e-06
HDLBP
[NCBI]
6.18016e-06
FABP1
[NCBI]
6.15516e-06
LIPC
[NCBI]
5.31457e-06
OLR1
[NCBI]
5.1035e-06
APOC3
[NCBI]
5.06434e-06
TNFRSF1B
[NCBI]
4.7698e-06
SREBF1
[NCBI]
4.52024e-06
PF4
[NCBI]
3.34752e-06
CRP
[NCBI]
3.34311e-06
PIH
[NCBI]
3.16076e-06
PLAUR
[NCBI]
1.83089e-06
CAT
[NCBI]
1.52718e-06
CD68
[NCBI]
1.31071e-06
OMIM
OMIM
Link
Information
gain
01
chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase
[NCBI]
0.00159179
LPL
[NCBI]
0.00112822
cholesteryl ester transfer protein deficiency
[NCBI]
0.00024142
APOE
[NCBI]
0.000225312
LIPC
[NCBI]
0.000213865
hyperalphalipoproteinemia
[NCBI]
0.000199466
apolipoprotein c-ii deficiency
[NCBI]
0.000195114
APOB
[NCBI]
0.000193469
LCAT
[NCBI]
0.000179432
hyperlipoproteinemia, type i
[NCBI]
0.000170641
LPG
[NCBI]
0.000168789
FED
[NCBI]
0.000160853
CETP
[NCBI]
0.00014657
hypertriglyceridemia, familial
[NCBI]
8.69446e-05
lipomatosis, familial benign cervical
[NCBI]
8.00231e-05
APOA1
[NCBI]
6.72462e-05
homocysteinemia
[NCBI]
6.48133e-05
FCHL
[NCBI]
6.32541e-05
TGD
[NCBI]
6.22932e-05
CDG1A
[NCBI]
5.68226e-05
APOC3
[NCBI]
4.56389e-05
hypercholesterolemia, autosomal dominant
[NCBI]
4.50442e-05
APOC2
[NCBI]
3.91147e-05
LBP
[NCBI]
2.43749e-05
PLTP
[NCBI]
2.01984e-05
LRP1
[NCBI]
1.85092e-05
PF4
[NCBI]
9.08564e-06
PPARA
[NCBI]
5.50696e-06
CAT
[NCBI]
1.26777e-06
SLE
[NCBI]
7.8177e-07
Database Center for Life Science