MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Hyperbilirubinemia
[NCBI]
Gene
Gene
Link
Information
Gain
01
UGT1A11P
[NCBI]
0.000438875
UGT1A2P
[NCBI]
0.000438875
UGT1A13P
[NCBI]
0.000438875
UGT1A12P
[NCBI]
0.000378131
UGT1A1
[NCBI]
0.000321027
UGT1A@
[NCBI]
0.000313087
HBB@
[NCBI]
0.000239942
ABCC2
[NCBI]
0.000182907
G6PD
[NCBI]
8.93042e-05
SLCO1B1
[NCBI]
4.39199e-05
NR1I3
[NCBI]
3.63745e-05
UGT1A9
[NCBI]
2.93388e-05
SLCO1B3
[NCBI]
2.05781e-05
ATP8B1
[NCBI]
1.71631e-05
ADAMTS13
[NCBI]
1.55533e-05
HGF
[NCBI]
1.48501e-05
UGT1A5
[NCBI]
1.32889e-05
SLC22A7
[NCBI]
1.23906e-05
UGT1A3
[NCBI]
1.18073e-05
TBC1D9
[NCBI]
1.18073e-05
SLCO2A1
[NCBI]
1.18073e-05
UGT1A8
[NCBI]
1.13736e-05
UGT1A10
[NCBI]
1.1028e-05
RDX
[NCBI]
1.02797e-05
UGT1A4
[NCBI]
1.02797e-05
PHF6
[NCBI]
1.00886e-05
VPS33B
[NCBI]
9.76069e-06
ABCC3
[NCBI]
9.14142e-06
HPX
[NCBI]
8.85505e-06
OTX2
[NCBI]
8.60983e-06
UGT1A6
[NCBI]
8.39543e-06
UGT1A7
[NCBI]
8.03365e-06
HESX1
[NCBI]
7.69035e-06
AKR1C2
[NCBI]
7.12812e-06
S100B
[NCBI]
6.91827e-06
GPI
[NCBI]
6.54072e-06
ABCC6
[NCBI]
5.92418e-06
FABP7
[NCBI]
4.54751e-06
MEFV
[NCBI]
4.0428e-06
HNF1A
[NCBI]
3.79018e-06
ALB
[NCBI]
3.73184e-06
PIH
[NCBI]
3.68748e-06
ABCB1
[NCBI]
3.32703e-06
MAPT
[NCBI]
3.16287e-06
CST3
[NCBI]
2.60951e-06
PTHLH
[NCBI]
2.47254e-06
ACHE
[NCBI]
1.90047e-06
LPL
[NCBI]
1.88331e-06
NOS2
[NCBI]
1.5903e-06
GFAP
[NCBI]
1.15043e-06
VWF
[NCBI]
1.14924e-06
EPO
[NCBI]
1.08745e-06
PCNA
[NCBI]
8.88248e-07
OMIM
OMIM
Link
Information
gain
01
CDAN2
[NCBI]
0.00139914
cholestasis-lymphedema syndrome
[NCBI]
0.000773718
ABCC2
[NCBI]
0.000756638
red cell phospholipid defect with hemolysis
[NCBI]
0.00074746
DJS
[NCBI]
0.000506586
G6PD
[NCBI]
0.00046263
hyperbilirubinemia, transient familial neonatal
[NCBI]
0.000440442
klippel-trenaunay-weber syndrome
[NCBI]
0.000368517
UGT1A1
[NCBI]
0.000354984
PFIC1
[NCBI]
0.000328811
gilbert syndrome
[NCBI]
0.000254783
crigler-najjar syndrome
[NCBI]
0.000248144
hyperbilirubinemia, conjugated, type iii
[NCBI]
0.000131618
bilirubin, elevated concentrations of, in serum
[NCBI]
0.000100673
RHN
[NCBI]
9.1078e-05
mevalonic aciduria
[NCBI]
8.78187e-05
crigler-najjar syndrome, type ii
[NCBI]
7.58729e-05
IHPS1
[NCBI]
7.21276e-05
RDX
[NCBI]
5.92489e-05
ABCC3
[NCBI]
4.97082e-05
HBB
[NCBI]
4.9176e-05
ATP8B1
[NCBI]
4.40488e-05
NDP
[NCBI]
3.29314e-05
LIPC
[NCBI]
2.89219e-05
NR1I2
[NCBI]
2.68085e-05
HGF
[NCBI]
2.51213e-05
ABCB1
[NCBI]
2.39424e-05
LCAT
[NCBI]
1.49919e-05
ABCC1
[NCBI]
1.36305e-05
PTHLH
[NCBI]
8.31854e-06
TYMS
[NCBI]
4.68839e-06
MG
[NCBI]
3.7199e-06
LPL
[NCBI]
2.35667e-06
ACHE
[NCBI]
1.97777e-06
CRC
[NCBI]
1.94813e-06
GFAP
[NCBI]
1.4875e-07
EPO
[NCBI]
9.05741e-08
PCNA
[NCBI]
1.53558e-09
Database Center for Life Science