MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Jaundice
[NCBI]
Gene
Gene
Link
Information
Gain
01
UGT1A1
[NCBI]
5.67e-05
G6PD
[NCBI]
3.68276e-05
ABCC2
[NCBI]
1.66143e-05
IL25
[NCBI]
1.1744e-05
INVS
[NCBI]
1.07349e-05
HFE
[NCBI]
1.01377e-05
HLA-DRB5
[NCBI]
9.64377e-06
HGF
[NCBI]
9.24349e-06
NR1I3
[NCBI]
8.77615e-06
AFP
[NCBI]
8.01574e-06
SELE
[NCBI]
7.52422e-06
TIMP1
[NCBI]
7.45561e-06
PLG
[NCBI]
7.32618e-06
TFRC
[NCBI]
6.84159e-06
HBB
[NCBI]
6.64296e-06
CXCL1
[NCBI]
6.33885e-06
HLA-DQA1
[NCBI]
5.9706e-06
ADAMTS13
[NCBI]
5.39991e-06
ACP5
[NCBI]
5.10635e-06
HLA-DQB1
[NCBI]
4.72657e-06
HLA-DRB1
[NCBI]
4.1138e-06
IL1RN
[NCBI]
3.53288e-06
VWF
[NCBI]
2.98536e-06
TNF
[NCBI]
1.02345e-06
OMIM
OMIM
Link
Information
gain
01
hyperbilirubinemia, rotor type
[NCBI]
0.000898321
red cell phospholipid defect with hemolysis
[NCBI]
0.000840405
iminoglycinuria
[NCBI]
0.00078076
ICP
[NCBI]
0.000382665
HBB
[NCBI]
0.000240237
G6PD
[NCBI]
0.000238345
PFIC1
[NCBI]
0.000232871
DJS
[NCBI]
0.000216971
crigler-najjar syndrome
[NCBI]
0.000152257
UGT1A1
[NCBI]
0.000135572
dysmyelination with jaundice
[NCBI]
0.000132242
heinz body anemias
[NCBI]
0.000109774
CEACAM5
[NCBI]
9.65337e-05
beta thalassemia, dominant inclusion body type
[NCBI]
9.17009e-05
hyperpipecolatemia
[NCBI]
8.34124e-05
cystathioninuria
[NCBI]
7.51466e-05
IHPS1
[NCBI]
7.27487e-05
septooptic dysplasia
[NCBI]
6.97129e-05
SPTAN1
[NCBI]
6.80811e-05
gilbert syndrome
[NCBI]
6.63934e-05
sickle cell anemia
[NCBI]
5.08891e-05
NOS2A
[NCBI]
4.29619e-05
SPTB
[NCBI]
4.14755e-05
AK1
[NCBI]
4.14755e-05
ALPS
[NCBI]
4.09893e-05
wilson disease
[NCBI]
4.02615e-05
PKLR
[NCBI]
3.77044e-05
fructose intolerance, hereditary
[NCBI]
3.59867e-05
coproporphyria
[NCBI]
3.57276e-05
SPTA1
[NCBI]
3.17895e-05
HS
[NCBI]
3.06657e-05
HBA1
[NCBI]
2.36141e-05
PLG
[NCBI]
2.28557e-05
SLE
[NCBI]
1.75524e-05
HGF
[NCBI]
1.60264e-05
RA
[NCBI]
1.23195e-05
lymphoma, non-hodgkin, familial
[NCBI]
1.14933e-05
AFP
[NCBI]
9.66565e-06
TNF
[NCBI]
2.37119e-06
Database Center for Life Science