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MeSH keywords -> Related genes, diseases (OMIM)


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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