Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Jaundice	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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