|
OMIM |
Link |
Information gain |
01 |
|
pentosuria
|
[NCBI]
|
0.00240735
|
|
|
crigler-najjar syndrome
|
[NCBI]
|
0.000521738
|
|
|
hyperbilirubinemia, transient familial neonatal
|
[NCBI]
|
0.000282701
|
|
|
sialuria, finnish type
|
[NCBI]
|
0.000209183
|
|
|
infantile sialic acid storage disorder
|
[NCBI]
|
0.000209183
|
|
|
fever, familial lifelong persistent
|
[NCBI]
|
0.000184253
|
|
|
acetophenetidin sensitivity
|
[NCBI]
|
0.000152669
|
|
|
AEXS
|
[NCBI]
|
0.000118873
|
|
|
hypoascorbemia
|
[NCBI]
|
0.000102248
|
|
|
gilbert syndrome
|
[NCBI]
|
9.3907e-05
|
|
|
mucopolysaccharidosis type iiia
|
[NCBI]
|
9.16952e-05
|
|
|
OCP
|
[NCBI]
|
6.80172e-05
|
|
|
CYP1A1
|
[NCBI]
|
4.69141e-05
|
|
|
UST
|
[NCBI]
|
4.15969e-05
|
|
|
CRC
|
[NCBI]
|
4.01751e-05
|
|
|
SLCO1B1
|
[NCBI]
|
3.5624e-05
|
|
|
UGT2B17
|
[NCBI]
|
3.36502e-05
|
|
|
RA
|
[NCBI]
|
3.35445e-05
|
|
|
SLC17A5
|
[NCBI]
|
3.01479e-05
|
|
|
MAG
|
[NCBI]
|
2.89948e-05
|
|
|
ABCC3
|
[NCBI]
|
2.7005e-05
|
|
|
SLC22A6
|
[NCBI]
|
2.5208e-05
|
|
|
DCN
|
[NCBI]
|
2.50412e-05
|
|
|
COMT
|
[NCBI]
|
2.37828e-05
|
|
|
UGT1A1
|
[NCBI]
|
2.09914e-05
|
|
|
ABCC2
|
[NCBI]
|
1.85312e-05
|
|
|
SLE
|
[NCBI]
|
1.72779e-05
|
|
|
FGF2
|
[NCBI]
|
1.65601e-05
|
|
|
PNMT
|
[NCBI]
|
1.25575e-05
|
|
|
ABCC1
|
[NCBI]
|
1.1028e-05
|
|
|
CEACAM5
|
[NCBI]
|
7.54636e-06
|
|
|
AHR
|
[NCBI]
|
7.39046e-06
|
|
|
TYMS
|
[NCBI]
|
6.56504e-06
|
|
|
DHFR
|
[NCBI]
|
5.51401e-06
|
|
|
TNF
|
[NCBI]
|
5.43097e-06
|
|
|
CF
|
[NCBI]
|
2.62106e-06
|
|
|
PTH
|
[NCBI]
|
4.91755e-07
|
|
|
EGF
|
[NCBI]
|
1.06769e-07
|
|