|
OMIM |
Link |
Information gain |
01 |
|
LIP
|
[NCBI]
|
0.000830168
|
|
|
hyperbilirubinemia, conjugated, type iii
|
[NCBI]
|
0.000140314
|
|
|
thyroid hormonogenesis, genetic defect in, 5
|
[NCBI]
|
9.37927e-05
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
8.47446e-05
|
|
|
PRL
|
[NCBI]
|
8.03003e-05
|
|
|
ehlers-danlos syndrome, type vii, autosomal recessive
|
[NCBI]
|
7.97164e-05
|
|
|
neural tube defects
|
[NCBI]
|
7.10508e-05
|
|
|
gm1-gangliosidosis, type i
|
[NCBI]
|
6.77584e-05
|
|
|
ACHE
|
[NCBI]
|
6.48777e-05
|
|
|
HYAL2
|
[NCBI]
|
5.75277e-05
|
|
|
MEG3
|
[NCBI]
|
5.2444e-05
|
|
|
BMP15
|
[NCBI]
|
5.2444e-05
|
|
|
IL5
|
[NCBI]
|
4.40399e-05
|
|
|
ALB
|
[NCBI]
|
4.21183e-05
|
|
|
TF
|
[NCBI]
|
4.19159e-05
|
|
|
GLB1
|
[NCBI]
|
3.76234e-05
|
|
|
CCL2
|
[NCBI]
|
3.28373e-05
|
|
|
BWS
|
[NCBI]
|
3.17359e-05
|
|
|
polycystic kidneys
|
[NCBI]
|
2.87097e-05
|
|
|
GAL
|
[NCBI]
|
2.57757e-05
|
|
|
PLG
|
[NCBI]
|
2.33663e-05
|
|
|
INS
|
[NCBI]
|
1.99248e-05
|
|
|
FGFR3
|
[NCBI]
|
1.90183e-05
|
|
|
IL2
|
[NCBI]
|
1.67218e-05
|
|
|
SHH
|
[NCBI]
|
1.56569e-05
|
|
|
TLR4
|
[NCBI]
|
1.49384e-05
|
|
|
CJD
|
[NCBI]
|
1.35487e-05
|
|
|
PCNA
|
[NCBI]
|
8.72422e-06
|
|
|
CCK
|
[NCBI]
|
5.63121e-06
|
|
|
CAT
|
[NCBI]
|
5.24694e-06
|
|
|
CRH
|
[NCBI]
|
3.69965e-06
|
|
|
AVP
|
[NCBI]
|
2.56346e-06
|
|
|
VEGF
|
[NCBI]
|
2.533e-06
|
|
|
TNF
|
[NCBI]
|
1.94188e-06
|
|