|
OMIM |
Link |
Information gain |
01 |
|
G6PD
|
[NCBI]
|
0.0017555
|
|
|
cholestasis-lymphedema syndrome
|
[NCBI]
|
0.000948879
|
|
|
fatty metamorphosis of viscera
|
[NCBI]
|
0.000900049
|
|
|
hyperbilirubinemia, transient familial neonatal
|
[NCBI]
|
0.000448749
|
|
|
ALGS1
|
[NCBI]
|
0.000202342
|
|
|
hemochromatosis, neonatal
|
[NCBI]
|
0.00017481
|
|
|
UGT1A1
|
[NCBI]
|
0.000167318
|
|
|
TTP
|
[NCBI]
|
0.000153633
|
|
|
edinburgh malformation syndrome
|
[NCBI]
|
0.000111098
|
|
|
EHBA
|
[NCBI]
|
8.70536e-05
|
|
|
citrullinemia, type ii, neonatal-onset
|
[NCBI]
|
8.27066e-05
|
|
|
elliptocytosis, rhesus-unlinked type
|
[NCBI]
|
8.27066e-05
|
|
|
glutathione synthetase deficiency
|
[NCBI]
|
8.09059e-05
|
|
|
crigler-najjar syndrome, type ii
|
[NCBI]
|
7.78148e-05
|
|
|
anemia, dyserythropoietic congenital, type i
|
[NCBI]
|
7.10309e-05
|
|
|
EL1
|
[NCBI]
|
6.771e-05
|
|
|
crigler-najjar syndrome
|
[NCBI]
|
6.56048e-05
|
|
|
NR1I3
|
[NCBI]
|
6.17915e-05
|
|
|
DJS
|
[NCBI]
|
5.4968e-05
|
|
|
galactosemia
|
[NCBI]
|
5.33665e-05
|
|
|
AHCY
|
[NCBI]
|
5.07153e-05
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
4.84389e-05
|
|
|
SLC25A13
|
[NCBI]
|
4.32962e-05
|
|
|
ACP1
|
[NCBI]
|
4.23054e-05
|
|
|
wilson disease
|
[NCBI]
|
4.15456e-05
|
|
|
ZS
|
[NCBI]
|
4.0314e-05
|
|
|
GPX1
|
[NCBI]
|
3.84564e-05
|
|
|
ADAMTS13
|
[NCBI]
|
3.57011e-05
|
|
|
CEL
|
[NCBI]
|
3.52325e-05
|
|
|
AFP
|
[NCBI]
|
3.50682e-05
|
|
|
ADA
|
[NCBI]
|
3.42113e-05
|
|
|
HS
|
[NCBI]
|
2.45229e-05
|
|
|
VEGF
|
[NCBI]
|
1.55856e-05
|
|
|
TNF
|
[NCBI]
|
1.23952e-05
|
|
|
CAT
|
[NCBI]
|
1.06936e-05
|
|
|
TFPI
|
[NCBI]
|
8.03067e-06
|
|
|
HBB
|
[NCBI]
|
4.89089e-06
|
|
|
VIP
|
[NCBI]
|
2.17045e-06
|
|
|
F3
|
[NCBI]
|
1.8254e-06
|
|
|
GFAP
|
[NCBI]
|
4.06942e-08
|
|