|
OMIM |
Link |
Information gain |
01 |
|
phenylketonuria
|
[NCBI]
|
0.0140807
|
|
|
methionine malabsorption syndrome
|
[NCBI]
|
0.00222949
|
|
|
phenylketonuria ii
|
[NCBI]
|
0.00121156
|
|
|
folic acid, transport defect involving
|
[NCBI]
|
0.000798231
|
|
|
PTS
|
[NCBI]
|
0.000677033
|
|
|
gtp cyclohydrolase i deficiency
|
[NCBI]
|
0.000470678
|
|
|
SPR
|
[NCBI]
|
0.000170681
|
|
|
maple syrup urine disease
|
[NCBI]
|
0.000127806
|
|
|
SC
|
[NCBI]
|
0.000113311
|
|
|
methylmalonyl-coa epimerase deficiency
|
[NCBI]
|
0.000104833
|
|
|
hyperphenylalaninemia with primapterinuria
|
[NCBI]
|
0.000104833
|
|
|
PCBD1
|
[NCBI]
|
9.16715e-05
|
|
|
MRT1
|
[NCBI]
|
8.69446e-05
|
|
|
hyperbilirubinemia, transient familial neonatal
|
[NCBI]
|
8.69446e-05
|
|
|
elliptocytosis, rhesus-unlinked type
|
[NCBI]
|
8.49166e-05
|
|
|
cystathioninuria
|
[NCBI]
|
7.86743e-05
|
|
|
GAL3ST1
|
[NCBI]
|
7.15044e-05
|
|
|
histidinemia
|
[NCBI]
|
6.65411e-05
|
|
|
RP1
|
[NCBI]
|
6.42765e-05
|
|
|
GCH1
|
[NCBI]
|
5.39232e-05
|
|
|
SDS
|
[NCBI]
|
4.68636e-05
|
|
|
CF
|
[NCBI]
|
4.62629e-05
|
|
|
HGD
|
[NCBI]
|
2.6944e-05
|
|
|
ALD
|
[NCBI]
|
2.29949e-05
|
|
|
aspartylglucosaminuria
|
[NCBI]
|
1.91537e-05
|
|
|
ADIPOQ
|
[NCBI]
|
1.80024e-05
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
1.75268e-05
|
|
|
GFAP
|
[NCBI]
|
1.65397e-05
|
|
|
SPTA1
|
[NCBI]
|
1.33485e-05
|
|
|
HNF1A
|
[NCBI]
|
1.30455e-05
|
|
|
PRL
|
[NCBI]
|
1.20217e-05
|
|
|
ACADM
|
[NCBI]
|
9.63382e-06
|
|
|
MYOC
|
[NCBI]
|
9.00626e-06
|
|
|
homocystinuria
|
[NCBI]
|
8.05109e-06
|
|
|
TH
|
[NCBI]
|
5.15986e-06
|
|
|
AKR1B1
|
[NCBI]
|
5.13288e-06
|
|
|
MAG
|
[NCBI]
|
3.44926e-06
|
|
|
CAT
|
[NCBI]
|
1.55177e-06
|
|
|
ACHE
|
[NCBI]
|
3.45638e-07
|
|
|
G6PD
|
[NCBI]
|
5.12684e-08
|
|
|
TTR
|
[NCBI]
|
3.10476e-08
|
|
|
APOB
|
[NCBI]
|
1.26371e-08
|
|
|
MBP
|
[NCBI]
|
5.86065e-09
|
|