|
OMIM |
Link |
Information gain |
01 |
|
CDAN2
|
[NCBI]
|
0.0020554
|
|
|
UGCG
|
[NCBI]
|
0.00140265
|
|
|
CDG1C
|
[NCBI]
|
0.00106941
|
|
|
glycogen storage disease iv
|
[NCBI]
|
0.00054224
|
|
|
glycogen storage disease iii
|
[NCBI]
|
0.000516205
|
|
|
glycogen storage disease v
|
[NCBI]
|
0.000370397
|
|
|
CDG1H
|
[NCBI]
|
0.000322932
|
|
|
ALG6
|
[NCBI]
|
0.00025444
|
|
|
LNS
|
[NCBI]
|
0.000220689
|
|
|
crigler-najjar syndrome
|
[NCBI]
|
0.000177557
|
|
|
GYG
|
[NCBI]
|
0.000169408
|
|
|
hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase
|
[NCBI]
|
0.000161251
|
|
|
CDG1A
|
[NCBI]
|
0.000138316
|
|
|
MGAT1
|
[NCBI]
|
0.00013338
|
|
|
epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase
|
[NCBI]
|
0.000129679
|
|
|
syringomas, multiple
|
[NCBI]
|
0.000129679
|
|
|
myopathy with storage of glycoproteins and glycosaminoglycans
|
[NCBI]
|
0.000117775
|
|
|
CDG1K
|
[NCBI]
|
0.000117775
|
|
|
corneal dystrophy, juvenile epithelial, of meesmann
|
[NCBI]
|
0.00011005
|
|
|
hyperbilirubinemia, transient familial neonatal
|
[NCBI]
|
9.97421e-05
|
|
|
HPRT1
|
[NCBI]
|
9.9279e-05
|
|
|
RFNG
|
[NCBI]
|
9.63096e-05
|
|
|
LGMD2H
|
[NCBI]
|
9.59454e-05
|
|
|
glycogen storage disease 0, liver
|
[NCBI]
|
9.59454e-05
|
|
|
gout, hprt-related
|
[NCBI]
|
9.26979e-05
|
|
|
mucolipidosis iii, complementation group c
|
[NCBI]
|
8.9861e-05
|
|
|
CDG1B
|
[NCBI]
|
8.73428e-05
|
|
|
brody myopathy
|
[NCBI]
|
8.50793e-05
|
|
|
GYG2
|
[NCBI]
|
8.45957e-05
|
|
|
ehlers-danlos syndrome, type vii, autosomal dominant
|
[NCBI]
|
8.30238e-05
|
|
|
crigler-najjar syndrome, type ii
|
[NCBI]
|
8.30238e-05
|
|
|
helicobacter pylori infection, susceptibility to
|
[NCBI]
|
7.94061e-05
|
|
|
mucolipidosis iiia
|
[NCBI]
|
7.48888e-05
|
|
|
gilbert syndrome
|
[NCBI]
|
7.11382e-05
|
|
|
glycogen storage disease ixa
|
[NCBI]
|
7.08411e-05
|
|
|
alg8, s. cerevisiae, homolog of
|
[NCBI]
|
6.97526e-05
|
|
|
ALG10
|
[NCBI]
|
6.97526e-05
|
|
|
phosphoribosylpyrophosphate synthetase superactivity
|
[NCBI]
|
6.89509e-05
|
|
|
glycogen storage disease i
|
[NCBI]
|
6.76715e-05
|
|
|
glycogen storage disease ib
|
[NCBI]
|
6.51385e-05
|
|
|
OGT
|
[NCBI]
|
6.05173e-05
|
|
|
MFNG
|
[NCBI]
|
5.66845e-05
|
|
|
glycogen storage disease vii
|
[NCBI]
|
5.65783e-05
|
|
|
MHS1
|
[NCBI]
|
4.8383e-05
|
|
|
LFNG
|
[NCBI]
|
4.53032e-05
|
|
|
ALG5
|
[NCBI]
|
4.22711e-05
|
|
|
ABO
|
[NCBI]
|
4.2149e-05
|
|
|
TRIM7
|
[NCBI]
|
3.48495e-05
|
|
|
UGT8
|
[NCBI]
|
3.20496e-05
|
|
|
ALG1
|
[NCBI]
|
3.0232e-05
|
|
|
slu7, s. cerevisiae, homolog of
|
[NCBI]
|
3.0232e-05
|
|
|
POFUT2
|
[NCBI]
|
2.88809e-05
|
|
|
LYPLA3
|
[NCBI]
|
2.78046e-05
|
|
|
PLOD3
|
[NCBI]
|
2.78046e-05
|
|
|
TRIM32
|
[NCBI]
|
2.691e-05
|
|
|
EEF1A1
|
[NCBI]
|
2.61443e-05
|
|
|
POFUT1
|
[NCBI]
|
2.61443e-05
|
|
|
POMGNT1
|
[NCBI]
|
2.4881e-05
|
|
|
ATP2A1
|
[NCBI]
|
2.38611e-05
|
|
|
FUT3
|
[NCBI]
|
2.34163e-05
|
|
|
EN1
|
[NCBI]
|
2.3006e-05
|
|
|
TK1
|
[NCBI]
|
2.00567e-05
|
|
|
PMM2
|
[NCBI]
|
1.98355e-05
|
|
|
orotic aciduria i
|
[NCBI]
|
1.98355e-05
|
|
|
fructose intolerance, hereditary
|
[NCBI]
|
1.67988e-05
|
|
|
TLR5
|
[NCBI]
|
1.61188e-05
|
|
|
UGT1A1
|
[NCBI]
|
1.43413e-05
|
|
|
CF
|
[NCBI]
|
9.0425e-06
|
|
|
EGF
|
[NCBI]
|
3.99706e-06
|
|
|
G6PD
|
[NCBI]
|
1.05309e-06
|
|
|
DHFR
|
[NCBI]
|
8.36288e-07
|
|
|
NGFB
|
[NCBI]
|
1.69786e-07
|
|
|
LPL
|
[NCBI]
|
4.70033e-08
|
|
|
TNF
|
[NCBI]
|
1.89143e-08
|
|