|
OMIM |
Link |
Information gain |
01 |
|
glycogen storage disease vii
|
[NCBI]
|
0.00610921
|
|
|
PFKM
|
[NCBI]
|
0.00077642
|
|
|
PFKL
|
[NCBI]
|
0.000488565
|
|
|
PFKP
|
[NCBI]
|
0.000307132
|
|
|
GAPDH
|
[NCBI]
|
0.000107336
|
|
|
mitochondrial myopathy
|
[NCBI]
|
0.000101708
|
|
|
GPI
|
[NCBI]
|
0.000100312
|
|
|
RHN
|
[NCBI]
|
9.56145e-05
|
|
|
succinyl-coa:3-oxoacid coa transferase deficiency
|
[NCBI]
|
8.87644e-05
|
|
|
phosphoglycerate kinase 1 deficiency
|
[NCBI]
|
8.51381e-05
|
|
|
AVSD
|
[NCBI]
|
7.80293e-05
|
|
|
uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to
|
[NCBI]
|
7.68442e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, late-onset
|
[NCBI]
|
6.99566e-05
|
|
|
PFKFB4
|
[NCBI]
|
3.62407e-05
|
|
|
PFKFB3
|
[NCBI]
|
3.02707e-05
|
|
|
HK3
|
[NCBI]
|
2.9194e-05
|
|
|
PGAM1
|
[NCBI]
|
2.75328e-05
|
|
|
phosphoglycerate mutase, muscle, deficiency of
|
[NCBI]
|
2.57336e-05
|
|
|
PKM2
|
[NCBI]
|
2.48025e-05
|
|
|
fructose intolerance, hereditary
|
[NCBI]
|
1.81708e-05
|
|
|
RHCE
|
[NCBI]
|
1.74881e-05
|
|
|
EGF
|
[NCBI]
|
1.39767e-05
|
|
|
PC
|
[NCBI]
|
1.27475e-05
|
|
|
PTEN
|
[NCBI]
|
1.1688e-05
|
|
|
G6PD
|
[NCBI]
|
9.10567e-06
|
|
|
AKR1B1
|
[NCBI]
|
7.97708e-06
|
|
|
HD
|
[NCBI]
|
6.09439e-06
|
|
|
GAL
|
[NCBI]
|
5.95819e-06
|
|
|
VEGF
|
[NCBI]
|
5.05776e-06
|
|
|
ADA
|
[NCBI]
|
1.84892e-06
|
|
|
PRL
|
[NCBI]
|
1.55183e-06
|
|
|
PTH
|
[NCBI]
|
9.38848e-07
|
|
|
CHAT
|
[NCBI]
|
4.6722e-07
|
|
|
LPL
|
[NCBI]
|
3.68501e-07
|
|
|
ACHE
|
[NCBI]
|
1.88196e-07
|
|
|
GFAP
|
[NCBI]
|
1.65387e-09
|
|