|
OMIM |
Link |
Information gain |
01 |
|
MENOQ1
|
[NCBI]
|
0.00296772
|
|
|
cataract and cardiomyopathy
|
[NCBI]
|
0.00202368
|
|
|
galactosemia
|
[NCBI]
|
0.00160513
|
|
|
GGM
|
[NCBI]
|
0.00125418
|
|
|
galactokinase deficiency
|
[NCBI]
|
0.000912154
|
|
|
AKR1B1
|
[NCBI]
|
0.000495918
|
|
|
galactose epimerase deficiency
|
[NCBI]
|
0.000479799
|
|
|
FBS
|
[NCBI]
|
0.000256373
|
|
|
mullerian aplasia
|
[NCBI]
|
0.000250063
|
|
|
GALK1
|
[NCBI]
|
0.000246182
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
0.000200921
|
|
|
SLE
|
[NCBI]
|
0.000151536
|
|
|
SLC5A1
|
[NCBI]
|
0.00015072
|
|
|
CDG2D
|
[NCBI]
|
0.000146658
|
|
|
krabbe disease
|
[NCBI]
|
0.000144766
|
|
|
glycogen storage disease iii
|
[NCBI]
|
0.000131976
|
|
|
gm1-gangliosidosis, type i
|
[NCBI]
|
0.000130292
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
0.000113959
|
|
|
lactase persistence
|
[NCBI]
|
0.000111751
|
|
|
GALE
|
[NCBI]
|
0.000110363
|
|
|
lactase deficiency, congenital
|
[NCBI]
|
8.97875e-05
|
|
|
B4GALT1
|
[NCBI]
|
8.34024e-05
|
|
|
GLYS1
|
[NCBI]
|
8.14559e-05
|
|
|
glycogen storage disease 0, liver
|
[NCBI]
|
8.14559e-05
|
|
|
SLC2A2
|
[NCBI]
|
8.07517e-05
|
|
|
thyroid hormonogenesis, genetic defect in, 5
|
[NCBI]
|
7.82257e-05
|
|
|
TK1
|
[NCBI]
|
7.26177e-05
|
|
|
morquio syndrome b
|
[NCBI]
|
6.50378e-05
|
|
|
CTLN2
|
[NCBI]
|
6.50378e-05
|
|
|
MBL2
|
[NCBI]
|
6.22312e-05
|
|
|
glycogen storage disease i
|
[NCBI]
|
6.17156e-05
|
|
|
RA
|
[NCBI]
|
5.44037e-05
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
4.63803e-05
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
3.79352e-05
|
|
|
GALT
|
[NCBI]
|
3.47607e-05
|
|
|
GALK2
|
[NCBI]
|
3.2869e-05
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
3.03227e-05
|
|
|
GALM
|
[NCBI]
|
3.00699e-05
|
|
|
RPL39
|
[NCBI]
|
3.00699e-05
|
|
|
G6PD
|
[NCBI]
|
2.93575e-05
|
|
|
ITLN1
|
[NCBI]
|
2.82532e-05
|
|
|
CF
|
[NCBI]
|
2.79618e-05
|
|
|
ST3GAL1
|
[NCBI]
|
2.6903e-05
|
|
|
ST6GAL1
|
[NCBI]
|
2.58277e-05
|
|
|
MEA1
|
[NCBI]
|
2.58277e-05
|
|
|
TRMU
|
[NCBI]
|
2.49339e-05
|
|
|
MAG
|
[NCBI]
|
2.46383e-05
|
|
|
EIF6
|
[NCBI]
|
2.41692e-05
|
|
|
GIP
|
[NCBI]
|
2.29032e-05
|
|
|
MDM1
|
[NCBI]
|
2.23741e-05
|
|
|
fabry disease
|
[NCBI]
|
2.20783e-05
|
|
|
farber lipogranulomatosis
|
[NCBI]
|
2.10362e-05
|
|
|
CHST3
|
[NCBI]
|
2.10362e-05
|
|
|
FUT1
|
[NCBI]
|
2.03018e-05
|
|
|
KSS
|
[NCBI]
|
1.9671e-05
|
|
|
MTTS1
|
[NCBI]
|
1.96575e-05
|
|
|
ERCC6
|
[NCBI]
|
1.96575e-05
|
|
|
LGALS3
|
[NCBI]
|
1.90837e-05
|
|
|
AD
|
[NCBI]
|
1.70806e-05
|
|
|
ERCC5
|
[NCBI]
|
1.68954e-05
|
|
|
MTRNR1
|
[NCBI]
|
1.62259e-05
|
|
|
MTCO1
|
[NCBI]
|
1.54954e-05
|
|
|
fructose intolerance, hereditary
|
[NCBI]
|
1.48559e-05
|
|
|
SLC6A6
|
[NCBI]
|
1.46209e-05
|
|
|
FXN
|
[NCBI]
|
1.38748e-05
|
|
|
CEL
|
[NCBI]
|
1.28878e-05
|
|
|
APOD
|
[NCBI]
|
1.19955e-05
|
|
|
mucopolysaccharidosis type ii
|
[NCBI]
|
1.1125e-05
|
|
|
H6PD
|
[NCBI]
|
1.10684e-05
|
|
|
CAT
|
[NCBI]
|
1.07632e-05
|
|
|
CEACAM5
|
[NCBI]
|
1.07042e-05
|
|
|
FGF1
|
[NCBI]
|
1.05866e-05
|
|
|
PAEP
|
[NCBI]
|
1.03385e-05
|
|
|
TG
|
[NCBI]
|
1.01949e-05
|
|
|
SI
|
[NCBI]
|
9.7481e-06
|
|
|
von willebrand disease
|
[NCBI]
|
9.00026e-06
|
|
|
OMP
|
[NCBI]
|
8.78721e-06
|
|
|
HMBS
|
[NCBI]
|
8.08186e-06
|
|
|
CNTF
|
[NCBI]
|
7.72125e-06
|
|
|
MG
|
[NCBI]
|
5.88904e-06
|
|
|
EGF
|
[NCBI]
|
5.34241e-06
|
|
|
SDC2
|
[NCBI]
|
5.23281e-06
|
|
|
PI
|
[NCBI]
|
4.98814e-06
|
|
|
STAR
|
[NCBI]
|
4.50642e-06
|
|
|
GPI
|
[NCBI]
|
4.48215e-06
|
|
|
VEGF
|
[NCBI]
|
4.18146e-06
|
|
|
ACHE
|
[NCBI]
|
2.3934e-06
|
|
|
NGFB
|
[NCBI]
|
1.92044e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
1.48984e-06
|
|
|
GFAP
|
[NCBI]
|
1.44553e-06
|
|
|
TTR
|
[NCBI]
|
1.36019e-06
|
|
|
VIP
|
[NCBI]
|
1.33017e-06
|
|
|
CHAT
|
[NCBI]
|
1.2081e-06
|
|
|
PCNA
|
[NCBI]
|
1.0844e-06
|
|
|
BDNF
|
[NCBI]
|
8.92382e-07
|
|
|
MBP
|
[NCBI]
|
6.58253e-07
|
|
|
HGF
|
[NCBI]
|
5.76361e-07
|
|
|
AFP
|
[NCBI]
|
3.90079e-07
|
|
|
PTK2
|
[NCBI]
|
3.26689e-07
|
|
|
PRL
|
[NCBI]
|
2.22494e-07
|
|
|
CFTR
|
[NCBI]
|
1.55603e-08
|
|
|
EPO
|
[NCBI]
|
8.56086e-09
|
|