|
OMIM |
Link |
Information gain |
01 |
|
CTS1
|
[NCBI]
|
0.00995263
|
|
|
carnitine deficiency, myopathic
|
[NCBI]
|
0.00241196
|
|
|
arthrogryposis-like disorder
|
[NCBI]
|
0.00213118
|
|
|
UFS
|
[NCBI]
|
0.00141296
|
|
|
ATD1
|
[NCBI]
|
0.00141296
|
|
|
hydroxykynureninuria
|
[NCBI]
|
0.00119189
|
|
|
WDM
|
[NCBI]
|
0.00105525
|
|
|
stomatocytosis i
|
[NCBI]
|
0.000716204
|
|
|
GPT
|
[NCBI]
|
0.000535499
|
|
|
GOT1
|
[NCBI]
|
0.000380943
|
|
|
CAT
|
[NCBI]
|
0.000380911
|
|
|
PFIC1
|
[NCBI]
|
0.000367984
|
|
|
GOT2
|
[NCBI]
|
0.000287734
|
|
|
cirrhosis, familial
|
[NCBI]
|
0.000266762
|
|
|
ALB
|
[NCBI]
|
0.000196939
|
|
|
MPO
|
[NCBI]
|
0.000177943
|
|
|
cerebellar vermis aplasia with associated features suggesting smith-lemli-opitz syndrome and meckel syndrome
|
[NCBI]
|
0.000154963
|
|
|
cyanosis and hepatic disease
|
[NCBI]
|
0.000154963
|
|
|
convulsive disorder, familial, with prenatal or early onset
|
[NCBI]
|
0.000154963
|
|
|
hepatocellular carcinoma
|
[NCBI]
|
0.000153924
|
|
|
melanoma, uveal
|
[NCBI]
|
0.000152008
|
|
|
glycogen storage disease iii
|
[NCBI]
|
0.000148407
|
|
|
glycine n-methyltransferase deficiency
|
[NCBI]
|
0.000123397
|
|
|
PROA
|
[NCBI]
|
0.000123397
|
|
|
carnitine acetyltransferase deficiency
|
[NCBI]
|
0.000123397
|
|
|
bilirubin, elevated concentrations of, in serum
|
[NCBI]
|
0.000111499
|
|
|
spinal muscular atrophy, proximal, adult, autosomal dominant
|
[NCBI]
|
0.000111499
|
|
|
PDXK
|
[NCBI]
|
0.000104156
|
|
|
HGF
|
[NCBI]
|
0.00010292
|
|
|
AFP
|
[NCBI]
|
9.69676e-05
|
|
|
SLSN1
|
[NCBI]
|
9.34846e-05
|
|
|
kindler syndrome
|
[NCBI]
|
8.9694e-05
|
|
|
mitochondrial myopathy
|
[NCBI]
|
8.9694e-05
|
|
|
CMD3B
|
[NCBI]
|
8.64526e-05
|
|
|
creatine phosphokinase, elevated serum
|
[NCBI]
|
8.64526e-05
|
|
|
LGMD2E
|
[NCBI]
|
8.11098e-05
|
|
|
halothane hepatitis
|
[NCBI]
|
8.11098e-05
|
|
|
EPD
|
[NCBI]
|
7.15938e-05
|
|
|
NPHP1
|
[NCBI]
|
7.00986e-05
|
|
|
FBS
|
[NCBI]
|
6.73826e-05
|
|
|
SMA3
|
[NCBI]
|
6.38518e-05
|
|
|
ACHE
|
[NCBI]
|
6.33602e-05
|
|
|
TNF
|
[NCBI]
|
6.11763e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, late-onset
|
[NCBI]
|
5.81521e-05
|
|
|
ALGS1
|
[NCBI]
|
5.73331e-05
|
|
|
DM2
|
[NCBI]
|
5.65443e-05
|
|
|
LGMD2A
|
[NCBI]
|
5.57835e-05
|
|
|
acyl-coa dehydrogenase, medium-chain, deficiency of
|
[NCBI]
|
5.4339e-05
|
|
|
glycogen storage disease v
|
[NCBI]
|
5.3652e-05
|
|
|
ARPKD
|
[NCBI]
|
5.17155e-05
|
|
|
HP
|
[NCBI]
|
4.8903e-05
|
|
|
DJS
|
[NCBI]
|
4.88387e-05
|
|
|
sandhoff disease
|
[NCBI]
|
4.72859e-05
|
|
|
NPC1
|
[NCBI]
|
3.95064e-05
|
|
|
HK1
|
[NCBI]
|
3.24751e-05
|
|
|
PC
|
[NCBI]
|
3.04901e-05
|
|
|
PTH
|
[NCBI]
|
2.92757e-05
|
|
|
glycogen storage disease ixa
|
[NCBI]
|
2.83674e-05
|
|
|
CSF2
|
[NCBI]
|
2.5882e-05
|
|
|
VEGF
|
[NCBI]
|
2.53107e-05
|
|
|
CKMT1B
|
[NCBI]
|
2.48067e-05
|
|
|
GSTA1
|
[NCBI]
|
2.48067e-05
|
|
|
EGF
|
[NCBI]
|
2.36658e-05
|
|
|
porphyria cutanea tarda
|
[NCBI]
|
2.30309e-05
|
|
|
DMD
|
[NCBI]
|
2.30165e-05
|
|
|
PI12
|
[NCBI]
|
2.29948e-05
|
|
|
CP
|
[NCBI]
|
2.25169e-05
|
|
|
PYCS
|
[NCBI]
|
2.16495e-05
|
|
|
GPX2
|
[NCBI]
|
1.96901e-05
|
|
|
MDH2
|
[NCBI]
|
1.96901e-05
|
|
|
PPA1
|
[NCBI]
|
1.96901e-05
|
|
|
RA
|
[NCBI]
|
1.9622e-05
|
|
|
PGAM1
|
[NCBI]
|
1.89302e-05
|
|
|
TSD
|
[NCBI]
|
1.82179e-05
|
|
|
PEPB
|
[NCBI]
|
1.76783e-05
|
|
|
KLK3
|
[NCBI]
|
1.72922e-05
|
|
|
XDH
|
[NCBI]
|
1.71895e-05
|
|
|
MDH1
|
[NCBI]
|
1.71497e-05
|
|
|
PCNA
|
[NCBI]
|
1.60602e-05
|
|
|
IDH1
|
[NCBI]
|
1.58263e-05
|
|
|
GIST
|
[NCBI]
|
1.54907e-05
|
|
|
PFKL
|
[NCBI]
|
1.54512e-05
|
|
|
NQO1
|
[NCBI]
|
1.54512e-05
|
|
|
MT1A
|
[NCBI]
|
1.54512e-05
|
|
|
ME2
|
[NCBI]
|
1.51017e-05
|
|
|
GPI
|
[NCBI]
|
1.50078e-05
|
|
|
INS
|
[NCBI]
|
1.43553e-05
|
|
|
CRH
|
[NCBI]
|
1.4185e-05
|
|
|
PGM3
|
[NCBI]
|
1.3903e-05
|
|
|
GFAP
|
[NCBI]
|
1.34671e-05
|
|
|
3-@hydroxy-3-methylglutaryl-coa lyase deficiency
|
[NCBI]
|
1.27191e-05
|
|
|
LTC4S
|
[NCBI]
|
1.23143e-05
|
|
|
polycystic kidneys
|
[NCBI]
|
1.22972e-05
|
|
|
CDK4
|
[NCBI]
|
1.2272e-05
|
|
|
EGFR
|
[NCBI]
|
1.21307e-05
|
|
|
LDHA
|
[NCBI]
|
1.15924e-05
|
|
|
GPX1
|
[NCBI]
|
1.09634e-05
|
|
|
PRL
|
[NCBI]
|
1.08475e-05
|
|
|
TPI1
|
[NCBI]
|
1.00283e-05
|
|
|
GNMT
|
[NCBI]
|
9.7917e-06
|
|
|
glycogen storage disease i
|
[NCBI]
|
9.56646e-06
|
|
|
wolman disease
|
[NCBI]
|
9.45777e-06
|
|
|
G6PD
|
[NCBI]
|
9.19739e-06
|
|
|
GSR
|
[NCBI]
|
8.94955e-06
|
|
|
FH
|
[NCBI]
|
8.66957e-06
|
|
|
AR
|
[NCBI]
|
8.61124e-06
|
|
|
OTC
|
[NCBI]
|
8.23822e-06
|
|
|
MMP9
|
[NCBI]
|
7.99802e-06
|
|
|
methemoglobinemia due to deficiency of methemoglobin reductase
|
[NCBI]
|
7.99802e-06
|
|
|
TNFSF6
|
[NCBI]
|
7.93146e-06
|
|
|
TNFSF10
|
[NCBI]
|
7.76277e-06
|
|
|
PI
|
[NCBI]
|
7.49784e-06
|
|
|
UGT1A1
|
[NCBI]
|
7.4837e-06
|
|
|
APOE
|
[NCBI]
|
7.45913e-06
|
|
|
TGFB1
|
[NCBI]
|
7.15038e-06
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
6.18709e-06
|
|
|
AD
|
[NCBI]
|
6.11881e-06
|
|
|
STAT3
|
[NCBI]
|
6.11036e-06
|
|
|
CHAT
|
[NCBI]
|
5.58852e-06
|
|
|
CPB2
|
[NCBI]
|
5.27749e-06
|
|
|
CF
|
[NCBI]
|
5.26254e-06
|
|
|
homocystinuria
|
[NCBI]
|
5.19777e-06
|
|
|
ADA
|
[NCBI]
|
4.65023e-06
|
|
|
LCAT
|
[NCBI]
|
4.53386e-06
|
|
|
PG
|
[NCBI]
|
4.35636e-06
|
|
|
IFNA1
|
[NCBI]
|
4.05783e-06
|
|
|
ABCB1
|
[NCBI]
|
4.02939e-06
|
|
|
HFE
|
[NCBI]
|
3.04127e-06
|
|
|
SLE
|
[NCBI]
|
3.02298e-06
|
|
|
CYP1A1
|
[NCBI]
|
2.92938e-06
|
|
|
EPO
|
[NCBI]
|
2.82942e-06
|
|
|
CEACAM5
|
[NCBI]
|
2.74681e-06
|
|
|
MBP
|
[NCBI]
|
2.51281e-06
|
|
|
CD
|
[NCBI]
|
2.27379e-06
|
|
|
ABP1
|
[NCBI]
|
2.20393e-06
|
|
|
VDR
|
[NCBI]
|
1.86824e-06
|
|
|
TLR2
|
[NCBI]
|
1.79929e-06
|
|
|
LPL
|
[NCBI]
|
1.7729e-06
|
|
|
TG
|
[NCBI]
|
1.72027e-06
|
|
|
SOD1
|
[NCBI]
|
1.56809e-06
|
|
|
TTR
|
[NCBI]
|
1.2194e-06
|
|
|
DHFR
|
[NCBI]
|
9.40133e-07
|
|
|
BCHE
|
[NCBI]
|
9.07818e-07
|
|
|
GJA1
|
[NCBI]
|
8.86927e-07
|
|
|
AHR
|
[NCBI]
|
6.07554e-07
|
|
|
ACPP
|
[NCBI]
|
5.82648e-07
|
|
|
SHBG
|
[NCBI]
|
5.63669e-07
|
|
|
SPP1
|
[NCBI]
|
4.77539e-07
|
|
|
APOB
|
[NCBI]
|
4.41142e-07
|
|
|
PPARA
|
[NCBI]
|
4.19611e-07
|
|
|
F3
|
[NCBI]
|
4.07738e-07
|
|
|
TYMS
|
[NCBI]
|
1.69222e-07
|
|
|
MB
|
[NCBI]
|
1.50424e-07
|
|
|
IL2
|
[NCBI]
|
2.68858e-08
|
|
|
ACP5
|
[NCBI]
|
2.21342e-08
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
6.31735e-09
|
|