|
OMIM |
Link |
Information gain |
01 |
|
epilepsy, myoclonic, benign adult familial, type 1
|
[NCBI]
|
0.00169869
|
|
|
PPR
|
[NCBI]
|
0.0015281
|
|
|
valproate embryopathy, susceptibility to
|
[NCBI]
|
0.00133439
|
|
|
MAFD2
|
[NCBI]
|
0.00105542
|
|
|
SPS
|
[NCBI]
|
0.000770471
|
|
|
EIG
|
[NCBI]
|
0.000722441
|
|
|
LKS
|
[NCBI]
|
0.000660901
|
|
|
MAFD1
|
[NCBI]
|
0.00065027
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
0.00040625
|
|
|
SMA3
|
[NCBI]
|
0.000300374
|
|
|
SMA4
|
[NCBI]
|
0.000243425
|
|
|
myoclonic epilepsy of unverricht and lundborg
|
[NCBI]
|
0.000154911
|
|
|
SMA1
|
[NCBI]
|
0.000138003
|
|
|
JAE
|
[NCBI]
|
0.00012146
|
|
|
BGS
|
[NCBI]
|
0.000103419
|
|
|
JME
|
[NCBI]
|
9.1008e-05
|
|
|
n-acetylglutamate synthase deficiency
|
[NCBI]
|
8.87415e-05
|
|
|
MTATP8
|
[NCBI]
|
8.81141e-05
|
|
|
myoclonic epilepsy of lafora
|
[NCBI]
|
7.72087e-05
|
|
|
hyperekplexia, hereditary
|
[NCBI]
|
7.47745e-05
|
|
|
SMA2
|
[NCBI]
|
7.47745e-05
|
|
|
succinic semialdehyde dehydrogenase deficiency
|
[NCBI]
|
7.36509e-05
|
|
|
carbamoyl phosphate synthetase i deficiency, hyperammonemia due to
|
[NCBI]
|
7.36509e-05
|
|
|
argininemia
|
[NCBI]
|
6.87575e-05
|
|
|
thyroid carcinoma, papillary
|
[NCBI]
|
6.40389e-05
|
|
|
WHS
|
[NCBI]
|
6.20143e-05
|
|
|
mitochondrial complex iv deficiency
|
[NCBI]
|
6.13794e-05
|
|
|
citrullinemia, classic
|
[NCBI]
|
5.95792e-05
|
|
|
SLE
|
[NCBI]
|
4.75561e-05
|
|
|
SMN2
|
[NCBI]
|
4.53764e-05
|
|
|
SHBG
|
[NCBI]
|
3.71421e-05
|
|
|
BDNF
|
[NCBI]
|
3.64226e-05
|
|
|
PRL
|
[NCBI]
|
3.29661e-05
|
|
|
TAGLN2
|
[NCBI]
|
3.19791e-05
|
|
|
CF
|
[NCBI]
|
3.07111e-05
|
|
|
SLC18A1
|
[NCBI]
|
2.66247e-05
|
|
|
SLC6A3
|
[NCBI]
|
2.61657e-05
|
|
|
PRKCA
|
[NCBI]
|
2.40103e-05
|
|
|
SLC5A5
|
[NCBI]
|
2.20242e-05
|
|
|
TH
|
[NCBI]
|
2.03726e-05
|
|
|
PRODH
|
[NCBI]
|
2.0235e-05
|
|
|
CFLAR
|
[NCBI]
|
1.99082e-05
|
|
|
FASN
|
[NCBI]
|
1.97522e-05
|
|
|
AVP
|
[NCBI]
|
1.95604e-05
|
|
|
DNAJC5
|
[NCBI]
|
1.94532e-05
|
|
|
GRIA1
|
[NCBI]
|
1.82858e-05
|
|
|
FLNA
|
[NCBI]
|
1.75295e-05
|
|
|
OTC
|
[NCBI]
|
1.68693e-05
|
|
|
ENPEP
|
[NCBI]
|
1.62052e-05
|
|
|
protein c deficiency, congenital thrombotic disease due to
|
[NCBI]
|
1.57578e-05
|
|
|
MTTL1
|
[NCBI]
|
1.54797e-05
|
|
|
SMN1
|
[NCBI]
|
1.47847e-05
|
|
|
STAT6
|
[NCBI]
|
1.4726e-05
|
|
|
GPT
|
[NCBI]
|
1.4726e-05
|
|
|
HDAC1
|
[NCBI]
|
1.34427e-05
|
|
|
MAPK1
|
[NCBI]
|
1.34427e-05
|
|
|
PRKCM
|
[NCBI]
|
1.30925e-05
|
|
|
GDNF
|
[NCBI]
|
1.19135e-05
|
|
|
DNMT1
|
[NCBI]
|
1.09607e-05
|
|
|
IHH
|
[NCBI]
|
1.08254e-05
|
|
|
SLC18A3
|
[NCBI]
|
1.05405e-05
|
|
|
TG
|
[NCBI]
|
9.23512e-06
|
|
|
NR1I2
|
[NCBI]
|
8.36547e-06
|
|
|
CRH
|
[NCBI]
|
7.20375e-06
|
|
|
TPO
|
[NCBI]
|
6.46538e-06
|
|
|
ABCC1
|
[NCBI]
|
6.43506e-06
|
|
|
VEGF
|
[NCBI]
|
4.3561e-06
|
|
|
MDD
|
[NCBI]
|
4.08215e-06
|
|
|
GAPDH
|
[NCBI]
|
3.50787e-06
|
|
|
SHH
|
[NCBI]
|
3.30411e-06
|
|
|
APOB
|
[NCBI]
|
3.02073e-06
|
|
|
PPARA
|
[NCBI]
|
2.99049e-06
|
|
|
PTH
|
[NCBI]
|
2.69073e-06
|
|
|
KLK3
|
[NCBI]
|
1.52746e-06
|
|
|
NGFB
|
[NCBI]
|
9.59998e-07
|
|
|
CAT
|
[NCBI]
|
5.73037e-07
|
|
|
NPY
|
[NCBI]
|
2.83302e-07
|
|
|
AR
|
[NCBI]
|
2.15067e-07
|
|
|
AFP
|
[NCBI]
|
1.94981e-07
|
|