|
OMIM |
Link |
Information gain |
01 |
|
epilepsy, myoclonic, benign adult familial, type 1
|
[NCBI]
|
0.00731915
|
|
|
myoclonic epilepsy, juvenile, 3
|
[NCBI]
|
0.00475231
|
|
|
myoclonic epilepsy of unverricht and lundborg
|
[NCBI]
|
0.00269199
|
|
|
SMEI
|
[NCBI]
|
0.00268851
|
|
|
EIG
|
[NCBI]
|
0.00176303
|
|
|
ECA1
|
[NCBI]
|
0.00120064
|
|
|
myoclonic epilepsy, neonatal, with suppression-burst pattern
|
[NCBI]
|
0.00112601
|
|
|
MTTK
|
[NCBI]
|
0.000990134
|
|
|
myoclonic epilepsy, infantile
|
[NCBI]
|
0.000925375
|
|
|
myoclonic epilepsy of lafora
|
[NCBI]
|
0.000868999
|
|
|
CSTB
|
[NCBI]
|
0.000863467
|
|
|
DRPLA
|
[NCBI]
|
0.000799786
|
|
|
JME
|
[NCBI]
|
0.000749501
|
|
|
epilepsy, myoclonic, benign adult familial, type 2
|
[NCBI]
|
0.000707844
|
|
|
EJM2
|
[NCBI]
|
0.000626005
|
|
|
PPR
|
[NCBI]
|
0.000588374
|
|
|
MERRF
|
[NCBI]
|
0.000564154
|
|
|
CLN4B
|
[NCBI]
|
0.000476586
|
|
|
SCN1A
|
[NCBI]
|
0.00045638
|
|
|
myoclonus and ataxia
|
[NCBI]
|
0.000342968
|
|
|
DRPLA
|
[NCBI]
|
0.000327379
|
|
|
SLE
|
[NCBI]
|
0.000296173
|
|
|
EPM2A
|
[NCBI]
|
0.000285832
|
|
|
chiari malformation type i
|
[NCBI]
|
0.000269699
|
|
|
FRNS
|
[NCBI]
|
0.000248508
|
|
|
GEFS+
|
[NCBI]
|
0.000246769
|
|
|
JAE
|
[NCBI]
|
0.000140437
|
|
|
EKD1
|
[NCBI]
|
0.000138613
|
|
|
EJM1
|
[NCBI]
|
0.00013449
|
|
|
spastic paraplegia with myoclonic epilepsy
|
[NCBI]
|
0.000101064
|
|
|
EPM3
|
[NCBI]
|
0.000101064
|
|
|
myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders
|
[NCBI]
|
0.000101064
|
|
|
atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus, photomyoclonus, and degenerative neurologic disease
|
[NCBI]
|
0.000101064
|
|
|
INAD1
|
[NCBI]
|
0.000100939
|
|
|
myoclonic epilepsy, progressive
|
[NCBI]
|
7.86229e-05
|
|
|
epilepsy, myoclonic, x-linked, with mental retardation and spasticity
|
[NCBI]
|
7.86229e-05
|
|
|
myoclonic dystonia
|
[NCBI]
|
7.71985e-05
|
|
|
U2AF1
|
[NCBI]
|
7.50334e-05
|
|
|
PWP2H
|
[NCBI]
|
7.50334e-05
|
|
|
MRAP
|
[NCBI]
|
7.50334e-05
|
|
|
TMEM1
|
[NCBI]
|
7.50334e-05
|
|
|
KCTD7
|
[NCBI]
|
7.50334e-05
|
|
|
KCNV1
|
[NCBI]
|
7.50334e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
6.57792e-05
|
|
|
jumping frenchman of maine
|
[NCBI]
|
6.46959e-05
|
|
|
ATCAY
|
[NCBI]
|
6.46959e-05
|
|
|
PCMT1
|
[NCBI]
|
6.12579e-05
|
|
|
CSMD3
|
[NCBI]
|
6.12579e-05
|
|
|
SLC25A22
|
[NCBI]
|
6.12579e-05
|
|
|
mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance
|
[NCBI]
|
6.06316e-05
|
|
|
SLC12A6
|
[NCBI]
|
5.60617e-05
|
|
|
NDUFV1
|
[NCBI]
|
5.60617e-05
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
5.35614e-05
|
|
|
EFHC1
|
[NCBI]
|
5.2689e-05
|
|
|
APBD
|
[NCBI]
|
5.24246e-05
|
|
|
microcephaly with spastic quadriplegia
|
[NCBI]
|
5.24246e-05
|
|
|
CSMD1
|
[NCBI]
|
5.01825e-05
|
|
|
SCN1B
|
[NCBI]
|
4.81861e-05
|
|
|
MTTF
|
[NCBI]
|
4.65268e-05
|
|
|
OPHN1
|
[NCBI]
|
4.38664e-05
|
|
|
GABRG2
|
[NCBI]
|
4.38664e-05
|
|
|
alexander disease
|
[NCBI]
|
3.73057e-05
|
|
|
tay-sachs disease, ab variant
|
[NCBI]
|
3.67303e-05
|
|
|
SGCE
|
[NCBI]
|
3.56647e-05
|
|
|
hyperekplexia, hereditary
|
[NCBI]
|
3.50807e-05
|
|
|
MELAS
|
[NCBI]
|
3.25547e-05
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
3.19859e-05
|
|
|
ARX
|
[NCBI]
|
3.19386e-05
|
|
|
aspartylglucosaminuria
|
[NCBI]
|
3.12748e-05
|
|
|
gaucher disease, type iii
|
[NCBI]
|
3.04025e-05
|
|
|
mitochondrial complex iv deficiency
|
[NCBI]
|
2.81001e-05
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
2.8039e-05
|
|
|
GBA
|
[NCBI]
|
2.13141e-05
|
|
|
ND
|
[NCBI]
|
1.86987e-05
|
|
|
gaucher disease, type i
|
[NCBI]
|
1.66005e-05
|
|
|
LS
|
[NCBI]
|
1.43848e-05
|
|
|
GFAP
|
[NCBI]
|
1.04002e-05
|
|
|
KSS
|
[NCBI]
|
8.18625e-06
|
|
|
CRH
|
[NCBI]
|
6.89968e-06
|
|
|
BDNF
|
[NCBI]
|
1.07734e-06
|
|
|
PRL
|
[NCBI]
|
7.52144e-07
|
|
|
NGFB
|
[NCBI]
|
2.12103e-07
|
|