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MeSH keywords -> Related genes, diseases (OMIM)


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01 Epilepsies, Myoclonic [NCBI]


Gene


Gene Link Information
Gain
01
PPR [NCBI] 0.000389354
BAFME1 [NCBI] 0.000367544
EJM2 [NCBI] 0.000367544
BAFME2 [NCBI] 0.000367544
EJM3 [NCBI] 0.000367544
EIM [NCBI] 0.000367544
SCN1A [NCBI] 0.000357501
CSTB [NCBI] 0.000310422
EGI [NCBI] 0.000306807
EPM2A [NCBI] 0.000132327
ARX [NCBI] 3.49673e-05
EFHC1 [NCBI] 3.05955e-05
GABRG2 [NCBI] 2.9213e-05
SCNN1A [NCBI] 2.88241e-05
SCN1B [NCBI] 2.88241e-05
GABRR2 [NCBI] 2.03833e-05
CDKL5 [NCBI] 1.76292e-05
ATN1 [NCBI] 1.76292e-05
KCNV1 [NCBI] 1.5113e-05
KCNQ2 [NCBI] 1.46128e-05
KCTD7 [NCBI] 1.27328e-05
KCNMB3 [NCBI] 1.27328e-05
CLN3 [NCBI] 1.25814e-05
PCMT1 [NCBI] 1.18345e-05
SLC25A22 [NCBI] 1.18345e-05
PWP2 [NCBI] 1.18345e-05
CSMD2 [NCBI] 1.12513e-05
CSMD3 [NCBI] 1.12513e-05
EFHC2 [NCBI] 1.12513e-05
TRAPPC10 [NCBI] 1.08177e-05
U2AF1 [NCBI] 1.04721e-05
STXBP1 [NCBI] 1.04721e-05
MRAP [NCBI] 1.01849e-05
GABRD [NCBI] 9.93898e-06
CACNB4 [NCBI] 9.72402e-06
NDUFV1 [NCBI] 9.20528e-06
U2AF2 [NCBI] 9.06227e-06
SCO1 [NCBI] 9.06227e-06
CSMD1 [NCBI] 8.93031e-06
SLC12A6 [NCBI] 8.80781e-06
HAX1 [NCBI] 8.13302e-06
SCN8A [NCBI] 8.13302e-06
GABBR1 [NCBI] 7.98078e-06
OPHN1 [NCBI] 7.98078e-06
GABRA1 [NCBI] 7.42626e-06
SGCE [NCBI] 7.13686e-06
CHRNA7 [NCBI] 6.67404e-06
ALDH5A1 [NCBI] 6.57571e-06
SERPINI1 [NCBI] 6.57571e-06
CTSB [NCBI] 6.23129e-06
NDP [NCBI] 6.10626e-06
DDB2 [NCBI] 5.96755e-06
UBE3A [NCBI] 5.36021e-06
GBA [NCBI] 5.18473e-06
ATP7A [NCBI] 4.72722e-06
TOR1A [NCBI] 4.37006e-06
GRM5 [NCBI] 4.32842e-06
PSEN1 [NCBI] 3.91721e-06
PAX6 [NCBI] 3.68135e-06
GFAP [NCBI] 3.32742e-06
PMP22 [NCBI] 3.13751e-06
MECP2 [NCBI] 3.10329e-06
CST3 [NCBI] 2.111e-06
TRH [NCBI] 1.75636e-06
BDNF [NCBI] 1.53187e-06
NGF [NCBI] 6.9366e-07
PRL [NCBI] 5.46926e-07




OMIM


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




Database Center for Life Science