MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Cerebellar Nuclei
[NCBI]
Gene
Gene
Link
Information
Gain
01
SCA20
[NCBI]
0.000510938
MS
[NCBI]
2.57971e-05
CDKL2
[NCBI]
1.71514e-05
ATN1
[NCBI]
1.45176e-05
ALDH5A1
[NCBI]
1.37576e-05
CDH4
[NCBI]
1.26829e-05
RELN
[NCBI]
8.66201e-06
INA
[NCBI]
7.79269e-06
AP1S2
[NCBI]
7.00278e-06
CALB2
[NCBI]
6.69226e-06
CHAT
[NCBI]
5.69197e-06
KLC1
[NCBI]
5.59302e-06
ATXN2
[NCBI]
5.50786e-06
PANK2
[NCBI]
5.45488e-06
ASCL1
[NCBI]
5.34505e-06
CCK
[NCBI]
5.06388e-06
HAPLN1
[NCBI]
4.36654e-06
NGFR
[NCBI]
4.25616e-06
NTN1
[NCBI]
4.05077e-06
HFE
[NCBI]
3.94363e-06
TFRC
[NCBI]
3.74274e-06
MAPT
[NCBI]
3.57017e-06
PAX6
[NCBI]
3.06366e-06
CD68
[NCBI]
2.55668e-06
AVP
[NCBI]
1.97631e-06
GFAP
[NCBI]
1.73003e-06
TH
[NCBI]
1.61298e-06
NPY
[NCBI]
1.51369e-06
OMIM
OMIM
Link
Information
gain
01
IBGC1
[NCBI]
0.00318854
basal ganglia calcification, idiopathic, childhood-onset
[NCBI]
0.00227639
DRPLA
[NCBI]
0.00192697
nystagmus, voluntary
[NCBI]
0.00154746
opticocochleodentate degeneration
[NCBI]
0.00123667
SCA20
[NCBI]
0.00123667
IOSCA
[NCBI]
0.000942047
MJD
[NCBI]
0.00046523
amyotrophic lateral sclerosis with polyglucosan bodies
[NCBI]
0.00021531
haw river syndrome
[NCBI]
0.000161236
myoclonus and ataxia
[NCBI]
0.000151622
MRX59
[NCBI]
0.000144477
myoclonic epilepsy of unverricht and lundborg
[NCBI]
9.78539e-05
CRH
[NCBI]
9.75596e-05
DRPLA
[NCBI]
8.89991e-05
fabry disease
[NCBI]
6.41014e-05
SMAX1
[NCBI]
5.59427e-05
AP1S2
[NCBI]
4.8888e-05
CACNA1A
[NCBI]
3.42238e-05
TS
[NCBI]
3.13604e-05
ALD
[NCBI]
2.86495e-05
NGFR
[NCBI]
2.32337e-05
CHAT
[NCBI]
2.05101e-05
CCK
[NCBI]
1.63965e-05
AVP
[NCBI]
1.57825e-05
GFAP
[NCBI]
3.37726e-06
TH
[NCBI]
2.74676e-06
NPY
[NCBI]
2.25644e-06
AD
[NCBI]
1.2903e-06
Database Center for Life Science