MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Hereditary Central Nervous System Demyelinating Diseases
[NCBI]
Gene
Gene
Link
Information
Gain
01
NEWENTRY
[NCBI]
0.000157063
MLC1
[NCBI]
0.000123867
EIF2B4
[NCBI]
7.03336e-05
EIF2B5
[NCBI]
5.24911e-05
FAM126A
[NCBI]
4.36782e-05
EIF2B1
[NCBI]
4.08192e-05
EIF2B2
[NCBI]
4.02997e-05
MS
[NCBI]
3.75925e-05
PLP1
[NCBI]
2.91917e-05
EIF2B3
[NCBI]
2.63566e-05
GJB1
[NCBI]
1.2949e-05
GPM6B
[NCBI]
1.26056e-05
PRX
[NCBI]
1.13376e-05
LMNB1
[NCBI]
1.13376e-05
TREM2
[NCBI]
1.02635e-05
ERN1
[NCBI]
9.84126e-06
ATF6
[NCBI]
9.22028e-06
ATF4
[NCBI]
9.05493e-06
EGR2
[NCBI]
9.05493e-06
TYROBP
[NCBI]
8.94063e-06
HSPD1
[NCBI]
8.20364e-06
TREM1
[NCBI]
7.45899e-06
MPZ
[NCBI]
7.39822e-06
TNFRSF1A
[NCBI]
6.98906e-06
PMP22
[NCBI]
5.19496e-06
MBP
[NCBI]
2.96471e-06
GFAP
[NCBI]
2.48185e-06
OMIM
OMIM
Link
Information
gain
01
leukodystrophy, adult-onset, autosomal dominant
[NCBI]
0.000478183
hypomyelination and congenital cataract
[NCBI]
0.000281709
VWM
[NCBI]
0.000273586
EIF2B5
[NCBI]
0.000207089
MLC
[NCBI]
0.000167471
PMD
[NCBI]
0.000113789
pelizaeus-merzbacher-like disease, autosomal recessive, 1
[NCBI]
0.000103859
neuropathy, congenital hypomyelinating
[NCBI]
7.87053e-05
EIF2B3
[NCBI]
7.77884e-05
FAM126A
[NCBI]
7.77884e-05
LMNB1
[NCBI]
7.25879e-05
EIF2B2
[NCBI]
6.9211e-05
EIF2B4
[NCBI]
6.67002e-05
GJC2
[NCBI]
6.46996e-05
hypertrophic neuropathy of dejerine-sottas
[NCBI]
6.13123e-05
MLC1
[NCBI]
6.03671e-05
SURF1
[NCBI]
5.57696e-05
PRX
[NCBI]
5.57696e-05
GDAP1
[NCBI]
5.50599e-05
LS
[NCBI]
5.09661e-05
PLP1
[NCBI]
4.21176e-05
MPZ
[NCBI]
3.71477e-05
MAG
[NCBI]
2.8933e-05
SHH
[NCBI]
2.43406e-05
MBP
[NCBI]
9.9327e-06
GFAP
[NCBI]
7.34895e-06
Database Center for Life Science