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MeSH keywords -> Related genes, diseases (OMIM)


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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