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01 Diffuse Cerebral Sclerosis of Schilder [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 0.00073997
PLP1 [NCBI] 0.000402261
POLG [NCBI] 0.000228941
MYT1 [NCBI] 6.01415e-05
CRYAB [NCBI] 1.69798e-05
ABAT [NCBI] 1.24076e-05
LMNB1 [NCBI] 1.03605e-05
MAG [NCBI] 8.11949e-06
ASPA [NCBI] 8.00275e-06
TYROBP [NCBI] 7.96555e-06
NOS2 [NCBI] 6.40294e-06
MBP [NCBI] 6.35255e-06
ABCD1 [NCBI] 5.99647e-06
IAPP [NCBI] 5.44286e-06
PMP22 [NCBI] 4.24118e-06
PTGS1 [NCBI] 3.2731e-06
CASP9 [NCBI] 2.86744e-06
HIF1A [NCBI] 2.06739e-06
GFAP [NCBI] 1.62976e-06
CFTR [NCBI] 1.15514e-06
CASP3 [NCBI] 1.14714e-06




OMIM


OMIM Link Information
gain
01
ALD [NCBI] 0.0077843
pelizaeus-merzbacher-like disease, autosomal recessive, 2 [NCBI] 0.00537675
PMD [NCBI] 0.00446552
PLP1 [NCBI] 0.00187476
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis [NCBI] 0.00107682
metachromatic leukodystrophy [NCBI] 0.00102996
ASD1 [NCBI] 0.000689681
progeroid syndrome, neonatal [NCBI] 0.000587372
SLE [NCBI] 0.000486939
krabbe disease [NCBI] 0.000442233
adrenoleukodystrophy, autosomal neonatal form [NCBI] 0.000326261
POLG [NCBI] 0.000315544
ABCD1 [NCBI] 0.00028315
canavan disease [NCBI] 0.000268864
SPG2 [NCBI] 0.000211502
leukodystrophy, adult-onset, autosomal dominant [NCBI] 0.000196683
alexander disease [NCBI] 0.000146015
refsum disease, infantile form [NCBI] 0.000130725
MSD [NCBI] 0.000119259
CADASIL [NCBI] 0.000113805
ZS [NCBI] 9.77748e-05
cerebral sclerosis similar to pelizaeus-merzbacher disease [NCBI] 9.4018e-05
megalencephaly with dysmyelination [NCBI] 9.4018e-05
VWM [NCBI] 7.49699e-05
ABAT [NCBI] 6.59934e-05
FEB3 [NCBI] 6.31613e-05
MTTF [NCBI] 5.12523e-05
peroxisomal acyl-coa oxidase deficiency [NCBI] 5.04402e-05
PXMP3 [NCBI] 4.74843e-05
ACOX1 [NCBI] 4.55901e-05
microcephaly with spastic quadriplegia [NCBI] 4.55002e-05
EIF2B5 [NCBI] 4.4764e-05
CRYAB [NCBI] 3.98704e-05
d-bifunctional protein deficiency [NCBI] 3.51481e-05
PSAP [NCBI] 3.41866e-05
INAD1 [NCBI] 3.22459e-05
NBIA1 [NCBI] 2.84165e-05
AHC [NCBI] 2.34032e-05
niemann-pick disease, type a [NCBI] 2.34032e-05
MAG [NCBI] 1.75973e-05
CSA [NCBI] 1.6153e-05
neuraminidase deficiency [NCBI] 1.6153e-05
mucolipidosis ii [NCBI] 1.53995e-05
CMT1A [NCBI] 1.26262e-05
MBP [NCBI] 1.22256e-05
gaucher disease, type i [NCBI] 1.09084e-05
fabry disease [NCBI] 6.19763e-06
TSD [NCBI] 1.9702e-06
GFAP [NCBI] 4.97059e-07
panencephalitis, subacute sclerosing [NCBI] 4.85292e-08




Database Center for Life Science