Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Brain Damage, Chronic [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.000697752
ANE1 [NCBI] 0.000264926
MBP [NCBI] 4.03224e-05
GFAP [NCBI] 3.66902e-05
TREX1 [NCBI] 2.26336e-05
S100B [NCBI] 1.83049e-05
MAP2 [NCBI] 1.45438e-05
PPP3CB [NCBI] 1.20482e-05
GALR2 [NCBI] 1.20482e-05
SUOX [NCBI] 1.15147e-05
IL1B [NCBI] 9.61565e-06
DDC [NCBI] 8.49864e-06
BDNF [NCBI] 8.13616e-06
NEFM [NCBI] 7.51039e-06
INHBA [NCBI] 7.42438e-06
GER [NCBI] 7.27658e-06
MAPK14 [NCBI] 6.08805e-06
NEFL [NCBI] 6.03189e-06
PSEN1 [NCBI] 5.45382e-06
NEFH [NCBI] 5.38991e-06
APOE [NCBI] 5.3645e-06
PARP1 [NCBI] 5.21174e-06
ALDH2 [NCBI] 5.13472e-06
SLC2A1 [NCBI] 4.54856e-06
HMOX1 [NCBI] 4.51506e-06
PON1 [NCBI] 4.38417e-06
COMT [NCBI] 4.1242e-06
CCL2 [NCBI] 3.70022e-06
APC [NCBI] 3.2565e-06
TRH [NCBI] 3.17403e-06
CCK [NCBI] 3.08986e-06
TLR4 [NCBI] 3.06039e-06
CAT [NCBI] 2.91716e-06
TH [NCBI] 2.85359e-06
ACHE [NCBI] 2.81351e-06
MTHFR [NCBI] 2.7745e-06
CD68 [NCBI] 2.66896e-06
IL1RN [NCBI] 2.50232e-06
NOS2 [NCBI] 2.47766e-06
EPO [NCBI] 1.91499e-06
NGF [NCBI] 1.91178e-06
CASP3 [NCBI] 1.47799e-06
PTGS2 [NCBI] 1.14451e-06



OMIM


 OMIM Link Information
gain		 01
necrotizing encephalopathy, acute, autosomal dominant [NCBI] 0.00107364
autism [NCBI] 0.000553779
AGS1 [NCBI] 0.000155665
MBP [NCBI] 0.000155125
GFAP [NCBI] 0.000133927
senile plaque formation [NCBI] 0.000131018
reese retinal dysplasia [NCBI] 0.000131018
craniofacial dyssynostosis with short stature [NCBI] 0.000100073
pyridoxamine 5-prime-phosphate oxidase deficiency [NCBI] 0.000100073
panencephalitis, subacute sclerosing [NCBI] 8.96266e-05
ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant [NCBI] 8.72191e-05
cerebral palsy, spastic, symmetric, autosomal recessive [NCBI] 8.0164e-05
apnea, obstructive sleep [NCBI] 7.89651e-05
glutathione synthetase deficiency [NCBI] 7.8364e-05
MAP2 [NCBI] 6.74993e-05
GALR2 [NCBI] 6.55281e-05
PNPO [NCBI] 6.55281e-05
crigler-najjar syndrome [NCBI] 6.30739e-05
alzheimer disease 3 [NCBI] 6.06417e-05
autonomic control, congenital failure of [NCBI] 5.90339e-05
MTHFD1 [NCBI] 5.45574e-05
ADHD [NCBI] 5.17951e-05
HHF2 [NCBI] 4.88614e-05
PTGS2 [NCBI] 3.32733e-05
dystrophia myotonica 1 [NCBI] 2.7491e-05
RTT [NCBI] 2.64999e-05
ADCYAP1 [NCBI] 2.62519e-05
BDNF [NCBI] 2.55071e-05
GTS [NCBI] 1.93524e-05
TLR4 [NCBI] 1.68847e-05
COMT [NCBI] 1.6479e-05
APOE [NCBI] 1.63969e-05
GDNF [NCBI] 1.34922e-05
AD [NCBI] 1.20038e-05
NPPA [NCBI] 8.98163e-06
G6PD [NCBI] 7.89409e-06
CCK [NCBI] 7.22422e-06
CAT [NCBI] 6.81096e-06
CJD [NCBI] 6.6813e-06
SLE [NCBI] 6.47722e-06
ACHE [NCBI] 5.95947e-06
EPO [NCBI] 2.31752e-06
NGFB [NCBI] 2.22843e-06



Database Center for Life Science