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MeSH keywords -> Related genes, diseases (OMIM)


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01 Cerebral Aqueduct [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 8.69867e-05
L1CAM [NCBI] 2.43455e-05
SSPO [NCBI] 9.18263e-06
DNAH5 [NCBI] 8.71906e-06
VIM [NCBI] 6.00797e-06
VWF [NCBI] 3.78981e-06
VIP [NCBI] 3.28055e-06
GFAP [NCBI] 3.19084e-06
EGF [NCBI] 2.1258e-06




OMIM


OMIM Link Information
gain
01
DWS [NCBI] 0.0025276
HSAS [NCBI] 0.00212903
hydrocephalus due to congenital stenosis of aqueduct of sylvius [NCBI] 0.000460726
enamel hypoplasia, cataracts, and aqueductal stenosis [NCBI] 0.000229418
vacterl association with hydrocephalus, x-linked [NCBI] 0.000152867
hydrocephalus [NCBI] 0.000148131
L1CAM [NCBI] 0.00013826
masa syndrome [NCBI] 0.000117088
NF1 [NCBI] 6.51302e-05
DNAH5 [NCBI] 5.55083e-05
FANCB [NCBI] 5.10336e-05
panencephalitis, subacute sclerosing [NCBI] 3.84455e-05
FTD [NCBI] 3.28549e-05
VIP [NCBI] 7.60886e-06
GFAP [NCBI] 7.07386e-06
EGF [NCBI] 1.45689e-06




Database Center for Life Science