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MeSH keywords -> Related genes, diseases (OMIM)


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01 Meningomyelocele [NCBI]

Gene


 Gene Link Information
Gain		 01
VUR [NCBI] 0.000949185
AFP [NCBI] 4.92978e-05
PAX3 [NCBI] 3.53415e-05
ACHE [NCBI] 1.62223e-05
UMOD [NCBI] 1.29329e-05
ALDH1A2 [NCBI] 1.28049e-05
MARCKSL1 [NCBI] 1.22713e-05
DLL3 [NCBI] 1.11388e-05
CITED2 [NCBI] 1.0917e-05
UPK1B [NCBI] 1.06303e-05
PAX1 [NCBI] 1.03101e-05
MNX1 [NCBI] 9.86275e-06
CMA1 [NCBI] 9.75381e-06
MTHFR [NCBI] 9.31252e-06
FOXC2 [NCBI] 8.4758e-06
MARCKS [NCBI] 7.98017e-06
PDGFRA [NCBI] 7.73661e-06
NOG [NCBI] 7.21084e-06
LEP [NCBI] 5.39492e-06
KRT20 [NCBI] 5.1577e-06
CST3 [NCBI] 4.28976e-06
BRCA1 [NCBI] 4.03635e-06



OMIM


 OMIM Link Information
gain		 01
chiari malformation type ii [NCBI] 0.00159179
neural tube defects [NCBI] 0.000400277
AFP [NCBI] 0.000219652
lipomyelomeningocele [NCBI] 0.000143802
velocardiofacial syndrome [NCBI] 0.000141871
caudal duplication anomaly [NCBI] 0.000121332
PAX3 [NCBI] 9.50285e-05
MLP [NCBI] 7.19248e-05
autonomic control, congenital failure of [NCBI] 7.1734e-05
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity [NCBI] 6.93565e-05
FDH [NCBI] 6.61613e-05
ACHE [NCBI] 6.53473e-05
CES [NCBI] 6.38082e-05
MKS1 [NCBI] 6.14849e-05
WS1 [NCBI] 6.12169e-05
DGS [NCBI] 4.36725e-05
MTHFR [NCBI] 3.9309e-05
AVP [NCBI] 8.54876e-06



Database Center for Life Science