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MeSH keywords -> Related genes, diseases (OMIM)


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01 Arnold-Chiari Malformation [NCBI]

Gene


 Gene Link Information
Gain		 01
AIS [NCBI] 0.000572277
HFM [NCBI] 0.000193108
PAX3 [NCBI] 2.03915e-05
GFAP [NCBI] 1.2732e-05
PAX2 [NCBI] 1.00082e-05
VIM [NCBI] 9.95259e-06
FGFR2 [NCBI] 9.21896e-06
FGFR3 [NCBI] 7.62409e-06
CFTR [NCBI] 4.48986e-06



OMIM


 OMIM Link Information
gain		 01
chiari malformation type i [NCBI] 0.0186857
syringomyelia, isolated [NCBI] 0.00199086
chiari malformation type ii [NCBI] 0.000907885
IS1 [NCBI] 0.000372938
NS1 [NCBI] 0.000222768
DWS [NCBI] 0.000187992
HFM [NCBI] 0.000100812
papillorenal syndrome [NCBI] 8.25826e-05
ABS [NCBI] 7.41402e-05
OKS [NCBI] 7.41402e-05
autonomic control, congenital failure of [NCBI] 7.30808e-05
FDH [NCBI] 6.75057e-05
PAX2 [NCBI] 5.7247e-05
ACADS [NCBI] 5.68152e-05
PAX3 [NCBI] 4.74319e-05
GFAP [NCBI] 3.97289e-05
FGFR2 [NCBI] 3.95255e-05
GHRH [NCBI] 3.45639e-05
CFTR [NCBI] 1.90616e-05
CJD [NCBI] 1.75802e-05
CF [NCBI] 9.9205e-06
RA [NCBI] 4.73194e-06



Database Center for Life Science