Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Cranial Fossa, Posterior [NCBI]

Gene


 Gene Link Information
Gain		 01
DWS [NCBI] 0.00036708
AIS [NCBI] 0.000166727
MS [NCBI] 5.1599e-05
GFAP [NCBI] 1.80275e-05
VHL [NCBI] 1.13708e-05
CBFB [NCBI] 7.21161e-06
TP53BP2 [NCBI] 7.129e-06
FOXC1 [NCBI] 6.71327e-06
RUNX2 [NCBI] 5.66775e-06



OMIM


 OMIM Link Information
gain		 01
chiari malformation type i [NCBI] 0.00726359
DWS [NCBI] 0.00315218
dandy-walker malformation with mental retardation, basal ganglia disease, and seizures [NCBI] 0.000864149
syringomyelia, isolated [NCBI] 0.000864149
CMDR [NCBI] 0.000763274
mohr syndrome [NCBI] 0.000642417
phace association [NCBI] 0.000179129
SACS [NCBI] 0.000175581
OKS [NCBI] 0.000145609
IS1 [NCBI] 0.000130011
VHL [NCBI] 0.000118711
GFAP [NCBI] 0.000117532
BCNS [NCBI] 0.000110663



Database Center for Life Science