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MeSH keywords -> Related genes, diseases (OMIM)


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01 Skull Neoplasms [NCBI]

Gene


 Gene Link Information
Gain		 01
GFAP [NCBI] 3.18358e-05
VIM [NCBI] 1.91071e-05
MYOM2 [NCBI] 9.77512e-06
MYOG [NCBI] 9.3765e-06
SDHB [NCBI] 9.0325e-06
SDHD [NCBI] 8.91217e-06
PCNA [NCBI] 8.65175e-06
MYOD1 [NCBI] 8.23383e-06
GNAS [NCBI] 7.45354e-06
SDC1 [NCBI] 6.64873e-06
NKX2-1 [NCBI] 6.50626e-06
VHL [NCBI] 5.37145e-06
PTHLH [NCBI] 4.99776e-06
TG [NCBI] 4.66806e-06
AR [NCBI] 3.4837e-06
AFP [NCBI] 3.34282e-06
PTH [NCBI] 2.52902e-06
TNF [NCBI] 1.43053e-06



OMIM


 OMIM Link Information
gain		 01
vascular malformation, primary intraosseous [NCBI] 0.000288957
MUC1 [NCBI] 0.00016378
osteoma of cranial vault, familial [NCBI] 0.000143802
VHL [NCBI] 0.000121955
GFAP [NCBI] 0.00011177
opitz syndrome [NCBI] 9.11242e-05
VIM [NCBI] 8.98292e-05
megalencephaly-cutis marmorata telangiectatica congenita [NCBI] 8.95027e-05
enchondromatosis, multiple [NCBI] 8.21852e-05
meningioma, familial [NCBI] 6.65275e-05
CEACAM5 [NCBI] 5.6188e-05
MAS [NCBI] 5.01789e-05
BCNS [NCBI] 4.46619e-05
GHRH [NCBI] 2.74637e-05
PCNA [NCBI] 2.23163e-05
lymphoma, non-hodgkin, familial [NCBI] 2.11769e-05
PTHLH [NCBI] 1.96163e-05
APC [NCBI] 1.57172e-05
TG [NCBI] 1.29231e-05
CRH [NCBI] 1.01257e-05
AR [NCBI] 8.33847e-06
AFP [NCBI] 6.29263e-06
PTH [NCBI] 2.90036e-06
TNF [NCBI] 3.81825e-07
VEGF [NCBI] 1.39554e-07



Database Center for Life Science