Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Skull Neoplasms	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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