Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Fibrous Dysplasia of Bone	[NCBI]

Gene	Link	Information Gain
GNAS	[NCBI]	0.000214032
FGF23	[NCBI]	5.46464e-05
PTH	[NCBI]	3.37789e-05
PHEX	[NCBI]	1.75456e-05
IBSP	[NCBI]	1.5341e-05
NPHP1	[NCBI]	8.83348e-06
POSTN	[NCBI]	8.73266e-06
MMP9	[NCBI]	4.71876e-06
BMP2	[NCBI]	4.70973e-06
IL6	[NCBI]	3.31545e-06
HIF1A	[NCBI]	2.9519e-06
VEGFA	[NCBI]	2.30173e-06
PCNA	[NCBI]	2.16262e-06

OMIM	Link	Information gain
MAS	[NCBI]	0.00331826
doughnut lesions of skull, familial	[NCBI]	0.00115589
camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases	[NCBI]	0.00092257
osteofibrous dysplasia	[NCBI]	0.000370758
GNAS	[NCBI]	0.000323482
OGD	[NCBI]	0.000169571
PTH	[NCBI]	0.000123433
camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia	[NCBI]	0.000123215
genochondromatosis	[NCBI]	0.00010075
gigantiform cementoma, familial	[NCBI]	9.22761e-05
FGFR1	[NCBI]	8.243e-05
GINGF	[NCBI]	6.61613e-05
paget disease, juvenile	[NCBI]	6.26967e-05
mulibrey nanism	[NCBI]	6.07448e-05
HRPT2	[NCBI]	5.98518e-05
NF1	[NCBI]	5.60779e-05
FOS	[NCBI]	4.97566e-05
FGF23	[NCBI]	3.94632e-05
GNRH1	[NCBI]	2.072e-05
PCNA	[NCBI]	3.52375e-06
VEGF	[NCBI]	5.93696e-08