Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Fibrous Dysplasia of Bone [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science