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MeSH keywords -> Related genes, diseases (OMIM)


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01 Osteochondritis [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 5.28348e-05
ASPN [NCBI] 1.22815e-05
LTF [NCBI] 1.10095e-05
GLI3 [NCBI] 1.02252e-05
PTGS2 [NCBI] 9.84903e-06
NOG [NCBI] 9.31688e-06
COMP [NCBI] 8.7694e-06
CTSL1 [NCBI] 7.16464e-06
PTH [NCBI] 3.68301e-06
TNF [NCBI] 2.49497e-06



OMIM


 OMIM Link Information
gain		 01
OD [NCBI] 0.0047277
osteoarthropathy of fingers, familial [NCBI] 0.00276787
kyphomelic dysplasia [NCBI] 0.000555363
legg-calve-perthes disease [NCBI] 0.000442599
osteochondrosis deformans tibiae, familial infantile type [NCBI] 0.000412382
campomelic dysplasia [NCBI] 0.000143045
nathalie syndrome [NCBI] 0.000136591
tibia vara [NCBI] 0.000114122
kniest-like dysplasia with pursed lips and ectopia lentis [NCBI] 0.000114122
IHH [NCBI] 0.000113887
ruvalcaba syndrome [NCBI] 9.00744e-05
KCS [NCBI] 8.23042e-05
HSPG2 [NCBI] 7.00104e-05
TRPS2 [NCBI] 5.97448e-05
SJS1 [NCBI] 5.86494e-05
LWD [NCBI] 5.83004e-05
CHH [NCBI] 5.14123e-05
COMP [NCBI] 3.92598e-05
RA [NCBI] 1.84051e-05
PWS [NCBI] 1.69841e-05
PTH [NCBI] 1.05376e-05
SLE [NCBI] 9.43832e-06
TNF [NCBI] 5.89603e-06



Database Center for Life Science