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01 Osteosclerosis [NCBI]

Gene


 Gene Link Information
Gain		 01
OSCS [NCBI] 0.000438875
SOST [NCBI] 6.58126e-05
TNFRSF11B [NCBI] 4.59007e-05
TNFRSF11A [NCBI] 2.87023e-05
FOSL1 [NCBI] 2.85871e-05
TNFSF11 [NCBI] 2.77437e-05
FAM20C [NCBI] 1.51753e-05
TBCE [NCBI] 1.08296e-05
IL11 [NCBI] 1.00289e-05
ALPL [NCBI] 8.68767e-06
FGF8 [NCBI] 8.51117e-06
AIRE [NCBI] 7.98017e-06
DKK1 [NCBI] 7.96271e-06
NOG [NCBI] 7.31933e-06
TWIST1 [NCBI] 7.17121e-06
ATXN1 [NCBI] 6.85371e-06
PTH [NCBI] 5.8864e-06
FGFR3 [NCBI] 5.23695e-06
ACP5 [NCBI] 4.86989e-06
CDK4 [NCBI] 4.74225e-06
CD68 [NCBI] 3.47736e-06
IL1RN [NCBI] 3.30425e-06
TGFB1 [NCBI] 2.85954e-06
VEGFA [NCBI] 2.57988e-06



OMIM


 OMIM Link Information
gain		 01
OSCS [NCBI] 0.00575194
dysosteosclerosis [NCBI] 0.0020178
lateral meningocele syndrome [NCBI] 0.00148945
OSCS [NCBI] 0.00141831
CMDR [NCBI] 0.00136056
buschke-ollendorff syndrome [NCBI] 0.00105304
dentin dysplasia with sclerotic bones [NCBI] 0.00100366
RNS [NCBI] 0.000911866
pyle disease [NCBI] 0.000650784
dentin dysplasia, type i [NCBI] 0.000611315
SOST [NCBI] 0.000598984
osteomesopyknosis [NCBI] 0.000420224
camurati-engelmann disease [NCBI] 0.000270142
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus [NCBI] 0.00024631
FAM20C [NCBI] 0.000235522
TNFRSF11B [NCBI] 0.000227602
craniofacial dysostosis with diaphyseal hyperplasia [NCBI] 0.000199
CDD [NCBI] 0.000175432
GDD [NCBI] 0.000157095
hyperostosis corticalis generalisata [NCBI] 0.000142428
trichodentoosseous syndrome [NCBI] 0.000130323
pycnodysostosis [NCBI] 0.000128368
cerebellar hypoplasia with endosteal sclerosis [NCBI] 0.000114861
distal osteosclerosis [NCBI] 0.000114861
osteosclerotic chondrodysplasia, lethal, with intracellular inclusions [NCBI] 0.000114861
SLE [NCBI] 0.000101991
pyknoachondrogenesis [NCBI] 9.2402e-05
CRMO [NCBI] 8.59964e-05
MEOX1 [NCBI] 8.55726e-05
ribbing disease [NCBI] 8.39333e-05
hypophosphatemic rickets, autosomal recessive [NCBI] 7.4356e-05
BMND1 [NCBI] 7.11054e-05
desmosterolosis [NCBI] 7.11054e-05
TMEM16E [NCBI] 6.65939e-05
LTBP3 [NCBI] 6.65939e-05
lenz-majewski hyperostotic dwarfism [NCBI] 6.22847e-05
BOCD [NCBI] 6.22847e-05
SLC22A8 [NCBI] 6.07079e-05
HRD [NCBI] 6.06744e-05
KCS [NCBI] 6.06744e-05
TBCE [NCBI] 5.70453e-05
paget disease, juvenile [NCBI] 5.4425e-05
TCIRG1 [NCBI] 5.22791e-05
RA [NCBI] 4.65803e-05
OPTB1 [NCBI] 4.52907e-05
THPO [NCBI] 4.13922e-05
SEDC [NCBI] 4.08221e-05
factor vii deficiency [NCBI] 3.69309e-05
AIRE [NCBI] 3.17937e-05
SVAS [NCBI] 2.82228e-05
SDS [NCBI] 2.68305e-05
APS1 [NCBI] 2.48301e-05
MAS [NCBI] 2.25944e-05
ACE [NCBI] 2.02694e-05
WBS [NCBI] 1.55567e-05
PTHLH [NCBI] 1.46644e-05
PTH [NCBI] 7.96305e-06
VEGF [NCBI] 7.0094e-06
TS [NCBI] 4.11647e-06
lymphoma, non-hodgkin, familial [NCBI] 1.19008e-06
KLK3 [NCBI] 3.48042e-07
thrombocytopenic purpura, autoimmune [NCBI] 4.628e-09



Database Center for Life Science