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MeSH keywords -> Related genes, diseases (OMIM)


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01 Fractures, Spontaneous [NCBI]

Gene


 Gene Link Information
Gain		 01
PTH [NCBI] 7.75587e-05
TNFRSF11B [NCBI] 6.73095e-05
CASR [NCBI] 2.43476e-05
COL1A1 [NCBI] 2.28365e-05
PSTPIP2 [NCBI] 1.43094e-05
PSTPIP1 [NCBI] 1.05051e-05
SLC5A2 [NCBI] 1.03825e-05
TNFRSF11A [NCBI] 1.01399e-05
ESR1 [NCBI] 9.88388e-06
KLF10 [NCBI] 9.78831e-06
TNFSF11 [NCBI] 9.66846e-06
CLCN7 [NCBI] 9.48258e-06
DMP1 [NCBI] 9.107e-06
KL [NCBI] 9.0517e-06
CA2 [NCBI] 8.79921e-06
MTPN [NCBI] 7.93389e-06
ALPL [NCBI] 7.82436e-06
GAA [NCBI] 7.06648e-06
IBSP [NCBI] 5.90773e-06
DPP4 [NCBI] 5.87388e-06
CYP19A1 [NCBI] 5.71419e-06
FGF23 [NCBI] 5.35886e-06
UCP3 [NCBI] 5.12935e-06
FLT3 [NCBI] 4.22259e-06
BMP2 [NCBI] 4.16818e-06
SHBG [NCBI] 3.97521e-06
PTHLH [NCBI] 3.4194e-06
VDR [NCBI] 3.22525e-06
IL1RN [NCBI] 2.50232e-06
PTGS2 [NCBI] 1.14451e-06



OMIM


 OMIM Link Information
gain		 01
osteodysplasia, familial, anderson type [NCBI] 0.00102023
spondylometaphyseal dysplasia, corner fracture type [NCBI] 0.000938013
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.000672411
ACG1A [NCBI] 0.000661222
PTH [NCBI] 0.000247239
hypophosphatasia, adult type [NCBI] 0.000159075
osteogenesis imperfecta, type i [NCBI] 0.000109429
genochondromatosis [NCBI] 0.00010855
TNFRSF11B [NCBI] 0.000104112
bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features [NCBI] 0.000100073
OPTB5 [NCBI] 8.45096e-05
ACG2 [NCBI] 7.26836e-05
OPTA2 [NCBI] 7.26836e-05
paget disease, juvenile [NCBI] 7.0453e-05
osteogenesis imperfecta, type iv [NCBI] 6.67501e-05
osteogenesis imperfecta, type iii [NCBI] 6.44447e-05
niemann-pick disease, type b [NCBI] 6.30739e-05
hyperoxaluria, primary, type i [NCBI] 5.75738e-05
hypophosphatasia, infantile [NCBI] 5.66701e-05
SJS1 [NCBI] 5.31414e-05
CLCN7 [NCBI] 5.10084e-05
IL1RN [NCBI] 4.68441e-05
IL1B [NCBI] 4.57718e-05
TD1 [NCBI] 4.44626e-05
SMPD1 [NCBI] 4.31157e-05
menkes disease [NCBI] 4.29288e-05
AHO [NCBI] 4.07231e-05
ATP7A [NCBI] 3.93038e-05
CYP19A1 [NCBI] 3.93038e-05
B2M [NCBI] 3.52641e-05
COL1A1 [NCBI] 2.9718e-05
BGLAP [NCBI] 2.76933e-05
RA [NCBI] 2.3696e-05
PTHLH [NCBI] 1.43307e-05
CD [NCBI] 1.25969e-05
SHBG [NCBI] 1.24746e-05
VDR [NCBI] 1.04407e-05
SLE [NCBI] 3.80987e-07
KLK3 [NCBI] 2.64218e-07



Database Center for Life Science