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MeSH keywords -> Related genes, diseases (OMIM)


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01 Bone Diseases, Metabolic [NCBI]


Gene


Gene Link Information
Gain
01
AIS [NCBI] 0.000887595
PTH [NCBI] 0.000687828
TNFRSF11B [NCBI] 0.000250158
TNFSF11 [NCBI] 0.000174454
TNFRSF11A [NCBI] 0.000164101
ACP5 [NCBI] 0.000110021
NEWENTRY [NCBI] 0.000109567
VDR [NCBI] 4.254e-05
IBSP [NCBI] 2.89461e-05
COL1A1 [NCBI] 2.78936e-05
BMP2 [NCBI] 2.02075e-05
FGF23 [NCBI] 1.94177e-05
SOST [NCBI] 1.52016e-05
PTHLH [NCBI] 1.17232e-05
IGF1 [NCBI] 1.05643e-05
SLC30A5 [NCBI] 1.04986e-05
LEPRE1 [NCBI] 9.91563e-06
CRTAP [NCBI] 9.91563e-06
NOG [NCBI] 9.54076e-06
AR [NCBI] 9.35644e-06
ACP2 [NCBI] 9.13711e-06
MGP [NCBI] 9.12296e-06
MGAT2 [NCBI] 8.38991e-06
IL1RN [NCBI] 8.15064e-06
VPS33B [NCBI] 7.87207e-06
IGFBP3 [NCBI] 7.40488e-06
HAX1 [NCBI] 6.80286e-06
LRP6 [NCBI] 6.65123e-06
IL1A [NCBI] 6.64814e-06
SEMA3B [NCBI] 6.58022e-06
BGLAP [NCBI] 6.44658e-06
CALCR [NCBI] 6.26408e-06
FHL2 [NCBI] 6.2074e-06
LEP [NCBI] 6.01868e-06
GREM1 [NCBI] 5.94951e-06
NFATC2 [NCBI] 5.85651e-06
IFNG [NCBI] 5.80404e-06
IL6 [NCBI] 5.65286e-06
P2RX7 [NCBI] 5.64439e-06
ATP8B1 [NCBI] 5.49217e-06
PRDM2 [NCBI] 5.3196e-06
NOV [NCBI] 5.2553e-06
LRP5 [NCBI] 5.22406e-06
ADAM10 [NCBI] 5.0205e-06
HAPLN1 [NCBI] 5.0205e-06
ALPL [NCBI] 4.9404e-06
BMP6 [NCBI] 4.91454e-06
CTGF [NCBI] 4.82052e-06
SQSTM1 [NCBI] 4.65414e-06
GH1 [NCBI] 4.54824e-06
SLC12A3 [NCBI] 4.46821e-06
CASP6 [NCBI] 4.37343e-06
ESR1 [NCBI] 4.35522e-06
COL1A2 [NCBI] 4.33701e-06
WNT1 [NCBI] 4.31911e-06
DKK1 [NCBI] 4.23247e-06
PHEX [NCBI] 4.1343e-06
IL1B [NCBI] 4.11415e-06
COL3A1 [NCBI] 4.10287e-06
RUNX2 [NCBI] 3.81859e-06
PXN [NCBI] 3.73004e-06
SOX9 [NCBI] 3.61163e-06
CD40LG [NCBI] 3.60027e-06
GHR [NCBI] 3.52297e-06
IGFBP1 [NCBI] 3.51223e-06
FGF2 [NCBI] 3.37907e-06
SREBF1 [NCBI] 3.23852e-06
CASP7 [NCBI] 3.20313e-06
PTGES2 [NCBI] 3.13474e-06
IRS2 [NCBI] 3.10987e-06
CYP19A1 [NCBI] 2.90291e-06
BMP4 [NCBI] 2.87456e-06
ESR2 [NCBI] 2.806e-06
FABP7 [NCBI] 2.74692e-06
IL6ST [NCBI] 2.73412e-06
LDLR [NCBI] 2.1269e-06
MS [NCBI] 2.11799e-06
INS [NCBI] 2.0903e-06
WAS [NCBI] 2.03147e-06
RAG1 [NCBI] 2.03147e-06
CYP1A1 [NCBI] 1.95334e-06
ENG [NCBI] 1.79406e-06
FGFR3 [NCBI] 1.7021e-06
ATM [NCBI] 1.69915e-06
CTSL1 [NCBI] 1.65576e-06
PTK2 [NCBI] 1.51403e-06
TGFB1 [NCBI] 1.45106e-06
IRS1 [NCBI] 1.41755e-06
LIF [NCBI] 1.26469e-06
PRL [NCBI] 9.26703e-07
VIP [NCBI] 8.17762e-07
APOE [NCBI] 8.06091e-07
APC [NCBI] 7.90892e-07
CASP3 [NCBI] 6.26395e-07
HRAS [NCBI] 6.06454e-07
TNFSF10 [NCBI] 4.39618e-07
HGF [NCBI] 2.64558e-07
CTNNB1 [NCBI] 1.62128e-07
EGF [NCBI] 1.21756e-07
TNF [NCBI] 2.15101e-08
CFTR [NCBI] 2.67605e-10




OMIM


OMIM Link Information
gain
01
PTH [NCBI] 0.00252486
HBD [NCBI] 0.0024927
IS1 [NCBI] 0.00183074
natural killer cell deficiency, familial isolated [NCBI] 0.000847142
megalocornea-mental retardation syndrome [NCBI] 0.000539786
DBQD [NCBI] 0.000525644
TNFRSF11B [NCBI] 0.000522139
BGLAP [NCBI] 0.000493346
HEPOD [NCBI] 0.000200868
shprintzen-goldberg craniosynostosis syndrome [NCBI] 0.000142199
ACP5 [NCBI] 0.000118126
xanthinuria, type ii [NCBI] 0.000113208
osteopenia and sparse hair [NCBI] 0.000113208
RA [NCBI] 0.000100954
LEPRE1 [NCBI] 9.81544e-05
VDR [NCBI] 9.34716e-05
osteogenesis imperfecta, type iib [NCBI] 8.22828e-05
bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features [NCBI] 8.22828e-05
osteogenesis imperfecta, type vii [NCBI] 7.67894e-05
satoyoshi syndrome [NCBI] 7.67894e-05
osteogenesis imperfecta, type viii [NCBI] 7.27084e-05
CD [NCBI] 6.67799e-05
GDD [NCBI] 6.4451e-05
RUNX2 [NCBI] 6.25909e-05
weill-marchesani syndrome, autosomal recessive [NCBI] 6.06443e-05
NSHPT [NCBI] 5.62372e-05
xanthinuria, type i [NCBI] 5.27934e-05
chondrodysplasia punctata, autosomal dominant [NCBI] 5.27934e-05
SLC30A5 [NCBI] 5.19898e-05
SP7 [NCBI] 5.19898e-05
osteoporosis, juvenile [NCBI] 5.17945e-05
hypophosphatasia, adult type [NCBI] 4.99693e-05
SCN1 [NCBI] 4.91306e-05
FGF23 [NCBI] 4.87267e-05
CRTAP [NCBI] 4.68017e-05
SIAH1 [NCBI] 4.34371e-05
hypophosphatasia, infantile [NCBI] 3.92211e-05
PPIB [NCBI] 3.89504e-05
growth hormone insensitivity syndrome [NCBI] 3.87979e-05
IL6ST [NCBI] 3.72992e-05
CALCR [NCBI] 3.46549e-05
IFNB1 [NCBI] 3.46549e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 3.41672e-05
MMP14 [NCBI] 3.35614e-05
SOST [NCBI] 3.35614e-05
mucolipidosis ii [NCBI] 3.27115e-05
PAX5 [NCBI] 3.16873e-05
CD44 [NCBI] 3.08713e-05
CF [NCBI] 3.07674e-05
EGF [NCBI] 3.03598e-05
KLK3 [NCBI] 2.83457e-05
SLC12A3 [NCBI] 2.81635e-05
FOS [NCBI] 2.75917e-05
GAD2 [NCBI] 2.75917e-05
CCD [NCBI] 2.63306e-05
LRP5 [NCBI] 2.60584e-05
RPS6KA3 [NCBI] 2.47404e-05
AHO [NCBI] 2.39061e-05
APS1 [NCBI] 2.3327e-05
GLB1 [NCBI] 2.13486e-05
MAS [NCBI] 2.1116e-05
IRS1 [NCBI] 2.10694e-05
DBA [NCBI] 2.0997e-05
CYP19A1 [NCBI] 2.02804e-05
MDD [NCBI] 2.00427e-05
coproporphyria [NCBI] 2.00321e-05
PMD [NCBI] 1.97567e-05
TNF [NCBI] 1.92376e-05
SMAX1 [NCBI] 1.8434e-05
TNFSF11 [NCBI] 1.58315e-05
ESR1 [NCBI] 1.45726e-05
IHH [NCBI] 1.44439e-05
AR [NCBI] 1.0701e-05
LRP1 [NCBI] 9.71168e-06
IL6 [NCBI] 9.50914e-06
WAS [NCBI] 8.80637e-06
AKR1B1 [NCBI] 7.56149e-06
INS [NCBI] 5.53607e-06
TNFSF10 [NCBI] 5.042e-06
phenylketonuria [NCBI] 4.97968e-06
FGFR3 [NCBI] 4.85739e-06
PRL [NCBI] 4.46503e-06
temporal arteritis [NCBI] 4.40021e-06
HGF [NCBI] 3.34271e-06
PWS [NCBI] 1.44979e-06
PTK2 [NCBI] 9.50803e-07
CFTR [NCBI] 8.96673e-07
lymphoma, non-hodgkin, familial [NCBI] 6.92463e-07
PTHLH [NCBI] 6.633e-07
PPARA [NCBI] 3.73141e-07
VIP [NCBI] 3.24098e-07
TNFSF6 [NCBI] 2.16641e-07
SLE [NCBI] 3.3853e-10




Database Center for Life Science