Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Ossification, Heterotopic [NCBI]

Gene


 Gene Link Information
Gain		 01
FOP [NCBI] 0.00302119
BMP2 [NCBI] 0.00025351
BMP4 [NCBI] 8.64286e-05
GNAS [NCBI] 5.70094e-05
BMP7 [NCBI] 5.33102e-05
ACP5 [NCBI] 3.61245e-05
RUNX2 [NCBI] 3.20047e-05
ACVR1 [NCBI] 2.80429e-05
BMP6 [NCBI] 2.58974e-05
NOG [NCBI] 2.18284e-05
BMP5 [NCBI] 2.06388e-05
PTH [NCBI] 1.73501e-05
TGFB3 [NCBI] 1.70157e-05
BMPR1A [NCBI] 1.69421e-05
IBSP [NCBI] 1.20318e-05
GDF2 [NCBI] 1.09546e-05
SP7 [NCBI] 1.02062e-05
BAMBI [NCBI] 9.84344e-06
OGN [NCBI] 9.84344e-06
TLE1 [NCBI] 9.84344e-06
FGFR3 [NCBI] 8.98964e-06
MSX2 [NCBI] 8.87195e-06
ALX4 [NCBI] 8.78173e-06
MMP10 [NCBI] 8.46205e-06
BMP3 [NCBI] 8.39067e-06
COL6A1 [NCBI] 8.19287e-06
TNFAIP6 [NCBI] 8.0727e-06
HDAC4 [NCBI] 8.0727e-06
SMAD5 [NCBI] 8.01564e-06
GREM1 [NCBI] 7.75591e-06
LBR [NCBI] 7.7084e-06
FRZB [NCBI] 7.40847e-06
PEBP1 [NCBI] 7.12012e-06
POSTN [NCBI] 7.08729e-06
GDF5 [NCBI] 7.05508e-06
SMAD1 [NCBI] 6.99245e-06
ALPL [NCBI] 6.73613e-06
EDA [NCBI] 5.96475e-06
CD68 [NCBI] 5.53203e-06
SOX9 [NCBI] 5.37829e-06
BMPR2 [NCBI] 5.29786e-06
TIMP1 [NCBI] 5.27558e-06
PTN [NCBI] 5.26455e-06
ENPP1 [NCBI] 5.18933e-06
MGP [NCBI] 5.16846e-06
TGFB2 [NCBI] 4.83182e-06
TGFB1 [NCBI] 4.34175e-06
FGF23 [NCBI] 4.28994e-06
CD99 [NCBI] 4.13959e-06
MMP13 [NCBI] 4.06412e-06
TGFBR1 [NCBI] 3.76283e-06
F8 [NCBI] 3.58206e-06
ENG [NCBI] 3.44476e-06
SMAD4 [NCBI] 3.29918e-06
CTSL1 [NCBI] 3.28952e-06
CTGF [NCBI] 2.98264e-06
PTHLH [NCBI] 2.40627e-06
BDNF [NCBI] 1.93862e-06
TH [NCBI] 1.87463e-06
NPY [NCBI] 1.54949e-06
CTNNB1 [NCBI] 1.27925e-06
GFAP [NCBI] 1.09491e-06
PTGS2 [NCBI] 4.179e-07



OMIM


 OMIM Link Information
gain		 01
leri pleonosteosis [NCBI] 0.0030029
DBQD [NCBI] 0.00136718
pubic bone dysplasia [NCBI] 0.00109818
FOP [NCBI] 0.000819304
osseous heteroplasia, progressive [NCBI] 0.000766559
metatropic dwarfism [NCBI] 0.000647644
OD [NCBI] 0.000454472
FRNS [NCBI] 0.000412841
AHO [NCBI] 0.000280249
OPLL [NCBI] 0.000255383
HRPT2 [NCBI] 0.000136089
diaphragmatic defects, limb deficiencies, and ossification defects of skull [NCBI] 0.000119634
tracheopathia osteoplastica [NCBI] 0.000119634
coracoclavicular joint, anomalous [NCBI] 0.000119634
GNAS [NCBI] 0.000119441
ossified ear cartilages [NCBI] 9.71713e-05
metaphyseal chondrodysplasia, pena type [NCBI] 9.71713e-05
puerto rican infant hypotonia syndrome [NCBI] 9.71713e-05
BMP4 [NCBI] 9.02147e-05
TD1 [NCBI] 8.91231e-05
metaphyseal anadysplasia [NCBI] 8.86992e-05
ossified ear cartilages with mental deficiency, muscle wasting, and bony changes [NCBI] 8.86992e-05
humerospinal dysostosis [NCBI] 8.32009e-05
renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia [NCBI] 7.91149e-05
IHH [NCBI] 7.41145e-05
pseudodiastrophic dysplasia [NCBI] 7.31565e-05
keutel syndrome [NCBI] 7.31565e-05
NPPC [NCBI] 6.83427e-05
BMP5 [NCBI] 6.31438e-05
LMNB1 [NCBI] 6.31438e-05
CRS1 [NCBI] 6.26044e-05
PTH [NCBI] 6.02691e-05
SPP1 [NCBI] 6.01538e-05
enchondromatosis, multiple [NCBI] 5.8142e-05
OPD2 [NCBI] 5.8142e-05
HDAC4 [NCBI] 5.72593e-05
NPR2 [NCBI] 5.72593e-05
spondyloepimetaphyseal dysplasia, strudwick type [NCBI] 5.7198e-05
pycnodysostosis [NCBI] 5.7198e-05
hypophosphatasia, adult type [NCBI] 5.63069e-05
MCDS [NCBI] 5.63069e-05
PALS [NCBI] 5.46625e-05
SLSN1 [NCBI] 5.31732e-05
FGFR3 [NCBI] 5.1027e-05
PRG4 [NCBI] 4.98282e-05
MMP13 [NCBI] 4.98282e-05
HRPT1 [NCBI] 4.83214e-05
RA [NCBI] 4.75573e-05
CSF1 [NCBI] 4.63428e-05
BMP2 [NCBI] 4.04446e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 4.03473e-05
ALPL [NCBI] 4.00494e-05
SPARC [NCBI] 3.93038e-05
COL10A1 [NCBI] 3.93038e-05
CRMO [NCBI] 3.6521e-05
PTHLH [NCBI] 3.59388e-05
AMC [NCBI] 3.55857e-05
SDS [NCBI] 3.12914e-05
VEGF [NCBI] 2.78803e-05
ACH [NCBI] 2.69513e-05
COL1A1 [NCBI] 2.67024e-05
FGFR2 [NCBI] 2.3795e-05
PJS [NCBI] 1.82237e-05
ACP5 [NCBI] 1.39418e-05
TNFRSF11B [NCBI] 9.88517e-06
FMF [NCBI] 5.28872e-06
BDNF [NCBI] 5.10626e-06
TH [NCBI] 4.31312e-06
NPY [NCBI] 3.06782e-06
GFAP [NCBI] 1.34833e-06



Database Center for Life Science