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MeSH keywords -> Related genes, diseases (OMIM)


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01 Femur Neck [NCBI]

Gene


 Gene Link Information
Gain		 01
BMND3 [NCBI] 0.000466155
FOP [NCBI] 0.000233805
PTH [NCBI] 0.000142218
VDR [NCBI] 0.000124638
ESR1 [NCBI] 8.08461e-05
COL1A1 [NCBI] 5.97492e-05
MS [NCBI] 5.1599e-05
TNFSF11 [NCBI] 4.12826e-05
CALCR [NCBI] 2.98901e-05
TNFRSF11A [NCBI] 2.84174e-05
TNFRSF11B [NCBI] 2.43338e-05
LRP5 [NCBI] 1.62435e-05
TNFRSF1B [NCBI] 1.35453e-05
TGFB1 [NCBI] 1.29138e-05
CYP19A1 [NCBI] 1.23107e-05
LCT [NCBI] 1.1332e-05
ACP5 [NCBI] 1.06927e-05
SHBG [NCBI] 1.03703e-05
IGF1 [NCBI] 9.50272e-06
CTSK [NCBI] 9.48303e-06
IL6 [NCBI] 7.30641e-06
RUNX2 [NCBI] 6.8582e-06
IL1RN [NCBI] 6.61996e-06
ADIPOQ [NCBI] 6.50093e-06
LEP [NCBI] 6.18625e-06
IL1B [NCBI] 5.42782e-06
CLEC2D [NCBI] 5.24299e-06
CLCN7 [NCBI] 4.99185e-06
MTRR [NCBI] 4.82843e-06
EXT1 [NCBI] 4.79145e-06
TCIRG1 [NCBI] 4.75579e-06
BGLAP [NCBI] 4.62471e-06
MEPE [NCBI] 4.53663e-06
PTHLH [NCBI] 4.52028e-06
ESRRA [NCBI] 4.45573e-06
IL1R1 [NCBI] 4.35719e-06
PRDM2 [NCBI] 4.35719e-06
ACP1 [NCBI] 4.33402e-06
GC [NCBI] 4.24638e-06
LRP6 [NCBI] 4.2053e-06
ALPL [NCBI] 4.12793e-06
PTH1R [NCBI] 3.68552e-06
CYP17A1 [NCBI] 3.63912e-06
BMP2 [NCBI] 3.34418e-06
GHRL [NCBI] 3.17789e-06
GNAS [NCBI] 3.10312e-06
IGFBP1 [NCBI] 3.05838e-06
COL2A1 [NCBI] 3.05215e-06
CASR [NCBI] 3.03982e-06
RETN [NCBI] 3.00374e-06
IL1A [NCBI] 2.84621e-06
MGP [NCBI] 2.70661e-06
CALCA [NCBI] 2.5811e-06
AR [NCBI] 2.28524e-06
HFE [NCBI] 2.2735e-06
MATN1 [NCBI] 2.24927e-06
IBSP [NCBI] 1.8788e-06
SMAD3 [NCBI] 1.84249e-06
PRL [NCBI] 1.34202e-06
APOE [NCBI] 9.83428e-07
NOS3 [NCBI] 9.10654e-07
NPY [NCBI] 2.08474e-07
EGF [NCBI] 9.82926e-09



OMIM


 OMIM Link Information
gain		 01
BMND3 [NCBI] 0.00270424
spondylometaphyseal dysplasia, type a4 [NCBI] 0.0017631
PTH [NCBI] 0.000705907
VDR [NCBI] 0.000500205
RA [NCBI] 0.000483465
osteoporosis [NCBI] 0.000392922
dwarfism with tall vertebrae [NCBI] 0.000188151
spondylometaphyseal dysplasia, east african type [NCBI] 0.000148911
TNFRSF11B [NCBI] 0.000133139
legg-calve-perthes disease [NCBI] 0.000124532
renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia [NCBI] 0.00011741
BMND1 [NCBI] 0.000107034
three m syndrome [NCBI] 0.00010301
spondyloepimetaphyseal dysplasia, strudwick type [NCBI] 9.63776e-05
AIS [NCBI] 9.55238e-05
diabetes insipidus, neurohypophyseal type [NCBI] 8.6562e-05
CACP [NCBI] 8.45733e-05
growth hormone insensitivity syndrome [NCBI] 7.93538e-05
vitamin d-dependent rickets, type ii [NCBI] 6.59379e-05
FOP [NCBI] 6.0745e-05
APS1 [NCBI] 5.3308e-05
SDS [NCBI] 5.05378e-05
ESR1 [NCBI] 4.75103e-05
CD [NCBI] 3.94555e-05
SLE [NCBI] 3.84086e-05
SHBG [NCBI] 3.82818e-05
NPPB [NCBI] 3.60973e-05
TCIRG1 [NCBI] 3.01992e-05
GHRHR [NCBI] 2.96479e-05
MFS [NCBI] 2.62263e-05
CTSK [NCBI] 2.56868e-05
PTHR1 [NCBI] 2.4831e-05
TNFRSF1B [NCBI] 2.38313e-05
CYP19A1 [NCBI] 1.95998e-05
BMP2 [NCBI] 1.76344e-05
LCT [NCBI] 1.72655e-05
PTHLH [NCBI] 1.69469e-05
ACP5 [NCBI] 1.66478e-05
temporal arteritis [NCBI] 1.52254e-05
EGF [NCBI] 1.51043e-05
LEP [NCBI] 1.49416e-05
BGLAP [NCBI] 1.32796e-05
AD [NCBI] 7.29834e-06
AR [NCBI] 3.27504e-06
NPY [NCBI] 2.01601e-06
APOE [NCBI] 1.13943e-06
CF [NCBI] 4.26534e-07
PRL [NCBI] 1.82068e-08



Database Center for Life Science