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MeSH keywords -> Related genes, diseases (OMIM)


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01 Foot [NCBI]

Gene


 Gene Link Information
Gain		 01
SHFM2 [NCBI] 0.000320909
WDM [NCBI] 0.000303292
MS [NCBI] 0.000256993
FOP [NCBI] 0.000187914
FGF23 [NCBI] 2.04289e-05
NGF [NCBI] 1.5362e-05
TNF [NCBI] 1.22346e-05
ATF3 [NCBI] 9.71229e-06
MITF [NCBI] 8.06966e-06
CS [NCBI] 7.45326e-06
OPRL1 [NCBI] 6.69063e-06
SPRR1A [NCBI] 6.42365e-06
SLC39A4 [NCBI] 6.26311e-06
SPRR1B [NCBI] 5.84505e-06
CLCN7 [NCBI] 5.75193e-06
BSCL2 [NCBI] 5.55122e-06
TH [NCBI] 5.31916e-06
PKP1 [NCBI] 5.29593e-06
NSD1 [NCBI] 5.24115e-06
DKK3 [NCBI] 5.11607e-06
NPY [NCBI] 5.01689e-06
HLA-DMA [NCBI] 5.00496e-06
HLA-DMB [NCBI] 4.96376e-06
ALCAM [NCBI] 4.84951e-06
ATF1 [NCBI] 4.83168e-06
FCGR2B [NCBI] 4.46613e-06
SOX10 [NCBI] 4.28747e-06
PRLR [NCBI] 4.02041e-06
DKK1 [NCBI] 3.95989e-06
AGXT2L1 [NCBI] 3.92387e-06
CHI3L1 [NCBI] 3.90982e-06
CD163 [NCBI] 3.75521e-06
ADAR [NCBI] 3.74926e-06
PITX1 [NCBI] 3.73164e-06
VEGFA [NCBI] 3.72053e-06
DSP [NCBI] 3.69733e-06
MPO [NCBI] 3.64656e-06
HP [NCBI] 3.60613e-06
COMP [NCBI] 3.50869e-06
HLA-DRB1 [NCBI] 3.38675e-06
NFE2L2 [NCBI] 3.37454e-06
VIP [NCBI] 3.18443e-06
PAM [NCBI] 3.10441e-06
CRH [NCBI] 3.08922e-06
PMP22 [NCBI] 3.00829e-06
MATN1 [NCBI] 2.98907e-06
PF4 [NCBI] 2.94395e-06
ENG [NCBI] 2.87394e-06
PARK2 [NCBI] 2.85013e-06
SHH [NCBI] 2.69822e-06
COMT [NCBI] 2.62862e-06
SPI1 [NCBI] 2.58847e-06
HMOX1 [NCBI] 2.42185e-06
PRKCB [NCBI] 2.22195e-06
AHR [NCBI] 2.159e-06
IL6 [NCBI] 2.10328e-06
CD86 [NCBI] 2.03688e-06
IL1RN [NCBI] 1.87839e-06
LIF [NCBI] 1.58364e-06
NOS3 [NCBI] 1.57779e-06
STAT3 [NCBI] 1.43751e-06
CTNNB1 [NCBI] 1.37909e-06
MBP [NCBI] 1.28576e-06
CHAT [NCBI] 1.28576e-06
BDNF [NCBI] 1.04438e-06
EGFR [NCBI] 8.76929e-07
ACHE [NCBI] 8.67447e-07
PRL [NCBI] 7.20287e-07
EGF [NCBI] 1.59773e-07



OMIM


 OMIM Link Information
gain		 01
RA [NCBI] 0.00125802
myopathy, distal, with onset in infancy [NCBI] 0.00121566
upington disease [NCBI] 0.00121566
camptobrachydactyly [NCBI] 0.00121566
fingerprints, absence of [NCBI] 0.000905644
dermal ridges-off-the-end [NCBI] 0.000905644
osteodysplasia, familial, anderson type [NCBI] 0.000905644
dyschromatosis universalis hereditaria [NCBI] 0.000905644
SHFM1 [NCBI] 0.000863573
spondylometaphyseal dysplasia, corner fracture type [NCBI] 0.000789241
wieacker syndrome [NCBI] 0.000789241
callosities, hereditary painful [NCBI] 0.000789241
spondyloepiphyseal dysplasia tarda, autosomal dominant [NCBI] 0.000789241
keratolytic winter erythema [NCBI] 0.000713991
SHFM2 [NCBI] 0.000713991
dermal ridges, patternless [NCBI] 0.000713991
hereditary motor and sensory neuropathy v [NCBI] 0.000614097
IH [NCBI] 0.000614097
peeling skin syndrome [NCBI] 0.000577513
acrodysostosis [NCBI] 0.000577513
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.0005192
WDM [NCBI] 0.000495203
mohr syndrome [NCBI] 0.000495203
osteolysis, hereditary, of carpal bones with nephropathy [NCBI] 0.000495203
SHFLD1 [NCBI] 0.000473712
varadi-papp syndrome [NCBI] 0.000436535
proteus syndrome [NCBI] 0.000333372
coffin-siris syndrome [NCBI] 0.000314449
TCC [NCBI] 0.000276189
EEC1 [NCBI] 0.000274339
pfeiffer syndrome [NCBI] 0.000272301
AOS [NCBI] 0.000219674
SPDA1 [NCBI] 0.000183186
SYM1 [NCBI] 0.00016853
osteolysis, hereditary multicentric [NCBI] 0.00016501
ulnar hypoplasia with lobster-claw deformity of feet [NCBI] 0.00016501
peroneal nerve, accessory deep [NCBI] 0.00016501
metachondromatosis [NCBI] 0.00016501
eiken skeletal dysplasia [NCBI] 0.00016501
acrorenal syndrome [NCBI] 0.00016501
symphalangism with multiple anomalies of hands and feet [NCBI] 0.00016501
LRS1 [NCBI] 0.000156994
BCNS [NCBI] 0.000134649
acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia [NCBI] 0.000125816
peeling skin syndrome, acral type [NCBI] 0.000125816
tetramelic monodactyly [NCBI] 0.000125816
S PEAK SYNDROME [NCBI] 0.000125816
dysplasia epiphysealis hemimelica [NCBI] 0.000125816
dermal ridges, nelson syndrome [NCBI] 0.000125816
brachydactyly, preaxial, with hallux varus and thumb abduction [NCBI] 0.000111075
melorheostosis [NCBI] 0.000111075
ankylosing vertebral hyperostosis with tylosis [NCBI] 0.000111075
acrogeria, gottron type [NCBI] 0.000111075
SHFM4 [NCBI] 0.000111075
ectrodactyly [NCBI] 0.000111075
SLE [NCBI] 0.00010163
roussy-levy hereditary areflexic dystasia [NCBI] 0.000101531
spondyloperipheral dysplasia [NCBI] 9.4456e-05
DA1 [NCBI] 8.88347e-05
ruvalcaba syndrome [NCBI] 8.88347e-05
OPTA2 [NCBI] 8.41741e-05
erythermalgia, primary [NCBI] 8.41741e-05
TD2 [NCBI] 8.01963e-05
osseous heteroplasia, progressive [NCBI] 8.01963e-05
lymphedema, hereditary, i [NCBI] 7.6729e-05
buschke-ollendorff syndrome [NCBI] 7.3658e-05
BDB1 [NCBI] 7.3658e-05
myopathy, myosin storage [NCBI] 7.3658e-05
OPD1 [NCBI] 7.09036e-05
hand-foot-uterus syndrome [NCBI] 7.09036e-05
SYNS1 [NCBI] 7.09036e-05
PDP [NCBI] 7.09036e-05
DMC [NCBI] 6.8408e-05
dyschromatosis symmetrica hereditaria 1 [NCBI] 6.61278e-05
FMD [NCBI] 6.40298e-05
tibial muscular dystrophy, tardive [NCBI] 6.2088e-05
chondrodysplasia punctata, autosomal dominant [NCBI] 6.2088e-05
camurati-engelmann disease [NCBI] 6.2088e-05
apert syndrome [NCBI] 6.2088e-05
HSAN1 [NCBI] 5.8593e-05
SPG3A [NCBI] 5.7009e-05
ATF3 [NCBI] 5.55837e-05
HCH [NCBI] 5.41095e-05
CRH [NCBI] 5.03117e-05
EBR1 [NCBI] 5.03052e-05
ACLS [NCBI] 4.80594e-05
DA2A [NCBI] 4.6003e-05
SLC39A4 [NCBI] 4.11115e-05
CD69 [NCBI] 4.11115e-05
TGM5 [NCBI] 4.11115e-05
IHH [NCBI] 3.9582e-05
FOP [NCBI] 3.91969e-05
TBX4 [NCBI] 3.84594e-05
NGFB [NCBI] 3.69065e-05
ADAR [NCBI] 3.65284e-05
CRMO [NCBI] 3.57803e-05
RSTS [NCBI] 3.57803e-05
AMC [NCBI] 3.51556e-05
PITX1 [NCBI] 3.37565e-05
TBX5 [NCBI] 3.1764e-05
TP73L [NCBI] 3.05664e-05
SLC5A7 [NCBI] 2.95415e-05
TD1 [NCBI] 2.92678e-05
PTHR1 [NCBI] 2.83707e-05
PWS [NCBI] 2.45802e-05
FRDA [NCBI] 2.36261e-05
COL2A1 [NCBI] 2.33633e-05
TGFB1 [NCBI] 2.29762e-05
TNF [NCBI] 2.26786e-05
PD [NCBI] 2.08748e-05
PRLR [NCBI] 1.99672e-05
WT1 [NCBI] 1.98642e-05
SHH [NCBI] 1.76698e-05
MG [NCBI] 1.67881e-05
fragile x mental retardation syndrome [NCBI] 1.52426e-05
PMP22 [NCBI] 1.50059e-05
HP [NCBI] 1.49287e-05
OPMD [NCBI] 1.44269e-05
COMP [NCBI] 1.39667e-05
DFSP [NCBI] 1.32865e-05
SDC2 [NCBI] 1.16163e-05
SLOS [NCBI] 1.15814e-05
GHRH [NCBI] 1.07878e-05
STAT3 [NCBI] 1.06894e-05
PF4 [NCBI] 1.0348e-05
MAG [NCBI] 9.55651e-06
TH [NCBI] 8.75538e-06
NPY [NCBI] 7.25133e-06
MJD [NCBI] 6.86789e-06
MPO [NCBI] 6.3759e-06
EGF [NCBI] 5.63606e-06
AHR [NCBI] 5.41027e-06
VIP [NCBI] 4.10547e-06
FMF [NCBI] 3.66159e-06
VEGF [NCBI] 2.97014e-06
MBP [NCBI] 8.90915e-07
CHAT [NCBI] 8.37877e-07
BDNF [NCBI] 2.24453e-07
PRL [NCBI] 8.7631e-08
ACHE [NCBI] 4.80855e-09



Database Center for Life Science