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MeSH keywords -> Related genes, diseases (OMIM)


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01 Knee [NCBI]


Gene


Gene Link Information
Gain
01
BFHD [NCBI] 0.000466155
OA22 [NCBI] 0.000466155
OA21 [NCBI] 0.000466155
OA23 [NCBI] 0.000466155
GER [NCBI] 0.000102676
MS [NCBI] 5.1599e-05
ACTN3 [NCBI] 1.35343e-05
IRF6 [NCBI] 1.33961e-05
ANKH [NCBI] 1.33305e-05
COL2A1 [NCBI] 1.00724e-05
FGF23 [NCBI] 9.85684e-06
MSTN [NCBI] 9.68306e-06
MB [NCBI] 9.37531e-06
CS [NCBI] 8.51397e-06
CNTF [NCBI] 6.9736e-06
PDK2 [NCBI] 6.95277e-06
ASPN [NCBI] 6.79219e-06
IL6 [NCBI] 6.61031e-06
CNTFR [NCBI] 6.59127e-06
PRKAG3 [NCBI] 6.59127e-06
PRKAB2 [NCBI] 6.47674e-06
COL9A2 [NCBI] 6.11707e-06
PRKAG1 [NCBI] 5.88254e-06
ECM1 [NCBI] 5.76971e-06
CD68 [NCBI] 5.68656e-06
ITGA1 [NCBI] 5.24309e-06
PRKAB1 [NCBI] 5.2121e-06
PRKAA2 [NCBI] 4.91144e-06
PRKAA1 [NCBI] 4.87816e-06
CEBPD [NCBI] 4.81474e-06
F5 [NCBI] 4.74553e-06
CXCR5 [NCBI] 4.61168e-06
F2 [NCBI] 4.30522e-06
CCL5 [NCBI] 3.88653e-06
MITF [NCBI] 3.86272e-06
ALK [NCBI] 3.81304e-06
SOX9 [NCBI] 3.67101e-06
ALB [NCBI] 3.63927e-06
MATN1 [NCBI] 3.51066e-06
PF4 [NCBI] 3.46516e-06
IL1B [NCBI] 3.29518e-06
OSM [NCBI] 3.0431e-06
CCL2 [NCBI] 2.71713e-06
VDR [NCBI] 2.53444e-06
BIRC5 [NCBI] 2.40197e-06
IL1RN [NCBI] 2.38315e-06
STAT1 [NCBI] 2.21623e-06
LIF [NCBI] 2.07924e-06
STAT3 [NCBI] 1.92725e-06
NOS2 [NCBI] 1.91146e-06
AKT1 [NCBI] 1.57892e-06
PCNA [NCBI] 1.56424e-06
PTH [NCBI] 1.24546e-06
NPY [NCBI] 1.14715e-06
TNF [NCBI] 5.14628e-07




OMIM


OMIM Link Information
gain
01
corneal dystrophy, crystalline, of schnyder [NCBI] 0.00188183
PPS [NCBI] 0.00148125
arthrogryposis-like disorder [NCBI] 0.00146221
hip dysplasia, beukes type [NCBI] 0.00146221
OD [NCBI] 0.00145146
trichoscyphodysplasia [NCBI] 0.00115153
metaphyseal acroscyphodysplasia [NCBI] 0.00115153
DBQD [NCBI] 0.000735764
behcet syndrome [NCBI] 0.00061405
pena-shokeir syndrome, type i [NCBI] 0.000495203
genu valgum, st. helena familial [NCBI] 0.000375039
LRS1 [NCBI] 0.000339254
CCAL2 [NCBI] 0.000333961
osteoarthritis [NCBI] 0.00021732
hypophosphatasia, infantile [NCBI] 0.000188631
ulna metaphyseal dysplasia syndrome [NCBI] 0.000148072
carpenter syndrome [NCBI] 0.000133285
EDM2 [NCBI] 0.000133285
ankylosing vertebral hyperostosis with tylosis [NCBI] 0.000133285
osteochondrosis deformans tibiae, familial infantile type [NCBI] 0.000133285
hunter-mcalpine craniosynostosis syndrome [NCBI] 0.000116575
ruvalcaba syndrome [NCBI] 0.000110908
noonan-like/multiple giant cell lesion syndrome [NCBI] 0.000106201
fibromatosis, juvenile hyaline [NCBI] 0.000102178
osseous heteroplasia, progressive [NCBI] 0.000102178
ANKH [NCBI] 0.000100704
RA [NCBI] 0.000100143
SEDT [NCBI] 9.55481e-05
EDM1 [NCBI] 9.02066e-05
WGN1 [NCBI] 9.02066e-05
COFS1 [NCBI] 8.57369e-05
CACP [NCBI] 8.37493e-05
CMDD [NCBI] 8.01629e-05
STL1 [NCBI] 7.69962e-05
FMF [NCBI] 6.66169e-05
RTS [NCBI] 6.07389e-05
AMC [NCBI] 5.56275e-05
VWS [NCBI] 5.43375e-05
NPS [NCBI] 5.37164e-05
MB [NCBI] 5.33809e-05
SDS [NCBI] 4.9754e-05
ASPN [NCBI] 4.92882e-05
COL9A2 [NCBI] 4.78387e-05
ACH [NCBI] 4.21774e-05
contractural arachnodactyly, congenital [NCBI] 3.87232e-05
CNTF [NCBI] 3.58619e-05
COL2A1 [NCBI] 3.14748e-05
DFSP [NCBI] 3.07362e-05
SLE [NCBI] 2.85314e-05
ALK [NCBI] 2.35842e-05
NF1 [NCBI] 2.28342e-05
PF4 [NCBI] 1.806e-05
CVID [NCBI] 1.59731e-05
VDR [NCBI] 1.16761e-05
CEACAM5 [NCBI] 6.97114e-06
PCNA [NCBI] 5.0143e-06
PTH [NCBI] 3.0975e-06
PD [NCBI] 2.73066e-06
NPY [NCBI] 2.50024e-06




Database Center for Life Science