Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Ankle Joint [NCBI]

Gene


 Gene Link Information
Gain		 01
AMCX5 [NCBI] 0.000466155
AIS [NCBI] 0.000166727
MS [NCBI] 5.1599e-05
MMP13 [NCBI] 1.48444e-05
PRG4 [NCBI] 1.33765e-05
GPI [NCBI] 1.17483e-05
VCAN [NCBI] 9.90395e-06
HFE [NCBI] 9.1723e-06
ACP5 [NCBI] 7.21113e-06
KCNJ12 [NCBI] 6.87819e-06
IL1RN [NCBI] 6.83356e-06
TREM2 [NCBI] 6.71979e-06
DES [NCBI] 5.70531e-06
TNF [NCBI] 5.29484e-06
C3 [NCBI] 5.2911e-06
TNFRSF1B [NCBI] 5.0348e-06
TYROBP [NCBI] 5.0348e-06
DLG1 [NCBI] 4.73295e-06
MGP [NCBI] 4.32302e-06
NGF [NCBI] 3.62324e-06
BMP7 [NCBI] 3.54054e-06
MCL1 [NCBI] 3.36528e-06
IFNGR1 [NCBI] 3.27134e-06
CTGF [NCBI] 3.03655e-06
CTSL1 [NCBI] 2.88984e-06
TLR2 [NCBI] 2.82937e-06
PTEN [NCBI] 2.78526e-06
CD68 [NCBI] 2.49299e-06



OMIM


 OMIM Link Information
gain		 01
OD [NCBI] 0.00394023
AMCX5 [NCBI] 0.0015153
RA [NCBI] 0.00109319
bruck syndrome 1 [NCBI] 0.00101143
AMCN [NCBI] 0.000812961
IS1 [NCBI] 0.00024889
CACP [NCBI] 0.000230634
metachondromatosis [NCBI] 0.000198288
megaepiphyseal dwarfism [NCBI] 0.000198288
mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones [NCBI] 0.000198288
BDB2 [NCBI] 0.000159036
TCC [NCBI] 0.000144236
por deficiency [NCBI] 0.000121822
noonan-like/multiple giant cell lesion syndrome [NCBI] 0.000117104
PDP [NCBI] 0.000103601
SYNS1 [NCBI] 0.000103601
ABS [NCBI] 8.93006e-05
PLOSL [NCBI] 8.93006e-05
PRG4 [NCBI] 8.07149e-05
CRMO [NCBI] 6.67956e-05
NPS [NCBI] 6.41651e-05
GPI [NCBI] 5.52982e-05
POR [NCBI] 4.66334e-05
TREM2 [NCBI] 4.31777e-05
NCF1 [NCBI] 4.08544e-05
ACP5 [NCBI] 3.89619e-05
FGFR2 [NCBI] 2.70344e-05
FMF [NCBI] 2.57276e-05
TLR2 [NCBI] 2.10644e-05
CTGF [NCBI] 1.54423e-05
TNF [NCBI] 1.42439e-05
TNFSF6 [NCBI] 9.19159e-06
NGFB [NCBI] 8.95255e-06
VEGF [NCBI] 3.87684e-07



Database Center for Life Science