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MeSH keywords -> Related genes, diseases (OMIM)


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01 Dental Caries [NCBI]


Gene


Gene Link Information
Gain
01
FOP [NCBI] 0.000395926
DSPP [NCBI] 4.39152e-05
MS [NCBI] 4.22463e-05
NES [NCBI] 3.31865e-05
BMP4 [NCBI] 2.32231e-05
MUC7 [NCBI] 2.12059e-05
PDLIM7 [NCBI] 1.90816e-05
TFIP11 [NCBI] 1.68316e-05
CCR6 [NCBI] 1.63318e-05
CCL20 [NCBI] 1.63318e-05
PRH2 [NCBI] 1.44511e-05
CA6 [NCBI] 1.35527e-05
TUFT1 [NCBI] 1.35527e-05
GDF11 [NCBI] 1.29693e-05
PLXNB3 [NCBI] 1.25356e-05
AMY1A [NCBI] 1.25356e-05
TGFBR1 [NCBI] 1.23078e-05
CST1 [NCBI] 1.19024e-05
PRH1 [NCBI] 1.16564e-05
CST4 [NCBI] 1.10783e-05
ENAM [NCBI] 1.05241e-05
MUC5B [NCBI] 1.03023e-05
AMBN [NCBI] 1.02013e-05
AMELX [NCBI] 1.00157e-05
HLA-DQB1 [NCBI] 9.93095e-06
LCN1 [NCBI] 9.92985e-06
MMP20 [NCBI] 9.84815e-06
PRKCSH [NCBI] 9.77016e-06
MYO6 [NCBI] 9.36475e-06
KLK11 [NCBI] 9.19316e-06
HLA-DRB1 [NCBI] 8.69987e-06
TGFB3 [NCBI] 8.52575e-06
RECK [NCBI] 8.2856e-06
GALNS [NCBI] 8.22277e-06
DMBT1 [NCBI] 8.07511e-06
ALPL [NCBI] 7.96555e-06
CDH2 [NCBI] 7.93922e-06
NPY [NCBI] 7.52461e-06
DEFB1 [NCBI] 7.27674e-06
GJA1 [NCBI] 7.2417e-06
NGFR [NCBI] 6.59979e-06
DEFB4 [NCBI] 6.55296e-06
GHR [NCBI] 6.50739e-06
MGP [NCBI] 6.38806e-06
TGFB2 [NCBI] 6.04782e-06
IBSP [NCBI] 6.04782e-06
CXCL10 [NCBI] 5.98072e-06
PAX3 [NCBI] 5.76501e-06
ADM [NCBI] 5.72925e-06
MBL2 [NCBI] 5.52942e-06
MMP13 [NCBI] 5.26849e-06
CXCR3 [NCBI] 4.98783e-06
LAMB3 [NCBI] 4.88259e-06
F8 [NCBI] 4.77571e-06
CDH1 [NCBI] 4.67537e-06
BMP2 [NCBI] 4.30532e-06
TLR2 [NCBI] 4.28754e-06
TNFRSF11B [NCBI] 3.75996e-06
TGFB1 [NCBI] 2.20287e-06
PCNA [NCBI] 1.80204e-06
CFTR [NCBI] 1.60288e-06




OMIM


OMIM Link Information
gain
01
flynn-aird syndrome [NCBI] 0.00129156
curly hair-acral keratoderma-caries syndrome [NCBI] 0.00129156
johnson neuroectodermal syndrome [NCBI] 0.000938013
ALSG [NCBI] 0.000183236
erythema of acral regions [NCBI] 0.000127818
DSPP [NCBI] 0.000116063
FOP [NCBI] 0.000105792
acrofacial dysostosis, catania type [NCBI] 0.000105351
dyskeratosis congenita, autosomal recessive [NCBI] 9.13729e-05
GDF11 [NCBI] 7.8499e-05
dyskeratosis congenita, autosomal dominant [NCBI] 7.51743e-05
dentinogenesis imperfecta, shields type iii [NCBI] 7.51743e-05
PC1 [NCBI] 6.94982e-05
ED2 [NCBI] 6.53139e-05
immunoosseous dysplasia, schimke type [NCBI] 6.44189e-05
SMMCI [NCBI] 6.44189e-05
hypophosphatasia, adult type [NCBI] 6.44189e-05
SOST [NCBI] 6.35713e-05
DKC [NCBI] 5.22474e-05
SCS [NCBI] 5.03452e-05
FDH [NCBI] 5.03452e-05
ALPL [NCBI] 5.01662e-05
CSA [NCBI] 4.77133e-05
fructose intolerance, hereditary [NCBI] 4.63428e-05
SLS [NCBI] 4.09525e-05
NGFR [NCBI] 3.92901e-05
SDS [NCBI] 3.91145e-05
GAL [NCBI] 3.54884e-05
GHR [NCBI] 3.47314e-05
NPY [NCBI] 3.43457e-05
TLR2 [NCBI] 3.4029e-05
CF [NCBI] 3.34686e-05
ADM [NCBI] 3.21217e-05
GJA1 [NCBI] 3.15807e-05
SLE [NCBI] 2.9748e-05
MBL2 [NCBI] 2.80904e-05
WBS [NCBI] 2.70323e-05
RA [NCBI] 2.55535e-05
dystrophia myotonica 1 [NCBI] 2.45475e-05
TNFRSF11B [NCBI] 1.90281e-05
FA [NCBI] 1.20313e-05
PWS [NCBI] 9.95466e-06
lymphoma, non-hodgkin, familial [NCBI] 8.22473e-06
PCNA [NCBI] 6.40197e-06
thrombocytopenic purpura, autoimmune [NCBI] 3.82723e-06
VEGF [NCBI] 4.33511e-07




Database Center for Life Science