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MeSH keywords -> Related genes, diseases (OMIM)


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01 Dental Enamel [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.000217002
MMP20 [NCBI] 7.77153e-05
AMELX [NCBI] 7.40595e-05
AMBN [NCBI] 6.91351e-05
ENAM [NCBI] 3.79175e-05
STATH [NCBI] 2.98355e-05
IBSP [NCBI] 2.97749e-05
PRH1 [NCBI] 2.70983e-05
DSPP [NCBI] 1.46013e-05
DLX3 [NCBI] 1.27661e-05
EDAR [NCBI] 1.23147e-05
KLK4 [NCBI] 1.23147e-05
PTH [NCBI] 9.83418e-06
EDA [NCBI] 9.63535e-06
KRT14 [NCBI] 8.43937e-06
FGF4 [NCBI] 8.37533e-06
AMTN [NCBI] 7.64189e-06
EDARADD [NCBI] 6.53615e-06
SOSTDC1 [NCBI] 6.19908e-06
AMELY [NCBI] 5.9475e-06
WNT6 [NCBI] 5.9475e-06
CA6 [NCBI] 5.7467e-06
TGFB1 [NCBI] 5.73078e-06
HTN1 [NCBI] 5.52958e-06
SPARCL1 [NCBI] 5.48195e-06
SLIT1 [NCBI] 5.23589e-06
SOST [NCBI] 5.13241e-06
ACP5 [NCBI] 4.85329e-06
RECK [NCBI] 4.80103e-06
COL17A1 [NCBI] 4.73294e-06
CLDN7 [NCBI] 4.6289e-06
COL18A1 [NCBI] 4.49941e-06
CLDN5 [NCBI] 4.32491e-06
ERN1 [NCBI] 4.29624e-06
PMAIP1 [NCBI] 4.05865e-06
DPP7 [NCBI] 4.01516e-06
KRT5 [NCBI] 3.99411e-06
WNT1 [NCBI] 3.73065e-06
BMP6 [NCBI] 3.72271e-06
BBC3 [NCBI] 3.68395e-06
HSP90B1 [NCBI] 3.67637e-06
ANXA2 [NCBI] 3.66886e-06
WNT5A [NCBI] 3.58979e-06
EGF [NCBI] 3.56541e-06
PLAU [NCBI] 3.30429e-06
ESD [NCBI] 3.28894e-06
SERPINB5 [NCBI] 3.28894e-06
VIM [NCBI] 3.24915e-06
MGP [NCBI] 3.14307e-06
ATF2 [NCBI] 3.09617e-06
TGFB2 [NCBI] 2.91113e-06
CFTR [NCBI] 2.80881e-06
SDC1 [NCBI] 2.69383e-06
TP63 [NCBI] 2.54704e-06
JAG1 [NCBI] 2.54003e-06
BAD [NCBI] 2.5216e-06
BID [NCBI] 2.45128e-06
LAMB3 [NCBI] 2.40583e-06
BMP7 [NCBI] 2.37411e-06
SMAD2 [NCBI] 2.34911e-06
SMAD3 [NCBI] 2.26568e-06
SMAD4 [NCBI] 2.26222e-06
BMP4 [NCBI] 2.25534e-06
NOG [NCBI] 2.20365e-06
PDGFA [NCBI] 2.18918e-06
TGFBR1 [NCBI] 2.15319e-06
GAPDH [NCBI] 2.03534e-06
VDR [NCBI] 1.72925e-06
PLAUR [NCBI] 1.54539e-06
BMP2 [NCBI] 1.44147e-06
HIF1A [NCBI] 1.23872e-06
CTNNB1 [NCBI] 1.10142e-06
CASP3 [NCBI] 3.37526e-07
TNF [NCBI] 6.20751e-08



OMIM


 OMIM Link Information
gain		 01
amelogenesis imperfecta, hypoplastic type [NCBI] 0.00145218
cone-rod dystrophy and amelogenesis imperfecta [NCBI] 0.00133487
dentin dysplasia, type i [NCBI] 0.00125871
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1 [NCBI] 0.000967481
trichodentoosseous syndrome [NCBI] 0.000759456
AIHHT [NCBI] 0.000551754
dentinogenesis imperfecta, shields type iii [NCBI] 0.000453275
AIH2 [NCBI] 0.000453275
amelogenesis imperfecta, hypoplastic, and openbite malocclusion, autosomal recessive [NCBI] 0.00040953
enamel hypoplasia, hereditary localized [NCBI] 0.00040953
ENAM [NCBI] 0.000302198
DGI1 [NCBI] 0.000242909
ODDD [NCBI] 0.000214928
osteogenesis imperfecta with opalescent teeth [NCBI] 0.000204382
amelogenesis imperfecta, pigmented hypomaturation type [NCBI] 0.000204382
KLK4 [NCBI] 0.000192304
APS1 [NCBI] 0.000177324
AMELX [NCBI] 0.000168714
hearing loss, sensorineural, with enamel hypoplasia and nail defects [NCBI] 0.000165126
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation [NCBI] 0.000150321
dentin dysplasia, type ii [NCBI] 0.000123168
renal cysts and diabetes syndrome [NCBI] 0.000119128
HEPOD [NCBI] 0.000109646
periodontitis, aggressive, 1 [NCBI] 0.000104744
SOSTDC1 [NCBI] 0.000100111
mucopolysaccharidosis type iva [NCBI] 6.93369e-05
osteogenesis imperfecta, type i [NCBI] 6.29038e-05
ERP29 [NCBI] 4.99805e-05
AMBN [NCBI] 4.99805e-05
IP [NCBI] 4.69768e-05
EDARADD [NCBI] 4.6214e-05
AMTN [NCBI] 4.6214e-05
TUFT1 [NCBI] 4.6214e-05
MMP20 [NCBI] 4.6214e-05
SPP1 [NCBI] 3.78982e-05
NFE2L2 [NCBI] 3.65665e-05
ANXA2 [NCBI] 3.58469e-05
FST [NCBI] 3.30492e-05
PTH [NCBI] 3.26368e-05
ATF2 [NCBI] 2.71147e-05
DSPP [NCBI] 2.29751e-05
TS [NCBI] 2.22951e-05
VIM [NCBI] 1.95258e-05
PLAUR [NCBI] 1.91303e-05
BGLAP [NCBI] 1.74884e-05
CD [NCBI] 1.69747e-05
CFTR [NCBI] 1.2567e-05
CF [NCBI] 9.48892e-06
PTHLH [NCBI] 7.93238e-06
ACP5 [NCBI] 7.78499e-06
GAPDH [NCBI] 7.15946e-06
TNFRSF11B [NCBI] 6.71899e-06
VDR [NCBI] 5.33725e-06
SHH [NCBI] 5.3122e-06
EGF [NCBI] 3.05266e-06
TNF [NCBI] 2.73967e-06



Database Center for Life Science