Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Tooth, Deciduous [NCBI]


Gene


Gene Link Information
Gain
01
HFM [NCBI] 0.000347245
ACP5 [NCBI] 2.84113e-05
DSPP [NCBI] 2.54212e-05
TNFRSF11B [NCBI] 2.39041e-05
TNFSF11 [NCBI] 2.29677e-05
TNFRSF11A [NCBI] 1.79218e-05
IBSP [NCBI] 8.28195e-06
IGFBP6 [NCBI] 6.47003e-06
MEPE [NCBI] 6.13893e-06
ALPL [NCBI] 5.72862e-06
IGF2R [NCBI] 5.55725e-06
CTSD [NCBI] 5.05935e-06
MYO6 [NCBI] 4.99458e-06
SMN2 [NCBI] 4.74962e-06
HLA-DQB1 [NCBI] 4.54178e-06
ITGAM [NCBI] 4.45477e-06
SMN1 [NCBI] 4.40898e-06
HLA-DRB1 [NCBI] 4.22359e-06
POU5F1 [NCBI] 4.2113e-06
IGF2 [NCBI] 4.11807e-06
CTSG [NCBI] 3.18306e-06
CD68 [NCBI] 2.46269e-06
PTH [NCBI] 1.52787e-06
NPY [NCBI] 1.42573e-06
EGF [NCBI] 6.98111e-07




OMIM


OMIM Link Information
gain
01
amelogenesis imperfecta, hypoplastic type [NCBI] 0.0012742
dentin dysplasia, type i [NCBI] 0.00108094
molar i reinclusion [NCBI] 0.00102443
EEC1 [NCBI] 0.000621935
DGI1 [NCBI] 0.000612831
kabuki syndrome [NCBI] 0.000526903
dentinogenesis imperfecta, shields type iii [NCBI] 0.000480476
HFM [NCBI] 0.00047322
steatocystoma multiplex with natal teeth [NCBI] 0.00042739
teeth present at birth [NCBI] 0.000373303
periodontitis, aggressive, 1 [NCBI] 0.00026942
hypophosphatasia, infantile [NCBI] 0.000240547
ACP5 [NCBI] 0.000214875
intestinal pseudoobstruction with patent ductus arteriosus and natal teeth [NCBI] 0.000213171
osteogenesis imperfecta with opalescent teeth [NCBI] 0.000213171
RSTS [NCBI] 0.000202963
CCD [NCBI] 0.000174389
PC2 [NCBI] 0.000159098
CPI [NCBI] 0.000154496
witkop syndrome [NCBI] 0.000149486
intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked [NCBI] 0.000131923
dentin dysplasia, type ii [NCBI] 0.000131923
kindler syndrome [NCBI] 0.000131923
ALSG [NCBI] 0.000115814
SMMCI [NCBI] 0.000102444
EVC [NCBI] 9.34556e-05
osteogenesis imperfecta, type iia [NCBI] 8.66877e-05
DSPP [NCBI] 7.27748e-05
osteogenesis imperfecta, type i [NCBI] 7.138e-05
TNFRSF11B [NCBI] 6.67061e-05
WHS [NCBI] 5.97643e-05
SPP1 [NCBI] 3.55125e-05
hla-d histocompatibility type [NCBI] 1.60681e-05
CF [NCBI] 8.29466e-06
PTH [NCBI] 3.69664e-06
NPY [NCBI] 3.06151e-06
EGF [NCBI] 1.64094e-07




Database Center for Life Science