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01 Anodontia [NCBI]

Gene


 Gene Link Information
Gain		 01
PAX9 [NCBI] 0.000469667
HYD2 [NCBI] 0.000415947
MSX1 [NCBI] 0.00032343
ZLS [NCBI] 0.000317391
HFM [NCBI] 0.000207942
EDA [NCBI] 9.34761e-05
AXIN2 [NCBI] 5.39638e-05
IRF6 [NCBI] 4.99158e-05
BMP4 [NCBI] 2.09782e-05
EDAR [NCBI] 2.02456e-05
PITX2 [NCBI] 1.88542e-05
ZNF22 [NCBI] 1.22307e-05
SH3BP2 [NCBI] 8.62736e-06
ABCD3 [NCBI] 8.45592e-06
TGFB3 [NCBI] 7.78928e-06
DLX3 [NCBI] 7.61462e-06
FOXC1 [NCBI] 7.03038e-06
FGF4 [NCBI] 6.40722e-06
FGFR1 [NCBI] 6.19335e-06
FGF3 [NCBI] 6.09581e-06
TSC2 [NCBI] 5.88014e-06
IKBKE [NCBI] 4.63867e-06
CHUK [NCBI] 4.46789e-06
IKBKB [NCBI] 4.45779e-06
SHH [NCBI] 4.45276e-06
MMP2 [NCBI] 3.97423e-06
FGFR3 [NCBI] 3.81482e-06
TGFB1 [NCBI] 1.56959e-06



OMIM


 OMIM Link Information
gain		 01
STHAG4 [NCBI] 0.00393997
gapo syndrome [NCBI] 0.0037667
anodontia of permanent dentition [NCBI] 0.00238746
schopf-schulz-passarge syndrome [NCBI] 0.00191078
VWS [NCBI] 0.00101495
kabuki syndrome [NCBI] 0.000941848
STHAG2 [NCBI] 0.000907885
STHAG5 [NCBI] 0.000690406
STHAG3 [NCBI] 0.000654454
PAX9 [NCBI] 0.0005762
rosselli-gulienetti syndrome [NCBI] 0.000555675
MSX1 [NCBI] 0.000522439
SMMCI [NCBI] 0.000406182
STHAG1 [NCBI] 0.000404447
PCA [NCBI] 0.000401101
dupuytren contracture [NCBI] 0.000401101
ZLS [NCBI] 0.000372002
microcephaly, autosomal dominant [NCBI] 0.000372002
witkop syndrome [NCBI] 0.000282003
EEC1 [NCBI] 0.000210308
RIEG1 [NCBI] 0.000195134
apnea, obstructive sleep [NCBI] 0.000191968
ED1 [NCBI] 0.00016218
OFC1 [NCBI] 0.000150501
CPI [NCBI] 0.000149863
ectodermal dysplasia, hidrotic, autosomal recessive [NCBI] 0.000116222
teeth, congenital absence of, with taurodontia and sparse hair [NCBI] 0.000116222
facial dysmorphism, selective tooth agenesis, and choroid calcification [NCBI] 0.000116222
dermatoosteolysis, kirghizian type [NCBI] 0.000116222
hypodontia, x-linked [NCBI] 0.000116222
oligodontia-colorectal cancer syndrome [NCBI] 0.000116222
HFM [NCBI] 0.000100812
ectodermal dysplasia, trichoodontoonychial type [NCBI] 9.37621e-05
tooth malformation [NCBI] 9.37621e-05
deafness-oligodontia syndrome [NCBI] 9.37621e-05
trichodental dysplasia [NCBI] 9.37621e-05
RTS [NCBI] 9.34731e-05
epidermolysis bullosa, late-onset localized junctional, with mental retardation [NCBI] 7.97964e-05
taurodontism [NCBI] 7.97964e-05
STL3 [NCBI] 7.24611e-05
ectodermal dysplasia, anhidrotic [NCBI] 7.24611e-05
AXIN2 [NCBI] 7.01659e-05
STL2 [NCBI] 6.97591e-05
adult syndrome [NCBI] 5.92212e-05
LADD [NCBI] 5.92212e-05
LMS [NCBI] 5.68389e-05
seckel syndrome 1 [NCBI] 5.38266e-05
FMD [NCBI] 5.38266e-05
IRF6 [NCBI] 5.13588e-05
EDA [NCBI] 4.97014e-05
HSS [NCBI] 4.91211e-05
PPS [NCBI] 4.84579e-05
OFD1 [NCBI] 4.66223e-05
andersen cardiodysrhythmic periodic paralysis [NCBI] 4.60556e-05
NPHP1 [NCBI] 4.55089e-05
STL1 [NCBI] 4.13038e-05
EVC [NCBI] 4.13038e-05
SJS1 [NCBI] 3.86824e-05
FGFR1 [NCBI] 3.50884e-05
ALGS1 [NCBI] 3.21127e-05
WHS [NCBI] 2.80932e-05
IP [NCBI] 2.20017e-05
GNRH1 [NCBI] 2.16942e-05
ACP5 [NCBI] 2.04634e-05
WBS [NCBI] 1.6701e-05
PXE [NCBI] 1.47337e-05
FA [NCBI] 4.12173e-06
APC [NCBI] 8.37315e-08



Database Center for Life Science