Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Mouth Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
CD68 [NCBI] 5.62831e-05
DSG3 [NCBI] 4.14953e-05
DSG1 [NCBI] 3.55685e-05
KRT13 [NCBI] 2.29119e-05
FGF7 [NCBI] 1.33652e-05
KRT4 [NCBI] 1.22011e-05
LAMB3 [NCBI] 1.14817e-05
GAS2 [NCBI] 1.1322e-05
CHD7 [NCBI] 9.29009e-06
CSPG4 [NCBI] 9.29009e-06
ITGA6 [NCBI] 8.56057e-06
KLK7 [NCBI] 8.56057e-06
CDKN1A [NCBI] 8.49238e-06
ECM1 [NCBI] 8.26746e-06
NOP2 [NCBI] 8.15577e-06
MSR1 [NCBI] 7.79934e-06
ITGAE [NCBI] 7.17086e-06
MMP12 [NCBI] 6.71317e-06
CTNNB1 [NCBI] 6.24658e-06
JUP [NCBI] 6.23303e-06
S100A4 [NCBI] 6.10997e-06
CASP7 [NCBI] 5.84136e-06
CTAG1B [NCBI] 5.81401e-06
FASLG [NCBI] 5.70281e-06
PCNA [NCBI] 5.14241e-06
NOTCH1 [NCBI] 5.139e-06
BMP7 [NCBI] 5.12699e-06
CKAP4 [NCBI] 5.12699e-06
CXCL1 [NCBI] 5.05668e-06
CTNNA1 [NCBI] 4.84187e-06
GZMB [NCBI] 4.49397e-06
TP63 [NCBI] 4.4107e-06
CCR2 [NCBI] 4.32416e-06
PON1 [NCBI] 4.19739e-06
MUC1 [NCBI] 4.09889e-06
PTGS2 [NCBI] 3.94744e-06
ACP5 [NCBI] 3.84344e-06
NME1 [NCBI] 3.75639e-06
HLA-DQB1 [NCBI] 3.47311e-06
PTHLH [NCBI] 3.23741e-06
BCL2L1 [NCBI] 2.72996e-06
TGFB1 [NCBI] 1.91059e-06
BAX [NCBI] 1.86826e-06
VWF [NCBI] 1.81993e-06
EGF [NCBI] 8.97037e-07



OMIM


 OMIM Link Information
gain		 01
dilution, pigmentary [NCBI] 0.00078076
dyskeratosis, hereditary benign intraepithelial [NCBI] 0.000687918
epidermolysis bullosa inversa dystrophica [NCBI] 0.000687918
collagenosis, familial reactive perforating [NCBI] 0.000687918
keratosis, focal palmoplantar and gingival [NCBI] 0.000687918
porokeratosis of mibelli [NCBI] 0.000555363
focal epithelial hyperplasia, oral [NCBI] 0.000482774
white sponge nevus of cannon [NCBI] 0.000481453
behcet syndrome [NCBI] 0.000317551
klippel-trenaunay-weber syndrome [NCBI] 0.000257155
LSA [NCBI] 0.000235782
OCP [NCBI] 0.000158093
focal epithelial hyperplasia of the oral mucosa [NCBI] 0.000120229
cranioacrofacial syndrome [NCBI] 0.000120229
ermine phenotype [NCBI] 9.77659e-05
limb deficiencies, distal, with micrognathia [NCBI] 9.77659e-05
DSG3 [NCBI] 9.21613e-05
keratin 6, hair follicle [NCBI] 9.02832e-05
abcd syndrome [NCBI] 8.92934e-05
pachyonychia congenita, recessive [NCBI] 8.92934e-05
KRT6B [NCBI] 7.65036e-05
KRT4 [NCBI] 7.13032e-05
KRT6A [NCBI] 6.79265e-05
TS [NCBI] 6.63112e-05
de sanctis-cacchione syndrome [NCBI] 6.60038e-05
CHD7 [NCBI] 6.34153e-05
stuve-wiedemann syndrome [NCBI] 6.08072e-05
PJS [NCBI] 5.8163e-05
SCN1 [NCBI] 5.60514e-05
KLK7 [NCBI] 5.52508e-05
PPS [NCBI] 5.23988e-05
ECM1 [NCBI] 5.13588e-05
HLA-DQB1 [NCBI] 4.98678e-05
EBR1 [NCBI] 4.94362e-05
SLE [NCBI] 4.84214e-05
apnea, obstructive sleep [NCBI] 4.79655e-05
DA2A [NCBI] 4.69462e-05
charge syndrome [NCBI] 4.56234e-05
DKC [NCBI] 4.48004e-05
DSG1 [NCBI] 4.46225e-05
RA [NCBI] 4.3815e-05
APCS [NCBI] 4.35931e-05
XPA [NCBI] 4.29165e-05
mucopolysaccharidosis type iva [NCBI] 4.10264e-05
ESR1 [NCBI] 3.82565e-05
SLS [NCBI] 3.3655e-05
EV [NCBI] 2.38978e-05
PCNA [NCBI] 2.12135e-05
PTHLH [NCBI] 1.90292e-05
MUC1 [NCBI] 1.53883e-05
FA [NCBI] 6.54834e-06
CD [NCBI] 4.99947e-06
CEACAM5 [NCBI] 2.2617e-06
EGF [NCBI] 1.99224e-06
thrombocytopenic purpura, autoimmune [NCBI] 6.93304e-07



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