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MeSH keywords -> Related genes, diseases (OMIM)


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01 Fibroma [NCBI]

Gene


 Gene Link Information
Gain		 01
CD99 [NCBI] 0.00020348
ANTXR2 [NCBI] 4.61567e-05
FLCN [NCBI] 3.83385e-05
CD68 [NCBI] 3.48638e-05
CD34 [NCBI] 2.71961e-05
CTNNB1 [NCBI] 2.52156e-05
CREB3L2 [NCBI] 2.48763e-05
APC [NCBI] 1.85171e-05
ALK [NCBI] 1.7134e-05
YJEFN3 [NCBI] 1.57072e-05
ACVRL1 [NCBI] 1.41948e-05
APOA1BP [NCBI] 1.33268e-05
EDC3 [NCBI] 1.24285e-05
PROM2 [NCBI] 1.24285e-05
GNAS [NCBI] 1.21025e-05
CREB3L1 [NCBI] 1.14115e-05
TGFBR1 [NCBI] 1.00741e-05
MUCL1 [NCBI] 9.7986e-06
FUS [NCBI] 8.80721e-06
AKT3 [NCBI] 8.1267e-06
AGA [NCBI] 7.55912e-06
ST14 [NCBI] 7.48052e-06
S100A2 [NCBI] 7.36903e-06
NOV [NCBI] 7.16586e-06
PTCH1 [NCBI] 6.76924e-06
PDGFB [NCBI] 6.74417e-06
MME [NCBI] 6.57837e-06
CDC73 [NCBI] 6.53383e-06
INHBA [NCBI] 6.44814e-06
CD177 [NCBI] 6.36659e-06
GLI1 [NCBI] 6.30792e-06
DEFB1 [NCBI] 6.16077e-06
AKT2 [NCBI] 6.00929e-06
ABCC6 [NCBI] 5.96169e-06
VIM [NCBI] 5.71483e-06
DEFB4 [NCBI] 5.44147e-06
CNN1 [NCBI] 5.41871e-06
VCAN [NCBI] 5.38514e-06
PMS2 [NCBI] 5.22676e-06
WT1 [NCBI] 5.19683e-06
SAT2 [NCBI] 5.05476e-06
STK11 [NCBI] 4.81061e-06
APOD [NCBI] 4.64695e-06
TGFB1 [NCBI] 4.5405e-06
NOTCH1 [NCBI] 4.36792e-06
AR [NCBI] 4.35823e-06
CKAP4 [NCBI] 4.35604e-06
CXCL1 [NCBI] 4.28654e-06
ETV6 [NCBI] 4.28088e-06
PDGFA [NCBI] 4.20907e-06
SHH [NCBI] 4.0794e-06
MEN1 [NCBI] 3.78876e-06
PCNA [NCBI] 3.73344e-06
TFF1 [NCBI] 3.52232e-06
MYC [NCBI] 3.40122e-06
CTGF [NCBI] 3.08658e-06
CCL2 [NCBI] 2.77662e-06
EGF [NCBI] 2.40113e-06
TG [NCBI] 2.20455e-06
PTEN [NCBI] 1.7327e-06
AKT1 [NCBI] 1.53855e-06
GFAP [NCBI] 1.17941e-06
TP53 [NCBI] 1.02462e-06
TNF [NCBI] 1.09109e-08



OMIM


 OMIM Link Information
gain		 01
CGF [NCBI] 0.0132541
terminal osseous dysplasia and pigmentary defects [NCBI] 0.00260082
fibromatosis, juvenile hyaline [NCBI] 0.00130509
APC [NCBI] 0.00104218
stiff skin syndrome [NCBI] 0.000467507
dupuytren contracture [NCBI] 0.000467507
pachydermodactyly, familial [NCBI] 0.0004509
ZLS [NCBI] 0.000438064
DFSP [NCBI] 0.000403122
BHD [NCBI] 0.000278919
hyalinosis, infantile systemic [NCBI] 0.000270516
desmoid disease, hereditary [NCBI] 0.000245115
trichodiscomas, familial multiple [NCBI] 0.000225069
MUC1 [NCBI] 0.000224216
HRPT2 [NCBI] 0.000203794
buschke-ollendorff syndrome [NCBI] 0.000201101
ANTXR2 [NCBI] 0.000145
TS [NCBI] 0.000113182
polyps, multiple and recurrent inflammatory fibroid, gastrointestinal [NCBI] 0.00011244
ovarian fibromata [NCBI] 0.00011244
apc gene [NCBI] 0.000100348
AACT [NCBI] 9.74082e-05
noduli cutanei, multiple, with urinary tract abnormalities [NCBI] 8.99832e-05
keloids [NCBI] 8.15167e-05
IGFALS [NCBI] 7.12069e-05
ramon syndrome [NCBI] 6.86954e-05
aplasia cutis congenita with epibulbar dermoids [NCBI] 6.86954e-05
GIST [NCBI] 6.78028e-05
CD [NCBI] 6.2786e-05
winchester syndrome [NCBI] 6.16726e-05
GINGF [NCBI] 5.54784e-05
ALK [NCBI] 5.19182e-05
BCNS [NCBI] 5.12319e-05
mucolipidosis iiia [NCBI] 4.68252e-05
lipoid proteinosis of urbach and wiethe [NCBI] 4.47545e-05
farber lipogranulomatosis [NCBI] 4.47134e-05
HRPT1 [NCBI] 4.12972e-05
COL6A1 [NCBI] 4.05964e-05
MCOPS7 [NCBI] 4.02988e-05
aspartylglucosaminuria [NCBI] 3.80225e-05
CMTC [NCBI] 3.50479e-05
TSC1 [NCBI] 3.47554e-05
mucolipidosis ii [NCBI] 3.19841e-05
TSC2 [NCBI] 2.99365e-05
VIM [NCBI] 2.87494e-05
NPM1 [NCBI] 2.71545e-05
FOP [NCBI] 2.69164e-05
SPINK1 [NCBI] 2.2155e-05
krabbe disease [NCBI] 2.02006e-05
PI [NCBI] 1.71238e-05
NF1 [NCBI] 1.52549e-05
CEACAM5 [NCBI] 1.16887e-05
PCNA [NCBI] 8.01341e-06
TG [NCBI] 5.53154e-06
EGF [NCBI] 2.66418e-06
TNF [NCBI] 2.37119e-06
AR [NCBI] 2.13719e-06
GFAP [NCBI] 1.23657e-06
VEGF [NCBI] 9.85562e-09



Database Center for Life Science