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MeSH keywords -> Related genes, diseases (OMIM)


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01 Airway Obstruction [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.00174825
DNASE1 [NCBI] 2.30942e-05
TNF [NCBI] 2.16773e-05
ADAM33 [NCBI] 1.76345e-05
MPO [NCBI] 1.68368e-05
FCHSD2 [NCBI] 1.67592e-05
SLC4A10 [NCBI] 1.43788e-05
MED27 [NCBI] 1.34804e-05
GNAI3 [NCBI] 1.21176e-05
VEGFA [NCBI] 1.08977e-05
ARSE [NCBI] 1.03374e-05
GNAI2 [NCBI] 9.29255e-06
TLR4 [NCBI] 8.55817e-06
DLX3 [NCBI] 8.27873e-06
S100A12 [NCBI] 8.2135e-06
TLR7 [NCBI] 7.39169e-06
MARCKS [NCBI] 7.29568e-06
SERPING1 [NCBI] 7.03648e-06
NFKBIB [NCBI] 7.02053e-06
FGFR2 [NCBI] 6.02843e-06
CYSLTR1 [NCBI] 5.99351e-06
CD14 [NCBI] 5.80569e-06
BPI [NCBI] 5.79031e-06
FGF7 [NCBI] 5.745e-06
MET [NCBI] 5.73757e-06
MMP1 [NCBI] 5.56842e-06
CCL5 [NCBI] 5.54843e-06
CCR7 [NCBI] 5.53524e-06
IGFBP3 [NCBI] 5.43949e-06
SCGB1A1 [NCBI] 5.37858e-06
LBP [NCBI] 5.37261e-06
CFTR [NCBI] 5.1925e-06
NKX2-1 [NCBI] 4.96291e-06
CCL11 [NCBI] 4.7091e-06
FGFR3 [NCBI] 4.45837e-06
ADA [NCBI] 3.59452e-06
VIP [NCBI] 3.359e-06
TG [NCBI] 3.16683e-06
NOS2 [NCBI] 2.54055e-06
HGF [NCBI] 2.47999e-06
PCNA [NCBI] 1.74077e-06
EGFR [NCBI] 1.18535e-06



OMIM


 OMIM Link Information
gain		 01
apnea, obstructive sleep [NCBI] 0.018084
mucus inspissation of respiratory tract [NCBI] 0.000567522
CF [NCBI] 0.000513305
laryngeal abductor paralysis [NCBI] 0.000395303
spondyloepimetaphyseal dysplasia with multiple dislocations [NCBI] 0.000282904
RNASE3 [NCBI] 0.00026289
hurler syndrome [NCBI] 0.000150914
hurler-scheie syndrome [NCBI] 0.000132114
MAFD6 [NCBI] 0.000126053
tracheopathia osteoplastica [NCBI] 0.000115756
AMC [NCBI] 8.58369e-05
HAE III [NCBI] 7.52477e-05
marshall-smith syndrome [NCBI] 6.92947e-05
MEF2C [NCBI] 6.91714e-05
fabry disease [NCBI] 6.85956e-05
phace association [NCBI] 6.69838e-05
plasminogen deficiency, type i [NCBI] 5.75236e-05
marshall syndrome [NCBI] 5.53087e-05
SMMCI [NCBI] 5.2478e-05
CPI [NCBI] 5.22243e-05
TNF [NCBI] 5.19442e-05
weaver syndrome [NCBI] 4.8663e-05
HSS [NCBI] 4.8663e-05
TLR7 [NCBI] 4.71691e-05
MPO [NCBI] 4.67047e-05
CHNG2 [NCBI] 4.45253e-05
SLE [NCBI] 4.28012e-05
charge syndrome [NCBI] 4.1265e-05
kartagener syndrome [NCBI] 3.66059e-05
CSA [NCBI] 3.60018e-05
RTS [NCBI] 3.51392e-05
TSC2 [NCBI] 3.10082e-05
mucopolysaccharidosis type ii [NCBI] 2.70353e-05
AGER [NCBI] 2.48872e-05
PLG [NCBI] 2.39068e-05
CD [NCBI] 2.38976e-05
ACH [NCBI] 2.34014e-05
PCD [NCBI] 1.84963e-05
LAM [NCBI] 1.71642e-05
TLR4 [NCBI] 1.545e-05
PTHLH [NCBI] 1.23184e-05
HD [NCBI] 1.00815e-05
AT [NCBI] 9.76737e-06
RA [NCBI] 9.53508e-06
ADA [NCBI] 8.31167e-06
polycystic kidneys [NCBI] 7.99875e-06
NPPA [NCBI] 7.72505e-06
VIP [NCBI] 7.07385e-06
TG [NCBI] 6.3344e-06
MG [NCBI] 3.26758e-06
PWS [NCBI] 2.50237e-06
VEGF [NCBI] 2.44427e-06
PCNA [NCBI] 9.0011e-07
EGFR [NCBI] 2.08268e-07
CJD [NCBI] 1.25317e-07
CEACAM5 [NCBI] 2.36782e-09



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