Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Corneal Diseases [NCBI]


Gene


Gene Link Information
Gain
01
MGC1 [NCBI] 0.000438875
MACOM [NCBI] 0.000438875
KERA [NCBI] 0.00012989
PAX6 [NCBI] 9.81679e-05
TGFBI [NCBI] 8.14381e-05
KRT3 [NCBI] 5.89677e-05
EGF [NCBI] 3.83071e-05
LUM [NCBI] 2.0757e-05
PITX2 [NCBI] 1.72612e-05
OCRL [NCBI] 1.58098e-05
ZNF469 [NCBI] 1.52992e-05
DEFB1 [NCBI] 1.39061e-05
EPYC [NCBI] 1.29189e-05
LCAT [NCBI] 1.27694e-05
DEFB4 [NCBI] 1.24544e-05
ITGA8 [NCBI] 1.10038e-05
TJP1 [NCBI] 1.03945e-05
CKAP4 [NCBI] 1.02599e-05
MMP24 [NCBI] 9.91002e-06
MPV17 [NCBI] 9.71906e-06
TKT [NCBI] 9.71906e-06
OGN [NCBI] 9.54729e-06
ABCG2 [NCBI] 9.4271e-06
LAMB3 [NCBI] 9.11647e-06
KRT12 [NCBI] 9.11617e-06
SLC4A11 [NCBI] 8.87931e-06
ITGB6 [NCBI] 8.77215e-06
HGD [NCBI] 8.77215e-06
NHS [NCBI] 8.67131e-06
ALDH3A1 [NCBI] 8.48591e-06
AQP3 [NCBI] 8.02656e-06
LAMA5 [NCBI] 8.02656e-06
MSRA [NCBI] 7.89735e-06
ATN1 [NCBI] 7.77725e-06
MCOLN1 [NCBI] 7.1939e-06
DCN [NCBI] 7.15324e-06
TAC1 [NCBI] 7.11354e-06
NGF [NCBI] 7.08638e-06
KRT1 [NCBI] 6.9634e-06
POSTN [NCBI] 6.79269e-06
LTF [NCBI] 6.76051e-06
COCH [NCBI] 6.69795e-06
TNC [NCBI] 6.55098e-06
FOXC1 [NCBI] 6.24304e-06
VIP [NCBI] 6.22634e-06
ZBTB16 [NCBI] 6.04417e-06
AQP4 [NCBI] 5.74007e-06
MUC4 [NCBI] 5.62262e-06
NID1 [NCBI] 5.52814e-06
ITGA2B [NCBI] 5.48283e-06
MAPK8 [NCBI] 5.36772e-06
FBN1 [NCBI] 5.35388e-06
HLA-G [NCBI] 5.19617e-06
ABCA1 [NCBI] 4.99572e-06
ITGB1 [NCBI] 4.83707e-06
ATXN1 [NCBI] 4.62904e-06
TGFB2 [NCBI] 4.54259e-06
CDK5 [NCBI] 4.51753e-06
BMP4 [NCBI] 4.32247e-06
FLT1 [NCBI] 4.05245e-06
CLU [NCBI] 3.7844e-06
PROM1 [NCBI] 3.68775e-06
SHH [NCBI] 3.68775e-06
HLA-A [NCBI] 3.49755e-06
CCL11 [NCBI] 3.30488e-06
CCR5 [NCBI] 3.2706e-06
TP63 [NCBI] 3.26308e-06
MMP2 [NCBI] 3.21875e-06
CCR2 [NCBI] 3.17922e-06
PCNA [NCBI] 3.04598e-06
MMP9 [NCBI] 2.85798e-06
BMP2 [NCBI] 2.84942e-06
TLR2 [NCBI] 2.83246e-06
CTGF [NCBI] 2.70857e-06
ADA [NCBI] 2.24389e-06
SOD1 [NCBI] 1.78634e-06
TH [NCBI] 1.62417e-06
IL6 [NCBI] 1.57174e-06
NOS3 [NCBI] 1.46548e-06
CD68 [NCBI] 1.45953e-06
NOS2 [NCBI] 1.29184e-06
HGF [NCBI] 1.23967e-06
CTNNB1 [NCBI] 1.05294e-06
TGFB1 [NCBI] 9.53402e-07
FASLG [NCBI] 8.42974e-07
VEGFA [NCBI] 7.41793e-07
TNF [NCBI] 1.34701e-08




OMIM


OMIM Link Information
gain
01
MACOM [NCBI] 0.00279952
ehlers-danlos syndrome, type vib [NCBI] 0.00126979
alacrima, congenital [NCBI] 0.0010375
MGC1 [NCBI] 0.0010375
cornea guttata with anterior polar cataracts [NCBI] 0.0010375
CND [NCBI] 0.000737684
CNA1 [NCBI] 0.000684465
OCP [NCBI] 0.000451295
KERA [NCBI] 0.000376382
CNA2 [NCBI] 0.000285744
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000271087
corneal dystrophy, gelatinous drop-like [NCBI] 0.000243839
corneal degeneration, band-shaped spheroid [NCBI] 0.000204216
keratitis, hereditary [NCBI] 0.000180644
ATS [NCBI] 0.000177193
EGF [NCBI] 0.000144483
KTCN1 [NCBI] 0.000128314
FED [NCBI] 0.000123813
VRNI [NCBI] 0.000118779
corneodermatoosseous syndrome [NCBI] 0.000117451
corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation [NCBI] 0.000117451
mucolipidosis iv [NCBI] 0.000114221
AN2 [NCBI] 9.89341e-05
RDC [NCBI] 9.49899e-05
SLE [NCBI] 8.17179e-05
LOCS [NCBI] 8.10223e-05
DSPG3 [NCBI] 8.01986e-05
corneal dystrophy and perceptive deafness [NCBI] 7.69378e-05
PAX6 [NCBI] 7.39628e-05
foveal hypoplasia and presenile cataract syndrome [NCBI] 7.09823e-05
NN [NCBI] 7.09823e-05
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation [NCBI] 7.09823e-05
corneal dystrophy, epithelial basement membrane [NCBI] 6.867e-05
ASMD [NCBI] 6.48565e-05
RA [NCBI] 6.31403e-05
wagr syndrome [NCBI] 6.17799e-05
alport syndrome, autosomal recessive [NCBI] 6.17799e-05
LADD [NCBI] 6.0439e-05
CDL1 [NCBI] 6.0439e-05
morquio syndrome b [NCBI] 5.92022e-05
plasminogen deficiency, type i [NCBI] 5.92022e-05
KRT3 [NCBI] 5.78478e-05
OGN [NCBI] 5.78478e-05
NCIE1 [NCBI] 5.69848e-05
KRT12 [NCBI] 5.33406e-05
MPV17 [NCBI] 5.33406e-05
CIPA [NCBI] 5.33081e-05
NHS [NCBI] 5.33081e-05
PALS [NCBI] 5.25088e-05
lymphedema-distichiasis syndrome [NCBI] 5.1748e-05
TKT [NCBI] 5.16791e-05
ehlers-danlos syndrome, type vi [NCBI] 4.96647e-05
LCAT [NCBI] 4.69253e-05
MCOPS7 [NCBI] 4.51755e-05
PFIC1 [NCBI] 4.42303e-05
MCOLN1 [NCBI] 4.372e-05
FOXC1 [NCBI] 4.18593e-05
tyrosine transaminase deficiency [NCBI] 4.18593e-05
DCN [NCBI] 4.13098e-05
CMTC [NCBI] 3.98701e-05
LI1 [NCBI] 3.82373e-05
PITX2 [NCBI] 3.81408e-05
CTNS [NCBI] 3.73362e-05
RTS [NCBI] 3.67642e-05
ZNF145 [NCBI] 3.63762e-05
ABCA1 [NCBI] 3.63762e-05
ALGS1 [NCBI] 3.32785e-05
SMS [NCBI] 2.69261e-05
ichthyosis, x-linked [NCBI] 2.65277e-05
GUSB [NCBI] 2.56429e-05
fabry disease [NCBI] 2.51918e-05
FBN1 [NCBI] 2.40013e-05
DRPLA [NCBI] 2.1399e-05
PLG [NCBI] 2.12641e-05
VIP [NCBI] 2.1089e-05
NGFB [NCBI] 2.0221e-05
MFS [NCBI] 1.45227e-05
CTGF [NCBI] 1.30165e-05
ADA [NCBI] 6.17334e-06
PCNA [NCBI] 5.92666e-06
TNF [NCBI] 4.06932e-06
RP [NCBI] 3.33752e-06
TH [NCBI] 3.09548e-06
HGF [NCBI] 2.1144e-06
VEGF [NCBI] 4.27613e-07
CJD [NCBI] 4.03014e-07
CEACAM5 [NCBI] 3.5225e-07




Database Center for Life Science