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MeSH keywords -> Related genes, diseases (OMIM)


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01 Corneal Opacity [NCBI]


Gene


Gene Link Information
Gain
01
CDB2 [NCBI] 0.000438875
LCAT [NCBI] 0.000122364
TGFBI [NCBI] 0.000122249
PAX6 [NCBI] 6.18896e-05
FOXE3 [NCBI] 2.55902e-05
KERA [NCBI] 2.26131e-05
FOXC1 [NCBI] 1.80411e-05
LUM [NCBI] 1.0684e-05
TBCE [NCBI] 1.01433e-05
CRYAA [NCBI] 9.59277e-06
MSRA [NCBI] 9.46327e-06
DCN [NCBI] 8.71708e-06
GALNS [NCBI] 8.25999e-06
GLA [NCBI] 7.97642e-06
CSTB [NCBI] 7.17784e-06
TAT [NCBI] 6.63683e-06
APOA1 [NCBI] 6.09333e-06
HP [NCBI] 5.06569e-06
CETP [NCBI] 3.71112e-06
TGFB1 [NCBI] 2.23598e-06
EGF [NCBI] 1.17117e-06




OMIM


OMIM Link Information
gain
01
corneal dystrophy, crystalline, of schnyder [NCBI] 0.00272372
cutis laxa, corneal clouding, and mental retardation [NCBI] 0.0013128
spondyloepiphyseal dysplasia tarda, toledo type [NCBI] 0.0013128
FED [NCBI] 0.00121967
LCAT [NCBI] 0.00105704
acromegaloid changes, cutis verticis gyrata, and corneal leukoma [NCBI] 0.000952205
CND [NCBI] 0.000652698
persistent hyperplastic primary vitreous, autosomal recessive [NCBI] 0.000599634
CNA1 [NCBI] 0.000599634
dermochondrocorneal dystrophy [NCBI] 0.000560268
mucolipidosis iv [NCBI] 0.000524531
RNANC [NCBI] 0.000503004
CHED1 [NCBI] 0.000503004
CDB2 [NCBI] 0.000461483
MCOP1 [NCBI] 0.000444338
MCOPS1 [NCBI] 0.00042895
osteolysis, hereditary, of carpal bones with nephropathy [NCBI] 0.000390496
microcephalic osteodysplastic primordial dwarfism, type i [NCBI] 0.000360016
CSCD [NCBI] 0.00030377
FRNS [NCBI] 0.000273342
peters anomaly [NCBI] 0.000272844
lecithin:cholesterol acyltransferase deficiency [NCBI] 0.000268221
mucopolysaccharidoses, unclassified types [NCBI] 0.000195673
ichthyosis, x-linked [NCBI] 0.000165304
WARBM [NCBI] 0.000153775
winchester syndrome [NCBI] 0.000149435
CDB1 [NCBI] 0.000139114
CDGG1 [NCBI] 0.000129097
SLE [NCBI] 0.000116966
brachymesomelia-renal syndrome [NCBI] 0.000113208
kyrle disease [NCBI] 0.000113208
peters anomaly with cataract [NCBI] 0.000113208
sclerocornea [NCBI] 0.000113208
congenital corneal opacities, cornea guttata, and corectopia [NCBI] 0.000113208
MCOPS7 [NCBI] 0.000104764
mucopolysaccharidosis type vi [NCBI] 0.000103781
TGD [NCBI] 0.000102827
tyrosine transaminase deficiency [NCBI] 9.96173e-05
DCN [NCBI] 9.84825e-05
subaortic stenosis--short stature syndrome [NCBI] 9.075e-05
mental retardation syndrome, mietens-weber type [NCBI] 9.075e-05
coloboma, uveal, with cleft lip and palate and mental retardation [NCBI] 8.22828e-05
corneal degeneration, band-shaped spheroid [NCBI] 8.22828e-05
moved to 310600 [NCBI] 8.22828e-05
hurler syndrome [NCBI] 8.22721e-05
OCP [NCBI] 7.82004e-05
APOA1 [NCBI] 7.78607e-05
PAX6 [NCBI] 7.5323e-05
corneal fleck dystrophy [NCBI] 7.27084e-05
CNA2 [NCBI] 6.94592e-05
GBA [NCBI] 6.77995e-05
short syndrome [NCBI] 6.4451e-05
gaucher disease, type iiic [NCBI] 6.4451e-05
hypoalphalipoproteinemia, primary [NCBI] 6.4451e-05
bietti crystalline corneoretinal dystrophy [NCBI] 6.4451e-05
cataract-microcornea syndrome [NCBI] 6.4451e-05
corneal dystrophy, epithelial basement membrane [NCBI] 6.4451e-05
fabry disease [NCBI] 6.37216e-05
PIP5K3 [NCBI] 6.19002e-05
ASMD [NCBI] 6.06443e-05
HRD [NCBI] 5.90355e-05
KCS [NCBI] 5.90355e-05
SLC4A4 [NCBI] 5.85252e-05
corneal dystrophy, gelatinous drop-like [NCBI] 5.75747e-05
wagr syndrome [NCBI] 5.75747e-05
CDA [NCBI] 5.50039e-05
MCDC1 [NCBI] 5.17945e-05
CIPA [NCBI] 4.91306e-05
MAN2B1 [NCBI] 4.6692e-05
FOXC1 [NCBI] 4.25339e-05
gm1-gangliosidosis, type i [NCBI] 4.1043e-05
TGFBI [NCBI] 3.962e-05
mannosidosis, alpha b, lysosomal [NCBI] 3.92211e-05
CSTB [NCBI] 3.77166e-05
walker-warburg syndrome [NCBI] 3.75951e-05
FDH [NCBI] 3.6128e-05
AN2 [NCBI] 3.41672e-05
CSA [NCBI] 3.35675e-05
myoclonic epilepsy of unverricht and lundborg [NCBI] 3.32765e-05
HP [NCBI] 1.47003e-05
VRNI [NCBI] 5.97617e-06
TNFSF6 [NCBI] 5.83454e-06
EGF [NCBI] 3.07512e-07




Database Center for Life Science