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01 Myopia [NCBI]


Gene


Gene Link Information
Gain
01
MYP2 [NCBI] 0.00120734
OPEM [NCBI] 0.000653599
MYP12 [NCBI] 0.000653599
MYP3 [NCBI] 0.000569949
MYP13 [NCBI] 0.000325647
MYP10 [NCBI] 0.000325647
COD2 [NCBI] 0.000325647
MYP4 [NCBI] 0.000325647
MYP6 [NCBI] 0.000325647
MACOM [NCBI] 0.000325647
MYP5 [NCBI] 0.000325647
MYP1 [NCBI] 0.000325647
MYP8 [NCBI] 0.000325647
MYP7 [NCBI] 0.000325647
MYP9 [NCBI] 0.000325647
OED [NCBI] 0.000264926
CNA1 [NCBI] 0.000264926
COL2A1 [NCBI] 9.40933e-05
TGIF1 [NCBI] 6.63808e-05
PAX6 [NCBI] 6.29176e-05
NYX [NCBI] 4.43802e-05
TGFBI [NCBI] 2.76898e-05
COL18A1 [NCBI] 2.70073e-05
TGFB1 [NCBI] 2.44262e-05
MYOC [NCBI] 1.88293e-05
SOX2 [NCBI] 1.59514e-05
OPA1 [NCBI] 1.47214e-05
EPYC [NCBI] 1.33268e-05
VIP [NCBI] 1.25326e-05
ZFP161 [NCBI] 1.24285e-05
POLS [NCBI] 1.18452e-05
CLUL1 [NCBI] 1.18452e-05
COL1A1 [NCBI] 1.18344e-05
IRX2 [NCBI] 1.10659e-05
IRX1 [NCBI] 1.10659e-05
DGKD [NCBI] 1.07786e-05
PMM1 [NCBI] 1.07786e-05
CHRM5 [NCBI] 1.07786e-05
OPTC [NCBI] 1.07786e-05
BFSP2 [NCBI] 1.05326e-05
VPS13B [NCBI] 1.05326e-05
CCT5 [NCBI] 1.03176e-05
EGR1 [NCBI] 1.02015e-05
GJA8 [NCBI] 1.01266e-05
CTNND2 [NCBI] 1.01266e-05
COL9A1 [NCBI] 1.01266e-05
LPIN2 [NCBI] 9.95474e-06
COL11A1 [NCBI] 9.52348e-06
MFRP [NCBI] 9.52348e-06
LUM [NCBI] 9.52348e-06
TULP1 [NCBI] 8.98316e-06
KERA [NCBI] 8.89292e-06
VIPR2 [NCBI] 8.89292e-06
NIPBL [NCBI] 8.80721e-06
CHRM1 [NCBI] 8.72559e-06
NR2E3 [NCBI] 8.3674e-06
CACNA1F [NCBI] 7.9158e-06
SIX3 [NCBI] 7.9158e-06
PITX2 [NCBI] 7.81939e-06
DCN [NCBI] 7.55912e-06
RP2 [NCBI] 7.48052e-06
PDE6B [NCBI] 7.36903e-06
LAMP2 [NCBI] 7.29857e-06
OAT [NCBI] 7.13424e-06
ZEB2 [NCBI] 7.13424e-06
ALDH3A2 [NCBI] 6.98442e-06
CHM [NCBI] 6.71947e-06
OPTN [NCBI] 6.69512e-06
TIMP3 [NCBI] 5.94611e-06
RPGR [NCBI] 5.87035e-06
TSC2 [NCBI] 5.49978e-06
TIMP1 [NCBI] 5.38514e-06
EGF [NCBI] 5.32045e-06
FGF2 [NCBI] 5.24703e-06
CYP1B1 [NCBI] 4.85021e-06
MMP3 [NCBI] 4.80281e-06
DAG1 [NCBI] 4.57766e-06
SERPINF1 [NCBI] 4.35604e-06
ALDH2 [NCBI] 4.17698e-06
PRKCB [NCBI] 3.88719e-06
LAMB3 [NCBI] 3.79292e-06
CHAT [NCBI] 3.0197e-06
BDNF [NCBI] 2.03535e-06
FASLG [NCBI] 1.13994e-06
NGF [NCBI] 1.11316e-06




OMIM


OMIM Link Information
gain
01
MYP2 [NCBI] 0.00903571
MYP1 [NCBI] 0.00215012
OPEM [NCBI] 0.00166522
knobloch syndrome, type ii [NCBI] 0.00166522
myopia 6 [NCBI] 0.00136577
MYP3 [NCBI] 0.00123085
ectopia lentis with ectopia of pupil [NCBI] 0.00123085
MACOM [NCBI] 0.00123085
STL1 [NCBI] 0.000841793
myopia 12 [NCBI] 0.000830911
CORDX2 [NCBI] 0.000830911
microcoria, congenital [NCBI] 0.000830911
myopia 13 [NCBI] 0.000830911
myopia 5 [NCBI] 0.000613741
myopia 8 [NCBI] 0.000613741
myopia 10 [NCBI] 0.000613741
myopia 9 [NCBI] 0.000613741
myopia 14 [NCBI] 0.000613741
CACD [NCBI] 0.000613741
myopia 7 [NCBI] 0.000613741
myopia 4 [NCBI] 0.000613741
vitreoretinal degeneration, snowflake type [NCBI] 0.000532264
chorioretinal atrophy, progressive bifocal [NCBI] 0.00047963
ophthalmoplegia, familial static [NCBI] 0.00047963
KNO [NCBI] 0.000438584
alport syndrome, autosomal dominant [NCBI] 0.000418599
CTPP1 [NCBI] 0.000409827
AIED [NCBI] 0.000368808
oculocerebral syndrome with hypopigmentation [NCBI] 0.000362544
CSNB1A [NCBI] 0.0003521
kenny-caffey syndrome, type 2 [NCBI] 0.000311958
WZS [NCBI] 0.000310444
marshall syndrome [NCBI] 0.000294722
CBBM [NCBI] 0.000274795
lymphedema, microcephaly, chorioretinopathy syndrome [NCBI] 0.000254649
donnai-barrow syndrome [NCBI] 0.000252606
COL2A1 [NCBI] 0.000223035
deafness, cochlear, with myopia and intellectual impairment [NCBI] 0.000219856
fundus dystrophy, pseudoinflammatory, recessive form [NCBI] 0.000188919
MEB [NCBI] 0.000160523
COH1 [NCBI] 0.000154367
SLE [NCBI] 0.000153107
CSNB1B [NCBI] 0.000152059
cataract-microcornea syndrome [NCBI] 0.000147039
SFD [NCBI] 0.000124611
WGN1 [NCBI] 0.000124611
papillorenal syndrome [NCBI] 0.000118362
microspherophakia with hernia [NCBI] 0.000109848
spondyloepiphyseal dysplasia, myopia, and sensorineural deafness [NCBI] 0.000109848
dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy [NCBI] 0.000109848
gastrocutaneous syndrome [NCBI] 0.000109848
blepharoptosis, myopia, and ectopia lentis [NCBI] 0.000109848
epiphyseal dysplasia of femoral head, myopia, and deafness [NCBI] 0.000109848
lattice degeneration of retina leading to retinal detachment [NCBI] 0.000109848
polydactyly, postaxial, with progressive myopia [NCBI] 0.000109848
sinus node disease and myopia [NCBI] 0.000109848
myopia, infantile severe [NCBI] 0.000109848
COL18A1 [NCBI] 0.000108271
COL11A1 [NCBI] 0.000104948
LRP2 [NCBI] 0.000102103
SEDC [NCBI] 9.43677e-05
GLC1A [NCBI] 9.34974e-05
spinocerebellar degeneration with macular corneal dystrophy, congenital cataracts, and myopia [NCBI] 8.73936e-05
growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction [NCBI] 8.73936e-05
epiphyseal dysplasia, multiple, with myopia and conductive deafness [NCBI] 8.73936e-05
camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye [NCBI] 8.73936e-05
limb deficiencies, distal, with micrognathia [NCBI] 8.73936e-05
CHM [NCBI] 8.21358e-05
oculocerebral hypopigmentation syndrome of preus [NCBI] 7.89299e-05
cataract, autosomal dominant, multiple types 1 [NCBI] 7.34399e-05
CORD6 [NCBI] 7.34399e-05
VIPR2 [NCBI] 6.70987e-05
chorioretinal dysplasia-microcephaly-mental retardation syndrome [NCBI] 6.61167e-05
SCRA [NCBI] 6.61167e-05
MYOC [NCBI] 6.56162e-05
RCD3A [NCBI] 6.34207e-05
STL2 [NCBI] 6.34207e-05
SMS [NCBI] 6.09176e-05
COH1 [NCBI] 5.85252e-05
weill-marchesani syndrome, autosomal recessive [NCBI] 5.73156e-05
NYX [NCBI] 5.60164e-05
IRID1 [NCBI] 5.57103e-05
WSS [NCBI] 5.4253e-05
COL9A1 [NCBI] 5.40176e-05
TGIF [NCBI] 5.2356e-05
CORDX1 [NCBI] 5.16891e-05
LPIN2 [NCBI] 5.09339e-05
kniest dysplasia [NCBI] 5.05486e-05
BFSP2 [NCBI] 4.96909e-05
POMGNT1 [NCBI] 4.96909e-05
CORD2 [NCBI] 4.75544e-05
DHRD [NCBI] 4.75544e-05
immunoosseous dysplasia, schimke type [NCBI] 4.66718e-05
CACNA1F [NCBI] 4.58656e-05
danon disease [NCBI] 4.58366e-05
KTCN1 [NCBI] 4.50442e-05
VIP [NCBI] 4.44627e-05
ehlers-danlos syndrome, type vi [NCBI] 4.22278e-05
SLC6A3 [NCBI] 4.21038e-05
GJA8 [NCBI] 4.19842e-05
GUCY2D [NCBI] 4.19842e-05
OPA1 [NCBI] 4.04986e-05
biotinidase deficiency [NCBI] 4.04103e-05
TIMP3 [NCBI] 3.962e-05
EGR1 [NCBI] 3.84342e-05
NRCLP1 [NCBI] 3.73212e-05
OPTN [NCBI] 3.58345e-05
POAG [NCBI] 3.55662e-05
ehlers-danlos syndrome, type i [NCBI] 3.55662e-05
contractural arachnodactyly, congenital [NCBI] 3.528e-05
TGFB1 [NCBI] 3.15277e-05
PAX6 [NCBI] 3.06539e-05
RP [NCBI] 2.99567e-05
TNC [NCBI] 2.60931e-05
RHO [NCBI] 2.56882e-05
homocystinuria [NCBI] 2.47463e-05
SLS [NCBI] 2.39743e-05
VRNI [NCBI] 1.93588e-05
CDLS1 [NCBI] 1.86457e-05
FGF7 [NCBI] 1.78047e-05
EGF [NCBI] 8.86234e-06
MFS [NCBI] 8.66093e-06
CHAT [NCBI] 8.65674e-06
GTS [NCBI] 3.69872e-06
NGFB [NCBI] 6.60907e-07
PWS [NCBI] 4.58286e-07




Database Center for Life Science