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01 Blindness [NCBI]

Gene


 Gene Link Information
Gain		 01
RPE65 [NCBI] 0.000580898
NDP [NCBI] 0.000372976
SLSN3 [NCBI] 0.000357173
CND [NCBI] 0.000357173
PRD [NCBI] 0.000357173
TIMM8AP [NCBI] 0.000357173
GUCY2D [NCBI] 0.000306351
CTD [NCBI] 0.000296439
CACD [NCBI] 0.000210456
CRB1 [NCBI] 0.000203944
AIPL1 [NCBI] 0.000161185
WG [NCBI] 0.00014125
RPGRIP1 [NCBI] 0.000119352
RDH12 [NCBI] 8.14289e-05
CRX [NCBI] 4.86273e-05
MYO7A [NCBI] 4.48005e-05
CEP290 [NCBI] 3.72125e-05
LCA5 [NCBI] 3.42697e-05
PRL [NCBI] 3.01002e-05
LRAT [NCBI] 2.05876e-05
RPGR [NCBI] 1.86589e-05
TULP1 [NCBI] 1.7339e-05
ALMS1 [NCBI] 1.59495e-05
TIMM8A [NCBI] 1.59495e-05
GUCA1A [NCBI] 1.57049e-05
CACNA1F [NCBI] 1.51607e-05
OVOL3 [NCBI] 1.41511e-05
ANKS4B [NCBI] 1.41511e-05
USH2A [NCBI] 1.38431e-05
PAX6 [NCBI] 1.37603e-05
RLBP1 [NCBI] 1.36443e-05
LRP5 [NCBI] 1.35806e-05
RDH8 [NCBI] 1.1771e-05
ST3GAL5 [NCBI] 1.1771e-05
OVOL1 [NCBI] 1.1771e-05
OVOL2 [NCBI] 1.1771e-05
CRB2 [NCBI] 1.1771e-05
SEMA4A [NCBI] 1.1771e-05
RHO [NCBI] 1.14512e-05
PCDH21 [NCBI] 1.0873e-05
BCMO1 [NCBI] 1.02899e-05
MPDZ [NCBI] 1.02899e-05
EFHC2 [NCBI] 1.02899e-05
ABCA4 [NCBI] 1.01149e-05
RDH10 [NCBI] 9.8565e-06
DNAJC5 [NCBI] 9.22411e-06
NPHP3 [NCBI] 9.22411e-06
GNB1 [NCBI] 8.97841e-06
PDC [NCBI] 8.76365e-06
ALG3 [NCBI] 8.76365e-06
CLDN11 [NCBI] 8.76365e-06
PRPS1 [NCBI] 8.57291e-06
ATIC [NCBI] 8.40136e-06
USH1G [NCBI] 8.24549e-06
NUB1 [NCBI] 8.24549e-06
SP4 [NCBI] 7.8486e-06
POMGNT1 [NCBI] 7.8486e-06
IL1RAPL1 [NCBI] 7.73449e-06
ND4 [NCBI] 7.73449e-06
GUCA1B [NCBI] 7.62755e-06
LAMB2 [NCBI] 7.52693e-06
NRL [NCBI] 7.43193e-06
SLC4A4 [NCBI] 7.43193e-06
CNGB3 [NCBI] 7.34197e-06
KLC1 [NCBI] 7.34197e-06
INVS [NCBI] 7.09755e-06
TCIRG1 [NCBI] 7.02331e-06
OMP [NCBI] 7.02331e-06
FZD4 [NCBI] 6.81833e-06
CLN5 [NCBI] 6.81833e-06
IMPDH1 [NCBI] 6.81833e-06
ELOVL4 [NCBI] 6.75517e-06
EN2 [NCBI] 6.75517e-06
ATXN7 [NCBI] 6.69428e-06
PHYH [NCBI] 6.52376e-06
PRPF31 [NCBI] 6.41895e-06
CDH23 [NCBI] 6.41895e-06
RRM2 [NCBI] 6.27302e-06
USH1C [NCBI] 6.18231e-06
MERTK [NCBI] 6.13873e-06
ARMS2 [NCBI] 6.09625e-06
HTRA1 [NCBI] 5.6886e-06
MAOB [NCBI] 5.62408e-06
OAT [NCBI] 5.59273e-06
PITX3 [NCBI] 5.20644e-06
PPT2 [NCBI] 5.15793e-06
OPTN [NCBI] 5.15793e-06
FOXC1 [NCBI] 5.11079e-06
CTSD [NCBI] 4.99853e-06
BEST1 [NCBI] 4.89343e-06
GAA [NCBI] 4.56266e-06
ABCC6 [NCBI] 4.43475e-06
TIMP3 [NCBI] 4.41945e-06
CLN3 [NCBI] 4.16624e-06
TYRP1 [NCBI] 4.05318e-06
ADCYAP1 [NCBI] 4.02911e-06
VEGFA [NCBI] 3.86007e-06
COL2A1 [NCBI] 3.82742e-06
BSG [NCBI] 3.69627e-06
CFH [NCBI] 3.53983e-06
NOTCH3 [NCBI] 3.35053e-06
CD68 [NCBI] 2.99461e-06
FXN [NCBI] 2.96905e-06
MYOC [NCBI] 2.91587e-06
SERPINF1 [NCBI] 2.8758e-06
PRKCB [NCBI] 2.43178e-06
F8 [NCBI] 2.24587e-06
TRH [NCBI] 9.93421e-07
BDNF [NCBI] 8.02765e-07
AVP [NCBI] 6.99171e-07
NPY [NCBI] 5.08829e-07
GFAP [NCBI] 2.15594e-07
EPO [NCBI] 1.81652e-07
MS [NCBI] 2.85013e-10



OMIM


 OMIM Link Information
gain		 01
ND [NCBI] 0.00435073
LCA1 [NCBI] 0.00216552
persistent hyperplastic primary vitreous, autosomal dominant [NCBI] 0.00189724
NDP [NCBI] 0.00150973
persistent hyperplastic primary vitreous, autosomal recessive [NCBI] 0.00146205
arima syndrome [NCBI] 0.0011921
oculocerebral syndrome with hypopigmentation [NCBI] 0.0011921
MCOPS10 [NCBI] 0.000945056
SLSN3 [NCBI] 0.000945056
RP [NCBI] 0.000837497
temporal arteritis [NCBI] 0.000800602
HHG [NCBI] 0.000727474
SCAR3 [NCBI] 0.000645584
iris pigment epithelium anomalies [NCBI] 0.000645584
CND [NCBI] 0.000645584
cavitary optic disc anomalies [NCBI] 0.000592537
cataract, congenital or juvenile [NCBI] 0.000521908
RNANC [NCBI] 0.000495958
ichthyosis follicularis, atrichia, and photophobia syndrome [NCBI] 0.000495958
MCOP1 [NCBI] 0.000437344
ehlers-danlos syndrome, type vib [NCBI] 0.000421973
ALMS [NCBI] 0.00042143
leber optic atrophy, susceptibility to [NCBI] 0.000372708
lymphedema, microcephaly, chorioretinopathy syndrome [NCBI] 0.000362597
LCA2 [NCBI] 0.000321229
OPPG [NCBI] 0.000312558
GUCY2D [NCBI] 0.000311392
SLSN1 [NCBI] 0.00028455
JBTS1 [NCBI] 0.00028242
RPE65 [NCBI] 0.000251719
SLE [NCBI] 0.00024433
leber optic atrophy [NCBI] 0.000239966
MTS [NCBI] 0.000162593
LCA4 [NCBI] 0.000160481
CRB1 [NCBI] 0.000153463
PRD [NCBI] 0.000146535
klippel-trenaunay-weber syndrome [NCBI] 0.000138113
glaucoma, normal tension, susceptibility to [NCBI] 0.000123724
RDH12 [NCBI] 0.000123692
usher syndrome, type i [NCBI] 0.000121246
STL1 [NCBI] 0.000117321
EVR2 [NCBI] 0.000114419
NPHP4 [NCBI] 0.000104732
USH3 [NCBI] 0.000101403
SCA7 [NCBI] 9.90398e-05
cortical blindness, retardation, and postaxial polydactyly [NCBI] 9.56626e-05
aicar transformylase/imp cyclohydrolase, deficiency of [NCBI] 9.56626e-05
RP35 [NCBI] 9.56626e-05
CORD10 [NCBI] 9.56626e-05
pseudoglaucoma [NCBI] 9.56626e-05
rodrigues blindness [NCBI] 9.56626e-05
amaurosis congenita, cone-rod type, with congenital hypertrichosis [NCBI] 9.56626e-05
RPGRIP1 [NCBI] 9.29831e-05
septooptic dysplasia [NCBI] 9.0312e-05
CRX [NCBI] 8.56809e-05
PRL [NCBI] 8.00068e-05
ehlers-danlos syndrome, type vi [NCBI] 7.94316e-05
NPHP1 [NCBI] 7.3514e-05
amish infantile epilepsy syndrome [NCBI] 7.32343e-05
NFRCD [NCBI] 7.32343e-05
MSS [NCBI] 7.14392e-05
ATIC [NCBI] 7.12884e-05
SEDC [NCBI] 6.68106e-05
MYO7A [NCBI] 6.67082e-05
GLC1A [NCBI] 6.59662e-05
retinohepatoendocrinologic syndrome [NCBI] 6.47964e-05
LCA10 [NCBI] 6.47964e-05
ARTS [NCBI] 6.47964e-05
oculocerebral hypopigmentation syndrome of preus [NCBI] 6.47964e-05
osteopetrosis and infantile neuroaxonal dystrophy [NCBI] 6.47964e-05
coloboma of optic nerve [NCBI] 6.47964e-05
yemenite deaf-blind hypopigmentation syndrome [NCBI] 6.47964e-05
MAOA [NCBI] 5.99564e-05
CSNBAD1 [NCBI] 5.93324e-05
LCA5 [NCBI] 5.93324e-05
internal carotid artery, spontaneous dissection of [NCBI] 5.93324e-05
spastic ataxia [NCBI] 5.93324e-05
USH1G [NCBI] 5.93324e-05
CLN10 [NCBI] 5.93324e-05
leber congenital amaurosis, type iii [NCBI] 5.93324e-05
ST3GAL5 [NCBI] 5.75153e-05
OPN4 [NCBI] 5.75153e-05
CNGA1 [NCBI] 5.75153e-05
RPGR [NCBI] 5.73024e-05
OPTB2 [NCBI] 5.52808e-05
coats disease [NCBI] 5.52808e-05
TST [NCBI] 5.23214e-05
SLC4A7 [NCBI] 5.23214e-05
LCA5 [NCBI] 5.23214e-05
DNAJC5 [NCBI] 5.23214e-05
musical perfect pitch [NCBI] 4.93909e-05
CSNB1B [NCBI] 4.93909e-05
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation [NCBI] 4.93909e-05
USH1G [NCBI] 4.89512e-05
SLC4A4 [NCBI] 4.89512e-05
CNGB1 [NCBI] 4.89512e-05
LRAT [NCBI] 4.89512e-05
ARL6 [NCBI] 4.89512e-05
SEMA4A [NCBI] 4.89512e-05
CLN5 [NCBI] 4.89512e-05
adenylosuccinase deficiency [NCBI] 4.71115e-05
PDC [NCBI] 4.64471e-05
RHO [NCBI] 4.63381e-05
NPHP3 [NCBI] 4.51242e-05
RP12 [NCBI] 4.51242e-05
VLDLRCH [NCBI] 4.51242e-05
NPHP2 [NCBI] 4.51242e-05
NPHP3 [NCBI] 4.4453e-05
IMPDH1 [NCBI] 4.4453e-05
sarcosinemia [NCBI] 4.33636e-05
fundus albipunctatus [NCBI] 4.33636e-05
USH3A [NCBI] 4.27961e-05
sturge-weber syndrome [NCBI] 4.17842e-05
CLN5 [NCBI] 4.03528e-05
ALMS1 [NCBI] 4.01405e-05
TTC10 [NCBI] 4.01405e-05
STGD3 [NCBI] 3.90446e-05
WZS [NCBI] 3.90446e-05
USH1C [NCBI] 3.90446e-05
CEP290 [NCBI] 3.80532e-05
TIMM8A [NCBI] 3.80532e-05
OPTA2 [NCBI] 3.78408e-05
SFD [NCBI] 3.67262e-05
CTSD [NCBI] 3.55763e-05
COL11A1 [NCBI] 3.55763e-05
TIMP1 [NCBI] 3.48732e-05
synovitis, granulomatous, with uveitis and cranial neuropathies [NCBI] 3.47195e-05
pseudoxanthoma elasticum, forme fruste [NCBI] 3.47195e-05
RLBP1 [NCBI] 3.24811e-05
ESCS [NCBI] 3.21438e-05
MAOB [NCBI] 3.19653e-05
CLN2 [NCBI] 3.06494e-05
OMP [NCBI] 3.01406e-05
BBS [NCBI] 2.99548e-05
SOX10 [NCBI] 2.97339e-05
MTND1 [NCBI] 2.86083e-05
EVR1 [NCBI] 2.80603e-05
STGD1 [NCBI] 2.63901e-05
PPT1 [NCBI] 2.56009e-05
ornithine aminotransferase deficiency [NCBI] 2.53469e-05
RS1 [NCBI] 2.53469e-05
OPA1 [NCBI] 2.49005e-05
myoclonic epilepsy of lafora [NCBI] 2.44382e-05
MSD [NCBI] 2.39913e-05
SHH [NCBI] 2.38599e-05
CADASIL [NCBI] 2.234e-05
MEB [NCBI] 2.234e-05
MTND4 [NCBI] 2.20137e-05
BSG [NCBI] 2.15038e-05
walker-warburg syndrome [NCBI] 2.12254e-05
OCA1A [NCBI] 2.05326e-05
VMD [NCBI] 1.98759e-05
FDH [NCBI] 1.98759e-05
WFS1 [NCBI] 1.95599e-05
COL2A1 [NCBI] 1.88102e-05
MYOC [NCBI] 1.67496e-05
FCMD [NCBI] 1.65376e-05
metachromatic leukodystrophy [NCBI] 1.26809e-05
PEDF [NCBI] 1.24165e-05
KLK3 [NCBI] 1.02479e-05
VRNI [NCBI] 8.35077e-06
VHL [NCBI] 6.41192e-06
GNRH1 [NCBI] 5.99991e-06
EV [NCBI] 4.63995e-06
VEGF [NCBI] 3.67652e-06
panencephalitis, subacute sclerosing [NCBI] 2.84154e-06
EPO [NCBI] 1.89358e-06
PJS [NCBI] 1.77364e-06
GFAP [NCBI] 1.60878e-06
PXE [NCBI] 1.49579e-06
TS [NCBI] 1.31107e-06
AVP [NCBI] 5.01171e-07
G6PD [NCBI] 3.09291e-07
ALD [NCBI] 2.07354e-07
NPY [NCBI] 1.84224e-07
BDNF [NCBI] 7.78476e-08



Database Center for Life Science