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MeSH keywords -> Related genes, diseases (OMIM)


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01 Optic Atrophies, Hereditary [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 0.00064961
SPOAN [NCBI] 0.000327954
OPA4 [NCBI] 0.000267232
GUCY2D [NCBI] 0.000164983
OPA1 [NCBI] 0.000123647
RPE65 [NCBI] 8.40755e-05
OPA3 [NCBI] 3.65135e-05
AIPL1 [NCBI] 3.23083e-05
RPGRIP1 [NCBI] 3.1981e-05
CRB1 [NCBI] 3.04797e-05
NRL [NCBI] 2.19276e-05
CRX [NCBI] 2.06648e-05
GUCA1A [NCBI] 2.02899e-05
ZFP90 [NCBI] 1.64373e-05
DGKG [NCBI] 1.25752e-05
SERPINF1 [NCBI] 1.2519e-05
CASK [NCBI] 1.21414e-05
AP1S2 [NCBI] 1.17958e-05
IMPG1 [NCBI] 1.15084e-05
LCA5 [NCBI] 1.15084e-05
NDUFA1 [NCBI] 1.15084e-05
ALG3 [NCBI] 1.10472e-05
PRPS1 [NCBI] 1.08562e-05
GABRR2 [NCBI] 1.02528e-05
RDH12 [NCBI] 1.01302e-05
DLG4 [NCBI] 9.37647e-06
DLG1 [NCBI] 9.16187e-06
RP2 [NCBI] 8.20791e-06
MFN2 [NCBI] 8.09623e-06
HES1 [NCBI] 7.37306e-06
BEST1 [NCBI] 7.15236e-06
RCVRN [NCBI] 7.01334e-06
CS [NCBI] 6.50631e-06




OMIM


OMIM Link Information
gain
01
leber optic atrophy, susceptibility to [NCBI] 0.0130652
leber optic atrophy [NCBI] 0.00842751
MTND4 [NCBI] 0.00308361
OPA4 [NCBI] 0.00146918
SPOAN [NCBI] 0.000993831
OPA1 [NCBI] 0.000832977
MTND1 [NCBI] 0.000678535
MTND6 [NCBI] 0.000644064
arima syndrome [NCBI] 0.000521852
LCA1 [NCBI] 0.000472552
GUCY2D [NCBI] 0.000448928
MTND5 [NCBI] 0.000372107
LCA4 [NCBI] 0.000316582
RPE65 [NCBI] 0.00019324
MTCYB [NCBI] 0.000188549
OPA1 [NCBI] 0.000184358
MTND2 [NCBI] 0.000174478
dystonia, familial, with visual failure and striatal lucencies [NCBI] 0.000149119
3-@methylglutaconic aciduria, type iii [NCBI] 0.000143165
wolfram syndrome, mitochondrial form [NCBI] 0.000138151
MTCO1 [NCBI] 0.000133533
optic atrophy with negative electroretinograms [NCBI] 0.000105405
optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant [NCBI] 0.000105405
MTCO3 [NCBI] 9.90938e-05
NRL [NCBI] 9.40846e-05
RPGRIP1 [NCBI] 9.40846e-05
KSS [NCBI] 8.08037e-05
optic atrophy 3, autosomal dominant [NCBI] 7.44991e-05
ARTS [NCBI] 7.44991e-05
CASK [NCBI] 7.18383e-05
LCA5 [NCBI] 6.9015e-05
leber congenital amaurosis, type iii [NCBI] 6.9015e-05
CORD6 [NCBI] 6.9015e-05
MRX59 [NCBI] 6.49433e-05
LCA2 [NCBI] 6.17035e-05
DGKG [NCBI] 5.80647e-05
HES1 [NCBI] 5.80647e-05
RP12 [NCBI] 5.47064e-05
OPA3 [NCBI] 5.28704e-05
TST [NCBI] 5.28704e-05
LCA5 [NCBI] 5.28704e-05
AP1S2 [NCBI] 4.94998e-05
DLG4 [NCBI] 4.94998e-05
MERRF [NCBI] 4.85465e-05
SNDI [NCBI] 4.85465e-05
CORD2 [NCBI] 4.32112e-05
AIPL1 [NCBI] 4.19257e-05
GUCA1A [NCBI] 4.19257e-05
PRPS1 [NCBI] 4.19257e-05
RP [NCBI] 4.06959e-05
CRB1 [NCBI] 3.95875e-05
CRX [NCBI] 3.61208e-05
MFN2 [NCBI] 3.30236e-05
MTTK [NCBI] 2.75222e-05
MTATP6 [NCBI] 2.56334e-05
MTTL1 [NCBI] 1.8851e-05
PEDF [NCBI] 1.2903e-05




Database Center for Life Science