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01 Vision Disorders [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.00188542
RCD2 [NCBI] 0.000287562
PPR [NCBI] 8.30019e-05
WG [NCBI] 7.4155e-05
OPA1 [NCBI] 4.42672e-05
RCVRN [NCBI] 3.43363e-05
PRL [NCBI] 3.2218e-05
TIMM8A [NCBI] 3.04207e-05
RGS9BP [NCBI] 2.78948e-05
RGS9 [NCBI] 2.78948e-05
CHM [NCBI] 2.55341e-05
MYO7A [NCBI] 2.30323e-05
NR2E3 [NCBI] 1.8936e-05
CACNA1F [NCBI] 1.80159e-05
OPTN [NCBI] 1.55425e-05
RHO [NCBI] 1.42893e-05
NOTCH3 [NCBI] 1.18127e-05
CASP8AP2 [NCBI] 1.12822e-05
TGFBI [NCBI] 1.11785e-05
PAX6 [NCBI] 1.06003e-05
VPS13B [NCBI] 1.04034e-05
PDE5A [NCBI] 1.03294e-05
PRPS1 [NCBI] 9.99738e-06
PRKCB [NCBI] 9.85526e-06
OPA3 [NCBI] 9.27179e-06
LAMB2 [NCBI] 8.94935e-06
TULP1 [NCBI] 8.8541e-06
DLAT [NCBI] 8.76388e-06
PRPF8 [NCBI] 8.59658e-06
NYX [NCBI] 8.44421e-06
OPHN1 [NCBI] 8.44421e-06
CLCN7 [NCBI] 8.37283e-06
CRX [NCBI] 8.23846e-06
IMPDH1 [NCBI] 8.23846e-06
ELOVL4 [NCBI] 8.17504e-06
ALMS1 [NCBI] 8.17504e-06
EFEMP1 [NCBI] 7.99781e-06
ITM2B [NCBI] 7.88913e-06
CPE [NCBI] 7.69059e-06
CA2 [NCBI] 7.69059e-06
GPR143 [NCBI] 7.47111e-06
RP2 [NCBI] 7.35184e-06
EDNRA [NCBI] 7.31387e-06
CD3E [NCBI] 7.27674e-06
MFN2 [NCBI] 7.24039e-06
USH2A [NCBI] 7.13581e-06
OCRL [NCBI] 6.97467e-06
PPT1 [NCBI] 6.79957e-06
EDNRB [NCBI] 6.79957e-06
BEST1 [NCBI] 6.29924e-06
GJA1 [NCBI] 5.998e-06
POLG [NCBI] 5.89764e-06
ABCC6 [NCBI] 5.83392e-06
RPL22 [NCBI] 5.77254e-06
RPGR [NCBI] 5.74267e-06
PAX2 [NCBI] 5.64215e-06
LCAT [NCBI] 5.47015e-06
MIF [NCBI] 5.28028e-06
ABCA4 [NCBI] 5.28028e-06
CRH [NCBI] 5.21433e-06
JAG1 [NCBI] 4.8399e-06
TOR1A [NCBI] 4.82282e-06
EDN1 [NCBI] 4.78917e-06
CYP1B1 [NCBI] 4.72388e-06
ESR2 [NCBI] 4.52102e-06
CD44 [NCBI] 4.38554e-06
PSEN1 [NCBI] 4.36617e-06
MYOC [NCBI] 4.27261e-06
CYP2C19 [NCBI] 4.2015e-06
CYP2C9 [NCBI] 4.15015e-06
ICAM1 [NCBI] 4.12785e-06
PRNP [NCBI] 3.8445e-06
BTK [NCBI] 3.78092e-06
ABCB1 [NCBI] 3.24093e-06
MOG [NCBI] 2.88455e-06
GJB2 [NCBI] 2.87222e-06
VHL [NCBI] 2.7363e-06
ESR1 [NCBI] 2.72516e-06
CST3 [NCBI] 2.52639e-06
VIP [NCBI] 2.27096e-06
TRH [NCBI] 2.15837e-06
NOS3 [NCBI] 1.69542e-06
NPY [NCBI] 1.53481e-06
NOS2 [NCBI] 1.5152e-06
NGF [NCBI] 1.01689e-06
APOE [NCBI] 7.74657e-07
PTGS2 [NCBI] 4.0818e-07
EGF [NCBI] 3.33091e-07



OMIM


 OMIM Link Information
gain		 01
behr syndrome [NCBI] 0.00152161
cavitary optic disc anomalies [NCBI] 0.00138638
strabismus, susceptibility to [NCBI] 0.00107507
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.000924208
unique green phenomenon [NCBI] 0.000907885
GLC1F [NCBI] 0.000907885
temporal arteritis [NCBI] 0.000903688
leber optic atrophy, susceptibility to [NCBI] 0.000901326
blepharophimosis with ptosis, syndactyly, and short stature [NCBI] 0.000690406
retinal cone dystrophy 2 [NCBI] 0.000690406
mental retardation with optic atrophy, deafness, and seizures [NCBI] 0.000608619
CORD5 [NCBI] 0.000555675
VRCP [NCBI] 0.000555675
ectopia lentis with ectopia of pupil [NCBI] 0.000555675
RP [NCBI] 0.000527786
ichthyosis follicularis, atrichia, and photophobia syndrome [NCBI] 0.000459406
CMM [NCBI] 0.000450915
ocular motor apraxia [NCBI] 0.000437349
CDB2 [NCBI] 0.000418126
leber optic atrophy [NCBI] 0.000377128
VRNI [NCBI] 0.000362511
PPR [NCBI] 0.000175114
CF [NCBI] 0.000166694
CMTX5 [NCBI] 0.000155007
kabuki syndrome [NCBI] 0.000150501
STGD1 [NCBI] 0.000144479
foveal hypoplasia and presenile cataract syndrome [NCBI] 0.000132166
POAG [NCBI] 0.000131004
panencephalitis, subacute sclerosing [NCBI] 0.000128081
PRL [NCBI] 0.000117911
neuraminidase deficiency [NCBI] 0.000114761
CJD [NCBI] 0.000114621
CBP [NCBI] 0.000102103
PERRS [NCBI] 9.98991e-05
fourth cranial nerve palsy, familial congenital [NCBI] 9.98991e-05
OOCH [NCBI] 9.98991e-05
cholestasis with gallstone, ataxia, and visual disturbance [NCBI] 9.98991e-05
reese retinal dysplasia [NCBI] 9.98991e-05
CLN1 [NCBI] 8.6399e-05
RGS9BP [NCBI] 8.08766e-05
RGS9 [NCBI] 8.08766e-05
gaucher disease, type iii [NCBI] 8.06549e-05
SLE [NCBI] 7.9879e-05
OPA1 [NCBI] 7.96253e-05
retinopathy, pericentral pigmentary, autosomal recessive [NCBI] 7.74605e-05
COH1 [NCBI] 7.01502e-05
OCA1A [NCBI] 7.01502e-05
optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive [NCBI] 6.90124e-05
ARTS [NCBI] 6.90124e-05
arhinia, choanal atresia, and microphthalmia [NCBI] 6.90124e-05
coloboma of optic nerve [NCBI] 6.90124e-05
AN2 [NCBI] 6.47681e-05
PRD [NCBI] 6.35382e-05
pseudopapilledema [NCBI] 5.94763e-05
DLAT [NCBI] 5.85252e-05
dystonia, familial, with visual failure and striatal lucencies [NCBI] 5.62463e-05
nonarteritic anterior ischemic optic neuropathy, susceptibility to [NCBI] 5.62463e-05
oguchi disease [NCBI] 5.62463e-05
IFNA2 [NCBI] 5.40176e-05
NTF3 [NCBI] 5.40176e-05
PPCRA [NCBI] 5.3566e-05
tritanopia [NCBI] 5.2356e-05
rheumatoid arthritis, systemic juvenile [NCBI] 5.12764e-05
TUB [NCBI] 5.09339e-05
EPAS1 [NCBI] 5.09339e-05
PRPS1 [NCBI] 5.09339e-05
NYS1 [NCBI] 4.92788e-05
ELOVL4 [NCBI] 4.8587e-05
PXE [NCBI] 4.82751e-05
TIMM8A [NCBI] 4.75941e-05
pierson syndrome [NCBI] 4.7508e-05
CLCN7 [NCBI] 4.6692e-05
amyloidosis vii [NCBI] 4.59184e-05
macular dystrophy, vitelliform, adult-onset [NCBI] 4.59184e-05
CACNA1F [NCBI] 4.58656e-05
CRX [NCBI] 4.5103e-05
schwannomatosis [NCBI] 4.44767e-05
antiphospholipid syndrome [NCBI] 4.44767e-05
CDA [NCBI] 4.19443e-05
NF1 [NCBI] 4.18096e-05
MTND5 [NCBI] 4.09693e-05
SFD [NCBI] 4.08195e-05
MTS [NCBI] 3.97721e-05
FRDA [NCBI] 3.97222e-05
XPC [NCBI] 3.84342e-05
krabbe disease [NCBI] 3.82909e-05
CORD2 [NCBI] 3.78724e-05
DHRD [NCBI] 3.78724e-05
CPE [NCBI] 3.70481e-05
ESCS [NCBI] 3.61859e-05
PDHA1 [NCBI] 3.6124e-05
OPTN [NCBI] 3.58345e-05
DLB [NCBI] 3.54092e-05
PRPH2 [NCBI] 3.528e-05
ABCA4 [NCBI] 3.40181e-05
deafness, conductive, with stapes fixation [NCBI] 3.39681e-05
CSNB1A [NCBI] 3.32971e-05
USH2A [NCBI] 3.32971e-05
refsum disease [NCBI] 3.26556e-05
PSNP1 [NCBI] 3.20411e-05
ALMS [NCBI] 3.14516e-05
MTND4 [NCBI] 3.13465e-05
RPGR [NCBI] 3.11686e-05
PAX6 [NCBI] 3.06539e-05
alzheimer disease 3 [NCBI] 3.03402e-05
camurati-engelmann disease [NCBI] 2.98152e-05
ABCD1 [NCBI] 2.97006e-05
MTHFR [NCBI] 2.94028e-05
RP3 [NCBI] 2.93089e-05
DYX1 [NCBI] 2.93089e-05
mucolipidosis iv [NCBI] 2.882e-05
factor v deficiency [NCBI] 2.8039e-05
OCRL [NCBI] 2.78902e-05
mucopolysaccharidosis type vi [NCBI] 2.78902e-05
TGD [NCBI] 2.74475e-05
usher syndrome, type i [NCBI] 2.70184e-05
ODDD [NCBI] 2.70184e-05
CADASIL [NCBI] 2.61981e-05
MEB [NCBI] 2.61981e-05
RHO [NCBI] 2.56882e-05
walker-warburg syndrome [NCBI] 2.50527e-05
ALD [NCBI] 2.47895e-05
GCPS [NCBI] 2.36623e-05
WFS1 [NCBI] 2.33361e-05
melanoma, uveal [NCBI] 2.2707e-05
CDG1A [NCBI] 2.24034e-05
PSEN1 [NCBI] 2.19787e-05
CLN3 [NCBI] 2.15328e-05
CSA [NCBI] 2.12551e-05
CHM [NCBI] 2.09834e-05
BPES [NCBI] 2.04566e-05
SCA7 [NCBI] 2.02013e-05
NF2 [NCBI] 1.85467e-05
TS [NCBI] 1.76019e-05
OCP [NCBI] 1.63322e-05
APOE [NCBI] 1.07798e-05
CDLS1 [NCBI] 1.05181e-05
thrombocytopenic purpura, autoimmune [NCBI] 1.02393e-05
BBS [NCBI] 9.43112e-06
SMAX1 [NCBI] 7.90505e-06
VIP [NCBI] 5.52252e-06
PD [NCBI] 3.41118e-06
MFS [NCBI] 2.65594e-06
NPY [NCBI] 2.3605e-06
AD [NCBI] 1.91842e-06
PWS [NCBI] 1.2357e-06
amyloidosis vi [NCBI] 1.16997e-06
FMF [NCBI] 7.27525e-07
NGFB [NCBI] 6.60907e-07
EGF [NCBI] 3.07512e-07
VEGF [NCBI] 1.79554e-07
GTS [NCBI] 1.66276e-07



Database Center for Life Science