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01 Macula Lutea [NCBI]

Gene


 Gene Link Information
Gain		 01
LOC152905 [NCBI] 0.000419965
OED [NCBI] 0.000348046
CACD [NCBI] 0.000257177
MS [NCBI] 0.000256993
ABCA4 [NCBI] 2.57456e-05
PRPH2 [NCBI] 1.39361e-05
VEGFA [NCBI] 1.30864e-05
BEST1 [NCBI] 1.24102e-05
CFH [NCBI] 1.14907e-05
RLBP1 [NCBI] 1.0701e-05
SERPINF1 [NCBI] 8.82362e-06
CERKL [NCBI] 8.09226e-06
ELOVL4 [NCBI] 6.52465e-06
CNGB3 [NCBI] 6.52465e-06
EFEMP1 [NCBI] 6.47914e-06
CFB [NCBI] 6.47914e-06
RDH5 [NCBI] 6.43562e-06
RTN1 [NCBI] 6.2783e-06
RTN3 [NCBI] 6.20805e-06
APOE [NCBI] 6.0737e-06
CRYAA [NCBI] 5.995e-06
ROR2 [NCBI] 5.94163e-06
OCA2 [NCBI] 5.94163e-06
SMPD1 [NCBI] 5.91598e-06
MSRA [NCBI] 5.01265e-06
RPGR [NCBI] 4.93389e-06
TIMP3 [NCBI] 4.83485e-06
TLR3 [NCBI] 3.87099e-06
ICAM1 [NCBI] 3.86775e-06
GSTP1 [NCBI] 3.70163e-06
ATM [NCBI] 3.59809e-06
ENG [NCBI] 3.59075e-06
HMOX1 [NCBI] 3.13215e-06
PAX6 [NCBI] 2.85461e-06
GFAP [NCBI] 1.53347e-06



OMIM


 OMIM Link Information
gain		 01
VRNI [NCBI] 0.00488535
MCDR1 [NCBI] 0.00266803
retinoschisis of fovea [NCBI] 0.00240833
CORD7 [NCBI] 0.00198097
dilution, pigmentary [NCBI] 0.000890498
VMD [NCBI] 0.000847454
ARMD1 [NCBI] 0.000784048
macular dystrophy, butterfly-shaped pigmentary, 2 [NCBI] 0.000774164
coloboma of macula with type b brachydactyly [NCBI] 0.000745195
STGD1 [NCBI] 0.000723037
cavitary optic disc anomalies [NCBI] 0.000698985
RCD1 [NCBI] 0.000643352
macular edema, cystoid [NCBI] 0.000599231
neuraminidase deficiency [NCBI] 0.000598529
MYP2 [NCBI] 0.000480617
foveal hypoplasia and presenile cataract syndrome [NCBI] 0.000440581
RP [NCBI] 0.000381221
macular dystrophy, vitelliform, adult-onset [NCBI] 0.000253344
SLS [NCBI] 0.000233614
BDB1 [NCBI] 0.00023034
STGD3 [NCBI] 0.000224387
alport syndrome, autosomal dominant [NCBI] 0.000223065
DHRD [NCBI] 0.000219009
ACHM2 [NCBI] 0.000219009
AIED [NCBI] 0.000205432
mesangial sclerosis, diffuse renal, with ocular abnormalities [NCBI] 0.000185704
coloboma of macula and skeletal anomalies [NCBI] 0.000185704
ARMD2 [NCBI] 0.000146467
macular dystrophy, concentric annular [NCBI] 0.000146467
AN2 [NCBI] 0.000141686
grouped pigmentation of the macula [NCBI] 0.000131682
keratitis, hereditary [NCBI] 0.000131682
coloboma of optic nerve [NCBI] 0.000122094
neuraminidase deficiency with beta-galactosidase deficiency [NCBI] 0.000113064
cherubism [NCBI] 0.000109311
patterned dystrophy of retinal pigment epithelium [NCBI] 0.000104607
PAX6 [NCBI] 0.000102898
ELOVL4 [NCBI] 9.98349e-05
ACHM3 [NCBI] 9.70746e-05
diabetes-deafness syndrome, maternally transmitted [NCBI] 9.39602e-05
SFD [NCBI] 8.86231e-05
gm1-gangliosidosis, type ii [NCBI] 8.62994e-05
MCDC1 [NCBI] 8.62994e-05
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency [NCBI] 8.41579e-05
CORDX1 [NCBI] 8.41579e-05
PRPH2 [NCBI] 7.77799e-05
gm1-gangliosidosis, type iii [NCBI] 7.54284e-05
robinow syndrome, autosomal recessive [NCBI] 7.25995e-05
ESCS [NCBI] 7.25995e-05
hyperoxaluria, primary, type i [NCBI] 7.25995e-05
MELAS [NCBI] 7.00417e-05
EVR1 [NCBI] 6.77088e-05
RHO [NCBI] 5.74186e-05
ABL [NCBI] 5.61689e-05
SCA7 [NCBI] 5.61689e-05
retinal arteries, tortuosity of [NCBI] 4.73473e-05
RTN3 [NCBI] 4.28747e-05
tritanopia [NCBI] 4.28747e-05
SAG [NCBI] 4.18434e-05
CACNA1F [NCBI] 3.81664e-05
ROR2 [NCBI] 3.70991e-05
panencephalitis, subacute sclerosing [NCBI] 3.70579e-05
SMPD1 [NCBI] 3.49701e-05
TIMP3 [NCBI] 3.36303e-05
ABCA4 [NCBI] 3.19987e-05
IP [NCBI] 3.02887e-05
RS1 [NCBI] 2.99067e-05
MTTL1 [NCBI] 2.82919e-05
VEGF [NCBI] 2.62132e-05
APOE [NCBI] 6.53776e-06
VIP [NCBI] 1.69583e-06
GFAP [NCBI] 1.36768e-06



Database Center for Life Science