Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Fovea Centralis [NCBI]


Gene


Gene Link Information
Gain
01
OED [NCBI] 0.000394226
MS [NCBI] 0.000155008
VEGFA [NCBI] 4.30655e-05
PAX6 [NCBI] 3.43403e-05
ABCA4 [NCBI] 1.84727e-05
PRPH2 [NCBI] 1.39925e-05
ROM1 [NCBI] 1.36037e-05
OPN1MW [NCBI] 7.2701e-06
MFRP [NCBI] 7.17897e-06
FGFRL1 [NCBI] 7.17897e-06
PDE6C [NCBI] 7.01838e-06
CFB [NCBI] 6.50695e-06
NR2E3 [NCBI] 6.20249e-06
HPS1 [NCBI] 6.05059e-06
GPR143 [NCBI] 5.91876e-06
NDP [NCBI] 5.64031e-06
GRK1 [NCBI] 5.62179e-06
CHM [NCBI] 5.48484e-06
OAT [NCBI] 5.23184e-06
CFH [NCBI] 5.06111e-06
FGFR4 [NCBI] 5.01013e-06
GFAP [NCBI] 4.44916e-06
ANGPT1 [NCBI] 4.30618e-06
CP [NCBI] 4.17778e-06
FGFR3 [NCBI] 3.71563e-06
ATM [NCBI] 3.62563e-06
IL6 [NCBI] 2.83388e-06
PCNA [NCBI] 1.77352e-06
FASLG [NCBI] 1.73049e-06




OMIM


OMIM Link Information
gain
01
retinoschisis of fovea [NCBI] 0.00294936
MCDR1 [NCBI] 0.00260942
foveal hypoplasia and presenile cataract syndrome [NCBI] 0.00128892
RP [NCBI] 0.00106917
macular dystrophy, butterfly-shaped pigmentary, 2 [NCBI] 0.00103446
NNO1 [NCBI] 0.00085732
MYP2 [NCBI] 0.000735764
macular dystrophy, vitelliform, adult-onset [NCBI] 0.000719458
AN2 [NCBI] 0.000327878
OCA1A [NCBI] 0.000228218
microphthalmia, posterior, with retinitis pigmentosa, foveoschisis, and optic disc drusen [NCBI] 0.000212159
PAX6 [NCBI] 0.000198952
VRNI [NCBI] 0.000188485
PRPH2 [NCBI] 0.000183517
patterned dystrophy of retinal pigment epithelium [NCBI] 0.000130915
AIED [NCBI] 0.000108284
VMD [NCBI] 8.83909e-05
SLS [NCBI] 7.24172e-05
IP [NCBI] 5.42413e-05
MFRP [NCBI] 4.68655e-05
VEGF [NCBI] 4.58546e-05
ABCA4 [NCBI] 3.33311e-05
OA1 [NCBI] 3.30919e-05
RS1 [NCBI] 3.12374e-05
RP2 [NCBI] 2.96207e-05
RHO [NCBI] 2.49277e-05
CP [NCBI] 1.93018e-05
GFAP [NCBI] 1.1396e-05
PCNA [NCBI] 3.25618e-06




Database Center for Life Science