Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Fovea Centralis	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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