Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Aniridia	[NCBI]

Gene	Link	Information Gain
PAX6	[NCBI]	0.00160362
H19	[NCBI]	0.000312204
ELP4	[NCBI]	2.69882e-05
FOXC1	[NCBI]	1.45437e-05
PAX2	[NCBI]	1.27732e-05
PAX5	[NCBI]	1.23015e-05
RCN1	[NCBI]	1.12649e-05
OTX2	[NCBI]	8.06878e-06
PAX1	[NCBI]	7.99436e-06
PAX4	[NCBI]	7.24151e-06
PAX9	[NCBI]	6.65415e-06
SAA1	[NCBI]	6.62138e-06
PAX7	[NCBI]	6.46644e-06
GCH1	[NCBI]	6.40824e-06
CAT	[NCBI]	5.16231e-06
PAX8	[NCBI]	5.09065e-06
WT1	[NCBI]	4.62882e-06
UMOD	[NCBI]	3.02839e-06
BCR	[NCBI]	2.75392e-06
ADA	[NCBI]	2.09151e-06
VEGFA	[NCBI]	6.29718e-07

OMIM	Link	Information gain
aniridia, cerebellar ataxia, and mental deficiency	[NCBI]	0.00335645
AN2	[NCBI]	0.00310653
PAX6	[NCBI]	0.00232631
GUD	[NCBI]	0.00022421
AN1	[NCBI]	0.000182269
wagr syndrome	[NCBI]	0.000167573
ectopia pupillae	[NCBI]	0.000127341
WT1	[NCBI]	9.7471e-05
keratitis, hereditary	[NCBI]	8.68069e-05
ELP4	[NCBI]	8.21209e-05
foveal hypoplasia and presenile cataract syndrome	[NCBI]	8.08408e-05
RCN1	[NCBI]	6.83427e-05
PAX4	[NCBI]	6.31438e-05
PAX7	[NCBI]	6.31438e-05
neuroblastoma stage 4s gene	[NCBI]	5.72593e-05
PAX1	[NCBI]	5.09324e-05
PAX9	[NCBI]	4.98282e-05
PAX5	[NCBI]	4.79325e-05
PAX8	[NCBI]	4.56347e-05
PAX2	[NCBI]	4.12862e-05
VHL	[NCBI]	3.32066e-05
CAT	[NCBI]	2.11697e-05
ADA	[NCBI]	7.64991e-06
VEGF	[NCBI]	3.23545e-06