Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Aniridia [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science