Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Astigmatism [NCBI]

Gene


 Gene Link Information
Gain		 01
FGFR3 [NCBI] 1.78704e-05
KERA [NCBI] 1.31484e-05
HPS1 [NCBI] 1.14481e-05
ALDH3A2 [NCBI] 1.12332e-05
TWIST1 [NCBI] 9.57397e-06
FGFR2 [NCBI] 9.21896e-06
TGFBI [NCBI] 8.75392e-06
NGF [NCBI] 4.98484e-06



OMIM


 OMIM Link Information
gain		 01
astigmatism [NCBI] 0.00342502
microcoria, congenital [NCBI] 0.00111789
vitreoretinal degeneration, snowflake type [NCBI] 0.000817902
HYPX [NCBI] 0.000625244
ADFN [NCBI] 0.00059223
sjogren syndrome [NCBI] 0.000541934
AIED [NCBI] 0.000192944
SLS [NCBI] 0.00014641
SCRA [NCBI] 0.000104439
corneal dystrophy, juvenile epithelial, of meesmann [NCBI] 0.000101727
HRD [NCBI] 9.39491e-05
KCS [NCBI] 9.39491e-05
papillorenal syndrome [NCBI] 8.56759e-05
KTCN1 [NCBI] 8.31153e-05
CACNA1F [NCBI] 7.92643e-05
FIH [NCBI] 7.37888e-05
DGS [NCBI] 4.80254e-05
NGFB [NCBI] 2.75901e-05
RP [NCBI] 2.7424e-05



Database Center for Life Science