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MeSH keywords -> Related genes, diseases (OMIM)


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01 Amblyopia [NCBI]

Gene


 Gene Link Information
Gain		 01
PPR [NCBI] 0.000208982
MS [NCBI] 3.75925e-05
NYX [NCBI] 1.47246e-05
PDE6B [NCBI] 1.35162e-05
TWIST1 [NCBI] 1.14692e-05
FGFR3 [NCBI] 9.51592e-06
NGF [NCBI] 6.85806e-06



OMIM


 OMIM Link Information
gain		 01
HFH [NCBI] 0.0022583
arteriosclerosis, severe juvenile [NCBI] 0.00111789
vitreoretinal degeneration, snowflake type [NCBI] 0.000817902
distichiasis [NCBI] 0.000724991
duane retraction syndrome 2 [NCBI] 0.000667246
iminoglycinuria [NCBI] 0.000607858
DURS1 [NCBI] 0.000531565
PPR [NCBI] 0.000369215
CFEOM1 [NCBI] 0.00020285
mental and growth retardation with amblyopia [NCBI] 0.000125783
corneal dystrophy, juvenile epithelial, of meesmann [NCBI] 0.000101727
AN1 [NCBI] 9.94045e-05
EVR1 [NCBI] 7.95849e-05
apert syndrome [NCBI] 7.37888e-05
AN2 [NCBI] 6.85485e-05
MTND4 [NCBI] 6.46273e-05
SLS [NCBI] 6.10389e-05
leber optic atrophy [NCBI] 4.76786e-05
NGFB [NCBI] 2.75901e-05
MG [NCBI] 1.55101e-05



Database Center for Life Science