Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Esotropia [NCBI]

Gene


 Gene Link Information
Gain		 01
KTWS [NCBI] 0.000332969
AAAS [NCBI] 1.18302e-05
FOXL2 [NCBI] 1.16617e-05
OCA2 [NCBI] 1.10934e-05
TYR [NCBI] 1.0297e-05
TYRP1 [NCBI] 1.00543e-05
PAX6 [NCBI] 8.70701e-06
FGFR3 [NCBI] 7.86924e-06
VEGFA [NCBI] 5.11512e-06



OMIM


 OMIM Link Information
gain		 01
blepharophimosis with ptosis, syndactyly, and short stature [NCBI] 0.00236515
arteriosclerosis, severe juvenile [NCBI] 0.00116675
HFH [NCBI] 0.000948879
strabismus, susceptibility to [NCBI] 0.000673834
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth [NCBI] 0.000673834
marden-walker syndrome [NCBI] 0.000561
dubowitz syndrome [NCBI] 0.000515156
CDG1A [NCBI] 0.000166755
radial ray hypoplasia with choanal atresia [NCBI] 0.000150059
oculopalatoskeletal syndrome [NCBI] 0.000113601
STL3 [NCBI] 0.000106243
polymicrogyria, bilateral frontoparietal [NCBI] 0.000106243
STL2 [NCBI] 0.00010353
STL1 [NCBI] 7.47252e-05
GCPS [NCBI] 7.2386e-05
BPES [NCBI] 6.88211e-05
NPS [NCBI] 6.54285e-05
WBS [NCBI] 4.83707e-05



Database Center for Life Science