Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Uvea [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 8.69867e-05
NPY [NCBI] 1.30801e-05
TYRP1 [NCBI] 1.12596e-05
MYOC [NCBI] 1.10333e-05
DCT [NCBI] 1.0195e-05
FOXL2 [NCBI] 6.39673e-06
KITLG [NCBI] 5.74432e-06
TYR [NCBI] 5.61002e-06
LY96 [NCBI] 5.23838e-06
SOX2 [NCBI] 5.1891e-06
ATXN1 [NCBI] 4.96274e-06
KIT [NCBI] 4.87881e-06
NOD2 [NCBI] 4.54803e-06
SERPINF1 [NCBI] 4.28081e-06
MMP2 [NCBI] 4.15907e-06
CIITA [NCBI] 4.10685e-06
MMP9 [NCBI] 4.02907e-06
IRF1 [NCBI] 4.01212e-06
IFNGR1 [NCBI] 3.69657e-06
STAT1 [NCBI] 2.96976e-06
TLR4 [NCBI] 2.84886e-06
CCK [NCBI] 2.19748e-06
ACHE [NCBI] 2.03704e-06
TH [NCBI] 1.95318e-06
TNF [NCBI] 1.13108e-06




OMIM


OMIM Link Information
gain
01
MACOM [NCBI] 0.00145218
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth [NCBI] 0.0012742
marden-walker syndrome [NCBI] 0.00112909
dubowitz syndrome [NCBI] 0.00105678
coloboma, uveal, with cleft lip and palate and mental retardation [NCBI] 0.000536184
oculopalatoskeletal syndrome [NCBI] 0.00020079
TCOF [NCBI] 0.000130041
BPES [NCBI] 0.000125737
CHS [NCBI] 9.0478e-05
NPY [NCBI] 5.97911e-05
PTGS2 [NCBI] 3.17771e-05
TLR4 [NCBI] 1.93852e-05
VEGF [NCBI] 1.15697e-05
CCK [NCBI] 7.24818e-06
ACHE [NCBI] 6.26354e-06
TH [NCBI] 5.70598e-06
TNF [NCBI] 1.67385e-06




Database Center for Life Science