Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Uvea	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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