Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Retinal Perforations	[NCBI]

Gene	Link	Information Gain
VEGFA	[NCBI]	0.00013698
SERPINF1	[NCBI]	4.16267e-05
COL2A1	[NCBI]	3.5733e-05
TGFB2	[NCBI]	3.40896e-05
GFAP	[NCBI]	2.41097e-05
PDE6B	[NCBI]	8.52654e-06
RLBP1	[NCBI]	8.32283e-06
IL6R	[NCBI]	7.80271e-06
MME	[NCBI]	7.73336e-06
HMGB1	[NCBI]	7.50081e-06
ABCA4	[NCBI]	6.55569e-06
ANGPT1	[NCBI]	6.55569e-06
ADM	[NCBI]	5.76609e-06
PGF	[NCBI]	5.26803e-06
CTGF	[NCBI]	4.19343e-06
VIP	[NCBI]	3.46281e-06
IL6	[NCBI]	2.96086e-06
TNFSF10	[NCBI]	2.89587e-06
CD68	[NCBI]	2.83362e-06
HGF	[NCBI]	2.5795e-06
TGFB1	[NCBI]	2.23598e-06
FASLG	[NCBI]	2.09824e-06

OMIM	Link	Information gain
VRNI	[NCBI]	0.0277183
MYP2	[NCBI]	0.000644738
RP	[NCBI]	0.000182778
RS1	[NCBI]	0.000159308
VEGF	[NCBI]	0.000122133
stickler syndrome, type i, nonsyndromic ocular	[NCBI]	0.000116574
GFAP	[NCBI]	9.42403e-05
panencephalitis, subacute sclerosing	[NCBI]	4.03173e-05
COL2A1	[NCBI]	3.47044e-05
PEDF	[NCBI]	2.78292e-05
ADM	[NCBI]	2.75809e-05
CTGF	[NCBI]	1.98882e-05
TNFSF6	[NCBI]	1.12974e-05
VIP	[NCBI]	1.09275e-05
HGF	[NCBI]	7.0448e-06