Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Vitreous Hemorrhage	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	0.000105673
VEGFA	[NCBI]	2.09828e-05
ARMS2	[NCBI]	1.18935e-05
SERPINF1	[NCBI]	8.56764e-06
VHL	[NCBI]	6.99602e-06
HGF	[NCBI]	5.54804e-06
GFAP	[NCBI]	5.07024e-06

OMIM	Link	Information gain
VRNI	[NCBI]	0.00491915
EVR1	[NCBI]	9.17009e-05
RB1	[NCBI]	8.37284e-05
galactosemia	[NCBI]	8.00136e-05
IP	[NCBI]	6.45852e-05
protein c deficiency, congenital thrombotic disease due to	[NCBI]	4.67974e-05
PLG	[NCBI]	3.88174e-05
PEDF	[NCBI]	3.8157e-05
VEGF	[NCBI]	3.77678e-05
thrombocytopenic purpura, autoimmune	[NCBI]	2.99441e-05
HGF	[NCBI]	1.60491e-05
GFAP	[NCBI]	1.28588e-05
SLE	[NCBI]	2.0854e-06