Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Wernicke Encephalopathy	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	5.28348e-05
TKT	[NCBI]	1.49174e-05
GFAP	[NCBI]	1.389e-05
APLP2	[NCBI]	1.24271e-05
APLP1	[NCBI]	1.15501e-05
MAPT	[NCBI]	7.89316e-06
APOE	[NCBI]	5.17188e-06

OMIM	Link	Information gain
wernicke-korsakoff syndrome	[NCBI]	0.00603512
alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus	[NCBI]	0.000133535
leigh syndrome, x-linked	[NCBI]	0.000128028
lactic acidosis, fatal infantile	[NCBI]	0.000115632
TKTL1	[NCBI]	9.19492e-05
CHAC	[NCBI]	8.99842e-05
TKT	[NCBI]	7.71931e-05
LS	[NCBI]	7.49402e-05
GFAP	[NCBI]	5.62884e-05
CJD	[NCBI]	3.52955e-05
APOE	[NCBI]	2.08784e-05