Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hexosephosphates	[NCBI]

Gene	Link	Information Gain
MPO	[NCBI]	6.5164e-06
NAGPA	[NCBI]	4.50011e-06
HK1	[NCBI]	4.30452e-06
G6PD	[NCBI]	2.59359e-06
CTSL1	[NCBI]	2.54565e-06
FPGT	[NCBI]	2.464e-06
LGTN	[NCBI]	2.34953e-06
ALDOC	[NCBI]	2.26963e-06
H6PD	[NCBI]	2.15827e-06
PRPS1	[NCBI]	2.15827e-06
MPI	[NCBI]	2.07988e-06
PGD	[NCBI]	2.07988e-06
M6PR	[NCBI]	2.03323e-06
GCKR	[NCBI]	1.97569e-06
HEXB	[NCBI]	1.86437e-06
GALT	[NCBI]	1.81592e-06
REN	[NCBI]	1.67995e-06
MAN1C1	[NCBI]	1.65629e-06
GCK	[NCBI]	1.64941e-06
TF	[NCBI]	1.14771e-06
ACP5	[NCBI]	1.12999e-06
TG	[NCBI]	1.05924e-06
EGF	[NCBI]	5.19074e-07

OMIM	Link	Information gain
mannose 6-phosphate receptor recognition defect, lebanese type	[NCBI]	0.00277021
galactosemia	[NCBI]	0.000431387
mucolipidosis ii	[NCBI]	0.00031018
CGD	[NCBI]	0.000171615
IGF2R	[NCBI]	0.000129792
PHA	[NCBI]	0.000111755
myeloperoxidase deficiency	[NCBI]	0.000106042
glycogen storage disease ib	[NCBI]	9.16146e-05
GPX1	[NCBI]	9.01516e-05
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i	[NCBI]	8.99052e-05
LAD	[NCBI]	7.90344e-05
pyruvate kinase deficiency of red cells	[NCBI]	7.70959e-05
GPI	[NCBI]	7.62574e-05
G6PD	[NCBI]	6.70306e-05
WBS	[NCBI]	6.28782e-05
GALT	[NCBI]	5.04972e-05
FPGT	[NCBI]	4.81542e-05
MPO	[NCBI]	4.60794e-05
PKM2	[NCBI]	2.92835e-05
MPI	[NCBI]	2.77988e-05
ALDOA	[NCBI]	2.74843e-05
HK1	[NCBI]	2.54731e-05
fructose intolerance, hereditary	[NCBI]	2.26247e-05
GSR	[NCBI]	2.17259e-05
CTSL	[NCBI]	2.1328e-05
ITGB2	[NCBI]	2.1328e-05
IGF2	[NCBI]	2.07822e-05
H6PD	[NCBI]	1.87325e-05
SLE	[NCBI]	1.1331e-05
TF	[NCBI]	6.7852e-06
TG	[NCBI]	4.93208e-06
EGF	[NCBI]	3.81021e-07