Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Metal Metabolism, Inborn Errors	[NCBI]

Gene	Link	Information Gain
CP	[NCBI]	2.87132e-05
HFE	[NCBI]	2.02501e-05
ATP7A	[NCBI]	1.90936e-05
SUOX	[NCBI]	1.35427e-05
FXYD2	[NCBI]	1.33275e-05
COMMD1	[NCBI]	1.22954e-05
ATOX1	[NCBI]	1.19012e-05
SLC40A1	[NCBI]	1.0485e-05
ATP7B	[NCBI]	8.90978e-06
TFR2	[NCBI]	8.83461e-06
CYP27A1	[NCBI]	8.40735e-06
FXN	[NCBI]	7.4247e-06
SLC11A1	[NCBI]	7.11378e-06
NOS2	[NCBI]	4.39235e-06

OMIM	Link	Information gain
zinc, elevated plasma	[NCBI]	0.00213636
HHC2	[NCBI]	0.000991404
menkes disease	[NCBI]	0.000479668
aceruloplasminemia	[NCBI]	0.000176359
COMMD1	[NCBI]	0.000161558
copper deficiency, familial benign	[NCBI]	0.000136591
wilson disease	[NCBI]	0.00011205
HOMG2	[NCBI]	9.27854e-05
ATP6V0E1	[NCBI]	8.31009e-05
SUOX	[NCBI]	8.31009e-05
CP	[NCBI]	8.14232e-05
HOMG	[NCBI]	7.9483e-05
hemochromatosis, neonatal	[NCBI]	7.82382e-05
molybdenum cofactor deficiency	[NCBI]	7.60048e-05
cutis laxa, autosomal recessive, type i	[NCBI]	7.14886e-05
cutis laxa, x-linked	[NCBI]	6.86125e-05
CACNA1C	[NCBI]	6.56767e-05
HEPH	[NCBI]	6.26709e-05
FIH	[NCBI]	6.21912e-05
HHC1	[NCBI]	6.01273e-05
NPC1	[NCBI]	5.33135e-05
NPC1	[NCBI]	5.07564e-05