Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hemosiderosis	[NCBI]

Gene	Link	Information Gain
DHS	[NCBI]	0.000362052
HFE	[NCBI]	7.68574e-05
CP	[NCBI]	1.68144e-05
BCS1L	[NCBI]	1.24139e-05
DMRT1	[NCBI]	1.08556e-05
HAMP	[NCBI]	9.65146e-06
EPO	[NCBI]	9.18373e-06
PANK2	[NCBI]	8.91217e-06
SERPINA1	[NCBI]	7.45354e-06
HLA-A	[NCBI]	6.45066e-06
HLA-B	[NCBI]	6.04001e-06
NOS3	[NCBI]	4.22105e-06
VWF	[NCBI]	3.48073e-06
MPO	[NCBI]	3.37511e-06

OMIM	Link	Information gain
DIP	[NCBI]	0.000817902
pseudohyperkalemia, familial, 1, due to red cell leak	[NCBI]	0.000798231
DHS	[NCBI]	0.000660154
iron overload in africa	[NCBI]	0.0004313
aceruloplasminemia	[NCBI]	0.000284693
pulmonary hemosiderosis	[NCBI]	0.000272372
gracile syndrome	[NCBI]	0.000187856
hemosiderosis, pulmonary, with deficiency of gamma-a globulin	[NCBI]	0.00013578
CP	[NCBI]	0.000123469
PVOD	[NCBI]	8.49166e-05
HFE	[NCBI]	7.5046e-05
crigler-najjar syndrome	[NCBI]	6.7806e-05
BCS1L	[NCBI]	6.30871e-05
PANK2	[NCBI]	5.21719e-05
anemia, sideroblastic, x-linked	[NCBI]	4.71057e-05
ZS	[NCBI]	4.24633e-05
KSS	[NCBI]	3.86308e-05
LAM	[NCBI]	3.54922e-05
GHRH	[NCBI]	2.95574e-05
EPO	[NCBI]	2.89941e-05
PI	[NCBI]	2.78364e-05
RA	[NCBI]	2.0374e-05
thrombocytopenic purpura, autoimmune	[NCBI]	8.89426e-06
MPO	[NCBI]	8.20034e-06
CF	[NCBI]	1.32264e-06