Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hypoaldosteronism	[NCBI]

Gene	Link	Information Gain
CYP11B2	[NCBI]	5.20569e-05
SLC4A4	[NCBI]	1.3485e-05
SCNN1B	[NCBI]	1.13948e-05
SLC12A3	[NCBI]	1.0857e-05
SLC9A3	[NCBI]	9.76586e-06
PTH	[NCBI]	4.31111e-06

OMIM	Link	Information gain
hyperreninemic hypoaldosteronism, familial, 2	[NCBI]	0.00159179
corticosterone methyloxidase type ii deficiency	[NCBI]	0.000354253
CYP11B2	[NCBI]	0.000136143
cortisol 11-beta-ketoreductase deficiency	[NCBI]	0.000110801
liddle syndrome	[NCBI]	9.63076e-05
PHA2	[NCBI]	8.77542e-05
SCNN1A	[NCBI]	6.724e-05
IL6	[NCBI]	4.17052e-05
ALD	[NCBI]	3.82965e-05
FMF	[NCBI]	3.22336e-05
PTH	[NCBI]	9.14044e-06
SLE	[NCBI]	1.36693e-08