Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Alkalosis	[NCBI]

Gene	Link	Information Gain
SLC12A3	[NCBI]	0.000259544
CLCNKB	[NCBI]	4.29078e-05
SCNN1B	[NCBI]	4.11176e-05
SLC9A3	[NCBI]	3.45029e-05
KCNJ1	[NCBI]	3.23924e-05
PTH	[NCBI]	2.33984e-05
SLC12A1	[NCBI]	1.71419e-05
MINPP1	[NCBI]	1.33444e-05
TRPC4	[NCBI]	1.2761e-05
F2RL2	[NCBI]	1.14481e-05
SLC16A4	[NCBI]	1.03158e-05
BSND	[NCBI]	9.48745e-06
CFTR	[NCBI]	9.38606e-06
KCNK2	[NCBI]	9.15669e-06
SLC26A3	[NCBI]	8.78026e-06
SLC9A1	[NCBI]	8.21087e-06
AVP	[NCBI]	7.70858e-06
KCNJ8	[NCBI]	6.77773e-06
CLN3	[NCBI]	6.59444e-06
ALB	[NCBI]	4.65382e-06
TROVE2	[NCBI]	4.17044e-06
SOD1	[NCBI]	2.97079e-06
NOS3	[NCBI]	2.61471e-06

OMIM	Link	Information gain
hypokalemia, familial	[NCBI]	0.00252968
bartter syndrome, type 3	[NCBI]	0.000901283
gitelman syndrome	[NCBI]	0.0002923
cortisol 11-beta-ketoreductase deficiency	[NCBI]	0.000205996
SLC12A3	[NCBI]	0.000188732
CF	[NCBI]	0.000159749
diarrhea 1, secretory chloride, congenital	[NCBI]	0.000158546
PTH	[NCBI]	9.87716e-05
bartter syndrome, infantile, with sensorineural deafness	[NCBI]	8.07631e-05
liddle syndrome	[NCBI]	7.58729e-05
bartter syndrome, antenatal, type 2	[NCBI]	7.10508e-05
dent disease 1	[NCBI]	7.10508e-05
diabetes insipidus, nephrogenic, x-linked	[NCBI]	6.12371e-05
CLCNKB	[NCBI]	6.00921e-05
AVP	[NCBI]	4.98019e-05
GCCR	[NCBI]	4.38175e-05
ALB	[NCBI]	2.02896e-05
SLE	[NCBI]	1.90061e-05
CRH	[NCBI]	8.24088e-06
MG	[NCBI]	3.7199e-06