Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Bartter Syndrome	[NCBI]

Gene	Link	Information Gain
CLCNKB	[NCBI]	0.000424062
KCNJ1	[NCBI]	0.000332288
SLC12A3	[NCBI]	0.000254563
BSND	[NCBI]	0.000236021
CLCNKA	[NCBI]	0.000160579
SLC12A1	[NCBI]	0.000125087
UMOD	[NCBI]	2.91659e-05
CASR	[NCBI]	2.8568e-05
RGS2	[NCBI]	1.7854e-05
CLCN1	[NCBI]	1.41737e-05
KCNJ13	[NCBI]	1.13634e-05
KCNJ15	[NCBI]	1.05842e-05
NOS3	[NCBI]	9.24219e-06
SLC12A6	[NCBI]	8.91976e-06
PTGS2	[NCBI]	7.63695e-06
ALS2	[NCBI]	7.29338e-06
AQP1	[NCBI]	6.71919e-06
SLC22A12	[NCBI]	6.62449e-06
SCNN1B	[NCBI]	6.4222e-06
SOX10	[NCBI]	6.10084e-06
INPP5D	[NCBI]	5.92983e-06
PTGER1	[NCBI]	5.56593e-06
SLC9A3	[NCBI]	4.81589e-06
AQP2	[NCBI]	4.51319e-06
PTH	[NCBI]	4.47551e-06
SHC1	[NCBI]	4.42908e-06
CYBA	[NCBI]	4.22888e-06

OMIM	Link	Information gain
bartter syndrome, type 3	[NCBI]	0.00230734
hypokalemia, familial	[NCBI]	0.00222949
bartter syndrome, antenatal, type 2	[NCBI]	0.00148715
oculocerebral syndrome with hypopigmentation	[NCBI]	0.000817902
bartter syndrome, infantile, with sensorineural deafness	[NCBI]	0.000782822
bartter syndrome, antenatal, type 1	[NCBI]	0.000736129
KCNJ1	[NCBI]	0.000667325
CLCNKB	[NCBI]	0.000582819
SLC12A3	[NCBI]	0.000468348
gitelman syndrome	[NCBI]	0.000372507
bsnd gene	[NCBI]	0.000306377
SLC12A1	[NCBI]	0.000225647
CLCNKA	[NCBI]	0.000225647
CASR	[NCBI]	0.000108327
KCNJ13	[NCBI]	8.23896e-05
NSHPT	[NCBI]	6.47746e-05
HOMG	[NCBI]	6.47746e-05
andersen cardiodysrhythmic periodic paralysis	[NCBI]	5.15507e-05
CCAL2	[NCBI]	5.10004e-05
KCNJ2	[NCBI]	4.66106e-05
HHC1	[NCBI]	4.55722e-05
AQP1	[NCBI]	3.73334e-05
KSS	[NCBI]	2.54461e-05
CF	[NCBI]	2.13417e-05
PTH	[NCBI]	1.38162e-05
AVP	[NCBI]	2.56346e-06