MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Bartter Syndrome
[NCBI]
Gene
Gene
Link
Information
Gain
01
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
OMIM
Link
Information
gain
01
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
Database Center for Life Science