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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