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01 Hypokalemia [NCBI]

Gene


 Gene Link Information
Gain		 01
SLC12A3 [NCBI] 0.000308935
SCNN1B [NCBI] 9.73624e-05
SLC12A1 [NCBI] 6.90299e-05
CLCNKB [NCBI] 6.30283e-05
KCNJ1 [NCBI] 5.38938e-05
VIP [NCBI] 4.67241e-05
CACNA1S [NCBI] 4.10333e-05
HSD11B2 [NCBI] 3.39693e-05
BSND [NCBI] 3.15408e-05
SCNN1G [NCBI] 3.13166e-05
CYP17A1 [NCBI] 2.88195e-05
KCNQ1 [NCBI] 1.83207e-05
HSD11B1 [NCBI] 1.54894e-05
SLC26A7 [NCBI] 1.23906e-05
SCN5A [NCBI] 1.1469e-05
GIP [NCBI] 1.11893e-05
ATP6V1B1 [NCBI] 9.48558e-06
CLCNKA [NCBI] 8.85505e-06
PTGES [NCBI] 8.20497e-06
CYP11B1 [NCBI] 7.98017e-06
WNK1 [NCBI] 7.29568e-06
KCNE1 [NCBI] 6.54072e-06
SCN4A [NCBI] 6.1588e-06
SGK1 [NCBI] 5.92418e-06
KCNJ8 [NCBI] 5.83287e-06
CYP11B2 [NCBI] 5.59832e-06
MB [NCBI] 5.59832e-06
KCNH2 [NCBI] 5.57277e-06
PTGES2 [NCBI] 4.95527e-06
KCNH6 [NCBI] 4.44207e-06
ERG [NCBI] 4.41675e-06
AMBP [NCBI] 4.2385e-06
ADRB2 [NCBI] 4.10887e-06
AGTR1 [NCBI] 4.07804e-06
MEN1 [NCBI] 3.75243e-06
CYP3A4 [NCBI] 3.63661e-06
CTSL1 [NCBI] 3.35888e-06
CFTR [NCBI] 3.26813e-06
TROVE2 [NCBI] 3.25923e-06
PTH [NCBI] 2.57179e-06
AVP [NCBI] 1.86863e-06
NOS3 [NCBI] 1.77246e-06
PTGS2 [NCBI] 4.58706e-07



OMIM


 OMIM Link Information
gain		 01
hypokalemia, familial [NCBI] 0.00510184
HOKPP [NCBI] 0.00145049
cortisol 11-beta-ketoreductase deficiency [NCBI] 0.00089127
bartter syndrome, type 3 [NCBI] 0.000839252
gitelman syndrome [NCBI] 0.000822585
oculocerebral syndrome with hypopigmentation [NCBI] 0.000724991
liddle syndrome [NCBI] 0.000445618
CACNA1S [NCBI] 0.000367457
SLC12A3 [NCBI] 0.000358099
thyrotoxic periodic paralysis [NCBI] 0.000326016
bartter syndrome, infantile, with sensorineural deafness [NCBI] 0.000253123
bartter syndrome, antenatal, type 2 [NCBI] 0.000220912
VIP [NCBI] 0.000169421
GRA [NCBI] 0.00015117
CYP17A1 [NCBI] 0.000131457
diarrhea 1, secretory chloride, congenital [NCBI] 0.000125223
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency [NCBI] 0.000125223
CLCNKB [NCBI] 0.000113621
andersen cardiodysrhythmic periodic paralysis [NCBI] 0.000112761
GCCR [NCBI] 7.97459e-05
AME2 [NCBI] 7.8657e-05
bartter syndrome, antenatal, type 1 [NCBI] 7.13236e-05
HOMG [NCBI] 5.80901e-05
HOMG3 [NCBI] 5.68552e-05
CLCNKA [NCBI] 5.51838e-05
KCNH2 [NCBI] 5.50805e-05
lipoid congenital adrenal hyperplasia [NCBI] 5.46414e-05
dent disease 1 [NCBI] 5.46414e-05
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency [NCBI] 5.0972e-05
SCNN1G [NCBI] 4.90181e-05
PMC [NCBI] 4.86917e-05
diabetes insipidus, nephrogenic, x-linked [NCBI] 4.49391e-05
NPHP1 [NCBI] 4.43933e-05
CCAL2 [NCBI] 4.43933e-05
SCNN1B [NCBI] 4.04075e-05
GIP [NCBI] 3.95348e-05
AIMAH [NCBI] 3.9402e-05
CYP11B1 [NCBI] 3.81409e-05
HYPP [NCBI] 3.79283e-05
AVP [NCBI] 3.63892e-05
SCN4A [NCBI] 3.12039e-05
LQT1 [NCBI] 3.10336e-05
KCNQ1 [NCBI] 2.86152e-05
SLC4A1 [NCBI] 2.73766e-05
MB [NCBI] 2.03658e-05
KSS [NCBI] 1.94e-05
DMD [NCBI] 1.66643e-05
CRH [NCBI] 1.02433e-05
CVID [NCBI] 8.81839e-06
polycystic kidneys [NCBI] 7.53311e-06
AD [NCBI] 4.94954e-06
CF [NCBI] 2.97667e-06
CD [NCBI] 2.30627e-06
PTH [NCBI] 1.29623e-06



Database Center for Life Science