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01 Pseudohypoaldosteronism [NCBI]

Gene


 Gene Link Information
Gain		 01
WNK4 [NCBI] 0.000246366
WNK1 [NCBI] 0.00024557
VUR [NCBI] 0.000189637
NR3C2 [NCBI] 0.000143869
SCNN1B [NCBI] 0.000118442
SCNN1A [NCBI] 0.000103029
KCNJ1 [NCBI] 4.45737e-05
SCNN1G [NCBI] 3.3652e-05
WNK3 [NCBI] 2.81435e-05
SLC12A3 [NCBI] 2.70631e-05
SGK1 [NCBI] 1.57829e-05
TESC [NCBI] 1.31586e-05
WNK2 [NCBI] 1.15084e-05
AQP1 [NCBI] 7.92495e-06
GNAS [NCBI] 5.58337e-06
TJP1 [NCBI] 5.13555e-06
CFTR [NCBI] 4.6059e-06
AKT1 [NCBI] 2.16184e-06



OMIM


 OMIM Link Information
gain		 01
hypertension, essential, susceptibility to, 1 [NCBI] 0.00123814
NR3C2 [NCBI] 0.00116585
PHA1 [NCBI] 0.000906535
pseudohypoaldosteronism, type i, autosomal dominant [NCBI] 0.000679094
PHA2 [NCBI] 0.000619433
WNK4 [NCBI] 0.000423458
SCNN1A [NCBI] 0.000190863
WNK1 [NCBI] 0.000190863
SCNN1B [NCBI] 0.000174845
SCNN1G [NCBI] 0.000125778
liddle syndrome [NCBI] 7.85178e-05
cortisol 11-beta-ketoreductase deficiency [NCBI] 7.75502e-05
c syndrome [NCBI] 7.47703e-05
bartter syndrome, antenatal, type 2 [NCBI] 7.36928e-05
dent disease 1 [NCBI] 7.36928e-05
bartter syndrome, type 3 [NCBI] 6.22591e-05
GRA [NCBI] 5.12757e-05
hypertension, essential [NCBI] 5.07731e-05
AHO [NCBI] 4.38862e-05
AQP1 [NCBI] 3.84781e-05
NPPA [NCBI] 8.19876e-06
CF [NCBI] 2.53484e-06



Database Center for Life Science