MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Hyponatremia
[NCBI]
Gene
Gene
Link
Information
Gain
01
AVP
[NCBI]
0.000811129
AQP2
[NCBI]
0.000107362
MS
[NCBI]
0.000105673
AVPR2
[NCBI]
2.6362e-05
HCRTR1
[NCBI]
2.20227e-05
AQP4
[NCBI]
1.38707e-05
MC2R
[NCBI]
8.87931e-06
HCRTR2
[NCBI]
8.77215e-06
HCRT
[NCBI]
8.67131e-06
KCNJ1
[NCBI]
7.50952e-06
SLC26A3
[NCBI]
7.46068e-06
AAAS
[NCBI]
6.92785e-06
NR0B1
[NCBI]
6.72894e-06
PRL
[NCBI]
6.46198e-06
SLC12A1
[NCBI]
6.04417e-06
CDC25C
[NCBI]
5.40996e-06
NPPB
[NCBI]
5.11067e-06
CYP21A2
[NCBI]
5.08703e-06
CRH
[NCBI]
4.94112e-06
CYP2D6
[NCBI]
4.61138e-06
GDNF
[NCBI]
3.70761e-06
CYP3A4
[NCBI]
3.28574e-06
UMOD
[NCBI]
3.1899e-06
CHEK1
[NCBI]
2.99578e-06
CFTR
[NCBI]
2.66396e-06
TRH
[NCBI]
1.91534e-06
ACE
[NCBI]
1.85744e-06
OMIM
OMIM
Link
Information
gain
01
AVP
[NCBI]
0.00635135
corticosterone methyloxidase type ii deficiency
[NCBI]
0.000532492
PHA1
[NCBI]
0.00016411
corticosterone methyloxidase type i deficiency
[NCBI]
0.000131618
NSIAD
[NCBI]
9.51693e-05
AQP2
[NCBI]
8.97153e-05
SLOS
[NCBI]
8.00422e-05
GCCD1
[NCBI]
7.58729e-05
lipoid congenital adrenal hyperplasia
[NCBI]
7.10508e-05
bartter syndrome, antenatal, type 2
[NCBI]
7.10508e-05
CYP11B2
[NCBI]
6.97687e-05
PHA2
[NCBI]
6.73472e-05
diarrhea 1, secretory chloride, congenital
[NCBI]
6.73472e-05
hyperglycerolemia
[NCBI]
6.18115e-05
AVPR2
[NCBI]
5.89489e-05
ARPKD
[NCBI]
4.91858e-05
NPPA
[NCBI]
3.96239e-05
MC2R
[NCBI]
3.21607e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
[NCBI]
2.50592e-05
AQP4
[NCBI]
2.26034e-05
polycystic kidneys
[NCBI]
2.07833e-05
LIPC
[NCBI]
1.81827e-05
CF
[NCBI]
1.51399e-05
RA
[NCBI]
1.3827e-05
PTHLH
[NCBI]
1.14145e-06
GDNF
[NCBI]
1.04808e-06
CFTR
[NCBI]
3.81741e-07
SLE
[NCBI]
1.76805e-07
PRL
[NCBI]
5.89659e-08
Database Center for Life Science