Gendoo

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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