Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hyponatremia	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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