Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hypotension, Orthostatic	[NCBI]

Gene	Link	Information Gain
OHDS	[NCBI]	0.000373825
MS	[NCBI]	0.000206848
AVP	[NCBI]	9.01833e-05
DBH	[NCBI]	3.70361e-05
NEDD4L	[NCBI]	2.45127e-05
SNCA	[NCBI]	2.43252e-05
SLC6A2	[NCBI]	1.70671e-05
NPY	[NCBI]	1.39427e-05
AGTR1	[NCBI]	1.32047e-05
EPO	[NCBI]	1.20217e-05
PLEKHG4	[NCBI]	1.07193e-05
ECE1	[NCBI]	1.02108e-05
ADRA2B	[NCBI]	9.8192e-06
ADRA2C	[NCBI]	9.75058e-06
ADRA2A	[NCBI]	8.91556e-06
ADRB1	[NCBI]	7.35144e-06
NPPA	[NCBI]	7.12029e-06
GNB3	[NCBI]	6.6135e-06
EDN1	[NCBI]	6.21564e-06
PRL	[NCBI]	6.19795e-06
GNAS	[NCBI]	6.16576e-06
ADRB2	[NCBI]	5.43397e-06
PRKCB	[NCBI]	5.17034e-06
IGF1	[NCBI]	4.82904e-06
ABCB1	[NCBI]	4.63219e-06
AGT	[NCBI]	4.47122e-06
PARK2	[NCBI]	4.31405e-06
ACE	[NCBI]	3.4283e-06
TH	[NCBI]	3.16762e-06

OMIM	Link	Information gain
orthostatic hypotensive disorder, streeten type	[NCBI]	0.00115589
PARK3	[NCBI]	0.000862873
dopamine beta-hydroxylase deficiency, congenital	[NCBI]	0.000584448
AVP	[NCBI]	0.000375125
hypotension, orthostatic	[NCBI]	0.00033761
PD	[NCBI]	0.000145698
neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia	[NCBI]	0.000137445
NPPA	[NCBI]	0.000123154
orthostatic intolerance	[NCBI]	9.36381e-05
amyloidosis v	[NCBI]	7.48942e-05
NEDD4L	[NCBI]	7.10704e-05
AIMAH	[NCBI]	6.13656e-05
DBH	[NCBI]	5.15571e-05
wilson disease	[NCBI]	4.53241e-05
fabry disease	[NCBI]	4.42173e-05
NPY	[NCBI]	4.21181e-05
EPO	[NCBI]	3.23181e-05
FTD	[NCBI]	1.93554e-05
FMF	[NCBI]	1.88505e-05
PRL	[NCBI]	1.18703e-05
TH	[NCBI]	6.24868e-06