MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Hypotension, Orthostatic
[NCBI]
Gene
Gene
Link
Information
Gain
01
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
OMIM
Link
Information
gain
01
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
Database Center for Life Science