Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   orthostatic hypotension
  

Disease ID 1942
Disease orthostatic hypotension
Definition
A significant drop in BLOOD PRESSURE after assuming a standing position. Orthostatic hypotension is a finding, and defined as a 20-mm Hg decrease in systolic pressure or a 10-mm Hg decrease in diastolic pressure 3 minutes after the person has risen from supine to standing. Symptoms generally include DIZZINESS, blurred vision, and SYNCOPE.
Synonym
hypotension orthostatic
hypotension postural
hypotension, orthostatic
hypotension, orthostatic [disease/finding]
hypotension, postural
orthostatic hypotension (disorder)
postural hypotension
ICD10
UMLS
C0020651
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:36)
C0030567  |  parkinson's disease  |  18
C0020538  |  hypertension  |  7
C0042373  |  vascular disease  |  4
C0030567  |  parkinson disease  |  3
C0242350  |  erectile dysfunction  |  2
C0018801  |  heart failure  |  2
C0007222  |  cardiovascular disease  |  2
C0011991  |  diarrhea  |  2
C0011570  |  depression  |  2
C0011847  |  diabetes  |  2
C0020255  |  hydrocephalus  |  1
C0022116  |  ischaemia  |  1
C0011854  |  type 1 diabetes  |  1
C0031511  |  pheochromocytoma  |  1
C0007682  |  central nervous system diseases  |  1
C0002395  |  alzheimer's disease  |  1
C0152025  |  polyneuropathy  |  1
C0027765  |  nervous system diseases  |  1
C0002726  |  amyloidosis  |  1
C0155616  |  secondary hypertension  |  1
C0442874  |  neuropathy  |  1
C0028738  |  nystagmus  |  1
C0011860  |  type 2 diabetes mellitus  |  1
C0497327  |  dementia  |  1
C0027051  |  myocardial infarct  |  1
C0007682  |  central nervous system disease  |  1
C0027051  |  myocardial infarction  |  1
C0393571  |  multiple system atrophy  |  1
C0027765  |  nervous system disease  |  1
C0242379  |  lung cancer  |  1
C0011860  |  type 2 diabetes  |  1
C0042870  |  vitamin d deficiency  |  1
C0023470  |  myeloid leukemia  |  1
C0023467  |  acute myeloid leukemia  |  1
C0002736  |  amyotrophic lateral sclerosis  |  1
C0042870  |  vitamin d defic  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:3)
5243  |  ABCB1  |  CTD_human
4988  |  OPRM1  |  CTD_human
4985  |  OPRD1  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:4)
2778  |  GNAS  |  CIPHER
5243  |  ABCB1  |  CTD_human
4988  |  OPRM1  |  CTD_human
4985  |  OPRD1  |  CTD_human
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1942
Disease orthostatic hypotension
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:41)
HP:0000822  |  Hypertension  |  9
HP:0001279  |  Syncope  |  8
HP:0002615  |  Low blood pressure  |  4
HP:0002315  |  Headaches  |  3
HP:0002527  |  Falls  |  3
HP:0002014  |  Diarrhea  |  2
HP:0007185  |  Loss of consciousness  |  2
HP:0000716  |  Depression  |  2
HP:0002459  |  Dysautonomia  |  2
HP:0000802  |  Erectile dysfunction  |  2
HP:0001635  |  Congestive heart failure  |  2
HP:0000622  |  Blurred vision  |  1
HP:0004808  |  Acute myelogenous leukemia  |  1
HP:0000975  |  Increased sweating  |  1
HP:0000238  |  Nonsyndromal hydrocephalus  |  1
HP:0003394  |  Muscle cramps  |  1
HP:0011034  |  Amyloid disease  |  1
HP:0007354  |  Amyotrophic lateral sclerosis  |  1
HP:0100512  |  Vitamin D deficiency  |  1
HP:0001751  |  Vestibular dysfunction  |  1
HP:0001278  |  Orthostatic hypotension  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0001649  |  Tachycardia  |  1
HP:0011675  |  Arrhythmias  |  1
HP:0002271  |  Autonomic dysregulation  |  1
HP:0012324  |  Myeloid leukemia  |  1
HP:0001658  |  Myocardial infarction  |  1
HP:0002140  |  Ischemic stroke  |  1
HP:0002172  |  Postural instability  |  1
HP:0002063  |  Muscle rigidity  |  1
HP:0002573  |  Bloody diarrhea  |  1
HP:0012173  |  Postural tachycardia  |  1
HP:0000726  |  Dementia  |  1
HP:0002666  |  Pheochromocytoma  |  1
HP:0001271  |  Polyneuropathy  |  1
HP:0002396  |  Cogwheel rigidity  |  1
HP:0011856  |  Pica  |  1
HP:0002157  |  Azotaemia  |  1
HP:0012594  |  High urine albumin levels  |  1
HP:0002321  |  Vertigo  |  1
HP:0000639  |  Nystagmus  |  1
Disease ID 1942
Disease orthostatic hypotension
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Disease ID 1942
Disease orthostatic hypotension
Case(Waiting for update.)