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PedAM

Pediatric Disease Annotations & Medicines



   dysautonomia
  

Disease ID 1681
Disease dysautonomia
Definition
An acute or chronic disorder, affecting the sympathetic or parasympathetic nervous system. It can be primary, the result of central nervous system degeneration, or secondary due to diabetes or alcoholism. Patients with the chronic form of this disorder usually have a progressive clinical course and a poor prognosis.
Synonym
dysautonomia, nos
dysautonomia, primary
dysautonomias
dysautonomias, primary
primary dysautonomia
primary dysautonomias
primary dysautonomias [disease/finding]
UMLS
C0013363
MeSH
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:24)
C0030567  |  parkinson's disease  |  4
C0030567  |  parkinson disease  |  2
C1527336  |  sjogren's syndrome  |  2
C0393571  |  multiple system atrophy  |  2
C0011882  |  diabetic neuropathy  |  2
C0442874  |  neuropathy  |  2
C0026769  |  multiple sclerosis  |  2
C0011847  |  diabetes  |  1
C0206754  |  neuroendocrine tumors  |  1
C0025362  |  mental retardation  |  1
C0007785  |  cerebral ischemia  |  1
C0014544  |  epilepsy  |  1
C0270921  |  axonal neuropathy  |  1
C1096063  |  intractable epilepsy  |  1
C0020538  |  hypertension  |  1
C0042769  |  viral infection  |  1
C0206754  |  neuroendocrine tumor  |  1
C0878544  |  cardiomyopathy  |  1
C0002395  |  alzheimer's disease  |  1
C0020179  |  huntington's disease  |  1
C0004352  |  autism  |  1
C0022116  |  ischemia  |  1
C0025309  |  meningoencephalitis  |  1
C0011570  |  depression  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1681
Disease dysautonomia
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:29)
HP:0001276  |  Hypertonia  |  2
HP:0001649  |  Tachycardia  |  2
HP:0011703  |  Sinus tach  |  2
HP:0001278  |  Orthostatic hypotension  |  2
HP:0000716  |  Depression  |  1
HP:0001382  |  Hyperextensible joints  |  1
HP:0001249  |  Mental retardation  |  1
HP:0012879  |  Ejaculatory incompetence  |  1
HP:0002321  |  Vertigo  |  1
HP:0000822  |  Hypertension  |  1
HP:0002637  |  Brain ischemia  |  1
HP:0002789  |  Increased respiratory rate or depth of breathing  |  1
HP:0000717  |  Autism  |  1
HP:0001256  |  Mild mental retardation  |  1
HP:0003111  |  Electrolyte disorders  |  1
HP:0001638  |  Cardiomyopathy  |  1
HP:0011675  |  Arrhythmias  |  1
HP:0040182  |  Inappropriate sinus tachycardia  |  1
HP:0003470  |  Inability to move  |  1
HP:0000511  |  Vertical supranuclear gaze palsy  |  1
HP:0001773  |  Small feet  |  1
HP:0010819  |  drop attacks  |  1
HP:0000708  |  Behavioral problems  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0003477  |  Peripheral axonal neuropathy  |  1
HP:0001289  |  Confusion  |  1
HP:0000158  |  Abnormally large tongue  |  1
HP:0001695  |  Cardiac arrest  |  1
HP:0001250  |  Seizures  |  1
Disease ID 1681
Disease dysautonomia
Manually Symptom
UMLS  | Name(Total Manually Symptoms:5)
C1963093  |  dizziness
C0426768  |  o sign
C0270846  |  atonic seizures
C0029896  |  ent diseases
C0020649  |  hypotension
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:2)
C0270846  |  atonic seizures  |  1
C0012833  |  dizziness  |  1
Manually Genotype(Total Text Mining 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.)
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)