Dysautonomia

Symptom Information:

Symptom ID: HPO:0002459
Synonyms:
Autonomic dysfunction [HPO:0002459]
Autonomic nervous sytem anomaly [Orphanet:43010]
Dysautonomia [Orphanet:43010]
Autonomic nervous system disorders [Orphanet:43010]
Autonomic dysfunction [OMIM:Autonomic dysfunction]
Dysautonomia [OMIM:Dysautonomia]
Dysautonomia/autonomous nervous sytem anomalies [Orphanet:43010]
Unspecified disorder of autonomic nervous system [Orphanet:43010]
Autonomic neuropathy [MedDRA:10061666]
Autonomic neuropathy NOS [MedDRA:10061666]
Disorders of the autonomic nervous system [MedDRA:10061666]
Idiopathic peripheral autonomic neuropathy [MedDRA:10061666]
Peripheral autonomic neuropathy in disorders classified elsewhere [MedDRA:10061666]
Unspecified disorder of autonomic nervous system [MedDRA:10061666]
Autonomic nervous system imbalance [MedDRA:10003840]
Autonomic imbalance [MedDRA:10003840]
Dysautonomia [MedDRA:10003840]
Imbalance autonomic nervous system [MedDRA:10003840]
Instability vasomotor [MedDRA:10003840]
Autonomic instability [MedDRA:10003840]
Autonomic dysfunction [MedDRA:10003840]
Autonomic vascular dystonia [MedDRA:10003840]
Psychovegetative syndrome [MedDRA:10003840]
Vegetative dystonia [MedDRA:10003840]
Neurovegetative neurosis [MedDRA:10003840]
Neurocirculatory dystonia [MedDRA:10003840]
Vasoneurosis [MedDRA:10003840]
Autonomic instability [OMIM:Autonomic instability]
Autonomic instability (22%) [OMIM:Autonomic instability (22%)]
Autonomic neuropathy [OMIM:Autonomic neuropathy]
Vasomotor instability [OMIM:Vasomotor instability]
Autonomic nervous system disorders [MedDRA:10003839]
Quality:
Cross references:
HPO:0002270 "Abnormality of the autonomic nervous system" [Orphanet:43010]
HPO:0002271 "Autonomic dysregulation" [Orphanet:43010]
Orphanet:43010 "Dysautonomia/autonomous nervous sytem anomalies" [Orphanet:43010]
OMIM: "Autonomic dysfunction" [OMIM:Autonomic dysfunction]
OMIM: "Dysautonomia" [OMIM:Dysautonomia]
OMIM: "Autonomic instability" [OMIM:Autonomic instability]
OMIM: "Autonomic instability (22%)" [OMIM:Autonomic instability (22%)]
OMIM: "Autonomic neuropathy" [OMIM:Autonomic neuropathy]
OMIM: "Vasomotor instability" [OMIM:Vasomotor instability]
UMLS:C0013363 "Dysautonomia" [HPO:0002459]
UMLS:C1145628 "Autonomic nervous system disorders" [Orphanet:43010]
UMLS:C0013363 "Dysautonomia" [Orphanet:43010]
Is a (Direct Parents):
MedDRA Neuromuscular disorders
Orphanet Functional anomalies of the nervous system
HPO         Abnormal autonomic nervous system physiology
MedDRA Abnormality of the autonomic nervous system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Abnormality of the autonomic nervous system(HPO:0002270)
                Abnormal autonomic nervous system physiology(HPO:0012332)
                   Dysautonomia(HPO:0002459)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neuromuscular disorders(MedDRA:10029317)
       Abnormality of the autonomic nervous system(HPO:0002270)
          Dysautonomia(HPO:0002459)
       Dysautonomia(HPO:0002459)
Database Frequency: 34 / 7739
Resource:

All diseases associated with this symptom:

ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME (OMIM:231550)
ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME (OMIM:615510)
ATTRV122I amyloidosis (Orphanet:85451)
Adult-onset autosomal dominant leukodystrophy (Orphanet:99027)
Autosomal dominant spastic paraplegia type 3 (Orphanet:100984)
Beta-propeller protein-associated neurodegeneration (Orphanet:329284)
DYSAUTONOMIA-LIKE DISORDER (OMIM:224000)
EPISODIC PAIN SYNDROME, FAMILIAL, 3 (OMIM:615552)
Fabry disease (Orphanet:324)
Familial amyloid polyneuropathy (Orphanet:85447)
Fatal familial insomnia (Orphanet:466)
HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION (OMIM:613870)
Hereditary sensory and autonomic neuropathy type 4 (Orphanet:642)
Hereditary sensory and autonomic neuropathy type 6 (Orphanet:314381)
METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASEA (OMIM:156310)
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome (Orphanet:329332)
Multiple system atrophy (Orphanet:102)
NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUALPATHWAY AND AUTONOMIC DISTURBANCE (OMIM:162380)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII (OMIM:615548)
PARKINSON DISEASE 4, AUTOSOMAL DOMINANT (OMIM:605543)
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:605909)
PARKINSON DISEASE, LATE-ONSET (OMIM:168600)
Peripheral motor neuropathy - dysautonomia (Orphanet:2400)
Pitt-Hopkins syndrome (Orphanet:2896)
RADICULONEUROPATHY, FATAL NEONATAL (OMIM:266250)
RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL (OMIM:614498)
Sodium channelopathy-related small fiber neuropathy (Orphanet:306577)
Spinocerebellar ataxia type 3 (Orphanet:98757)
Stüve-Wiedemann syndrome (Orphanet:3206)
Triple A syndrome (Orphanet:869)
Wilson disease (Orphanet:905)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome 1 (OMIM:222300)
Wolfram syndrome, mitochondrial form (OMIM:598500)