Abnormality of the autonomic nervous system

Symptom Information:

Symptom ID: HPO:0002270
Synonyms:
Autonomic nervous sytem anomaly [Orphanet:43010]
Dysautonomia [Orphanet:43010]
Autonomic nervous system disorders [Orphanet:43010]
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:0002271 "Autonomic dysregulation" [Orphanet:43010]
HPO:0002459 "Dysautonomia" [Orphanet:43010]
Orphanet:43010 "Dysautonomia/autonomous nervous sytem anomalies" [Orphanet:43010]
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: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         Abnormality of nervous system morphology
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)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neuromuscular disorders(MedDRA:10029317)
       Abnormality of the autonomic nervous system(HPO:0002270)
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

Alexander disease (Orphanet:58)
Atypical Rett syndrome (Orphanet:3095)
DYSAUTONOMIA-LIKE DISORDER (OMIM:224000)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Friedreich ataxia 1 (OMIM:229300)
Haddad syndrome (Orphanet:99803)
Hereditary sensory and autonomic neuropathy type 6 (Orphanet:314381)
Hereditary sensory and autonomic neuropathy with spastic paraplegia (Orphanet:139578)
METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASEA (OMIM:156310)
MUNGAN SYNDROME (OMIM:611376)
Melkersson-Rosenthal syndrome (Orphanet:2483)
Metachromatic leukodystrophy (Orphanet:512)
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome (Orphanet:329332)
NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUALPATHWAY AND AUTONOMIC DISTURBANCE (OMIM:162380)
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:605909)
RADICULONEUROPATHY, FATAL NEONATAL (OMIM:266250)
Rett syndrome (Orphanet:778)
Riboflavin transporter deficiency (Orphanet:97229)
Stüve-Wiedemann syndrome (Orphanet:3206)
Sudden infant death - dysgenesis of the testes (Orphanet:168593)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome, mitochondrial form (OMIM:598500)