Dysautonomia
Symptom Information:
Symptom ID: | HPO:0002459 | ||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |