Autonomic dysregulation
Symptom Information:
Symptom ID: | HPO:0002271 | ||||||||||||||||||||||||||||||
Synonyms: |
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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) Autonomic dysregulation(HPO:0002271) MedDRA: Nervous system disorders(MedDRA:10029205) Neuromuscular disorders(MedDRA:10029317) Abnormality of the autonomic nervous system(HPO:0002270) Autonomic dysregulation(HPO:0002271) Autonomic dysregulation(HPO:0002271) |
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Database Frequency: | 11 / 7739 | ||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
DYSAUTONOMIA-LIKE DISORDER | (OMIM:224000) |
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) |
NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUALPATHWAY AND AUTONOMIC DISTURBANCE | (OMIM:162380) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:605909) |
RADICULONEUROPATHY, FATAL NEONATAL | (OMIM:266250) |
Waardenburg-Shah syndrome | (Orphanet:897) |
Wolfram syndrome | (Orphanet:3463) |
Wolfram syndrome, mitochondrial form | (OMIM:598500) |