Abnormality of the autonomic nervous system
Symptom Information:
Symptom ID: | HPO:0002270 | |||||||||||||||||||||||||||||
Synonyms: |
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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) MedDRA: Nervous system disorders(MedDRA:10029205) Neuromuscular disorders(MedDRA:10029317) Abnormality of the autonomic nervous system(HPO:0002270) |
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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) |