Dyskinesia
Symptom Information:
Symptom ID: | HPO:0100660 | |||||||||||||||||||||||||||||||||||||||||||
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 physiology(HPO:0012638) Abnormality of movement(HPO:0100022) Dyskinesia(HPO:0100660) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Dyskinesias and movement disorders NEC(MedDRA:10013929) Dyskinesia(HPO:0100660) |
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Database Frequency: | 19 / 7739 | |||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Arrhythmogenic right ventricular dysplasia, familial, 6 | (OMIM:604401) |
Autosomal recessive spastic paraplegia type 26 | (Orphanet:101006) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 | (OMIM:615483) |
Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
EPISODIC KINESIGENIC DYSKINESIA 1 | (OMIM:128200) |
EPISODIC KINESIGENIC DYSKINESIA 2 | (OMIM:611031) |
Early-onset parkinsonism - intellectual deficit | (Orphanet:2379) |
Familial dyskinesia and facial myokymia | (Orphanet:324588) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Hereditary folate malabsorption | (Orphanet:90045) |
Infantile dystonia-parkinsonism | (Orphanet:238455) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
PARKINSON DISEASE 17 | (OMIM:614203) |
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity | (Orphanet:53583) |
Paroxysmal exertion-induced dyskinesia | (Orphanet:98811) |
Pontine tegmental cap dysplasia | (Orphanet:269229) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
RETT SYNDROME, CONGENITAL VARIANT | (OMIM:613454) |
Tako-Tsubo cardiomyopathy | (Orphanet:66529) |