Dyskinesia

Symptom Information:

Symptom ID: HPO:0100660
Synonyms:
DYSKINESIAS [HPO:0100660]
Dyskinesis [HPO:0100660]
Dyskinesia (finding) [Orphanet:43230]
Dyskinetic syndrome [Orphanet:43230]
Dyskinesia [OMIM:Dyskinesia]
Dyskinesias [OMIM:Dyskinesias]
Hyperkinesia/dyskinesia [Orphanet:43230]
Dyskinesia [Orphanet:43230]
Dyskinesia [MedDRA:10013916]
Abnormal involuntary movements [MedDRA:10013916]
Acute dyskinesia [MedDRA:10013916]
Body movements involuntary [MedDRA:10013916]
Dyskinesia acute [MedDRA:10013916]
Dyskinesia aggravated [MedDRA:10013916]
Dyskinesia buccoglossal [MedDRA:10013916]
Dyskinesia circumoral [MedDRA:10013916]
Dyskinesia NEC [MedDRA:10013916]
Dyskinesia syndrome [MedDRA:10013916]
Dyskinetic syndrome [MedDRA:10013916]
Head-face-neck syndrome [MedDRA:10013916]
Head-face-neck-syndrome [MedDRA:10013916]
Involuntary movement (NOS) [MedDRA:10013916]
Involuntary movement oral [MedDRA:10013916]
Involuntary movement oral (circumoral) [MedDRA:10013916]
Involuntary muscle movement [MedDRA:10013916]
Jerkiness [MedDRA:10013916]
Jerky movement NOS [MedDRA:10013916]
Mouth movement impaired [MedDRA:10013916]
Movements abnormal [MedDRA:10013916]
Movements involuntary [MedDRA:10013916]
Movements involuntary (NOS) [MedDRA:10013916]
Movements involuntary of limbs [MedDRA:10013916]
Movements involuntary of muscle [MedDRA:10013916]
Movements spastic involuntary [MedDRA:10013916]
Muscle movement involuntary [MedDRA:10013916]
Oral dyskinesia [MedDRA:10013916]
Orofacial dyskinesia [MedDRA:10013916]
Syndrome dyskinetic [MedDRA:10013916]
Syndrome head-face-neck [MedDRA:10013916]
Tongue protrusion spastic involun [MedDRA:10013916]
Tongue protrusion spastic involuntary [MedDRA:10013916]
Abnormal involuntary movements [OMIM:Abnormal involuntary movements]
Abnormal movements [OMIM:Abnormal movements]
Quality:
Cross references:
Orphanet:43230 "Hyperkinesia/dyskinesia" [Orphanet:43230]
OMIM: "Dyskinesia" [OMIM:Dyskinesia]
OMIM: "Dyskinesias" [OMIM:Dyskinesias]
OMIM: "Abnormal involuntary movements" [OMIM:Abnormal involuntary movements]
OMIM: "Abnormal movements" [OMIM:Abnormal movements]
UMLS:C0013384 "Dyskinetic syndrome" [Orphanet:43230]
Is a (Direct Parents):
HPO         Tardive dyskinesia
MedDRA Dyskinesias and movement disorders NEC
HPO         Abnormality of movement
Orphanet Abnormality of movement
Orphanet Hyperkinesis
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)
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)