Athetosis

Symptom Information:

Symptom ID: HPO:0002305
Synonyms:
Athetoid movements [HPO:0002305]
Athetosis (disorder) [Orphanet:43250]
Athetoid movement (finding) [Orphanet:43250]
Athetoid [Orphanet:43250]
Athetosis [Orphanet:43250]
Athetoid movements [OMIM:Athetoid movements]
Athetosis [OMIM:Athetosis]
Chorea/athetosis/choreoathetosis/choreic syndrome [Orphanet:43250]
Athetosis [MedDRA:10003620]
Athetoid [MedDRA:10003620]
Athetosis (in some patients) [OMIM:Athetosis (in some patients)]
Athetosis (later) [OMIM:Athetosis (later)]
Quality:
Cross references:
Orphanet:43250 "Chorea/athetosis/choreoathetosis/choreic syndrome" [Orphanet:43250]
OMIM: "Athetoid movements" [OMIM:Athetoid movements]
OMIM: "Athetosis" [OMIM:Athetosis]
OMIM: "Athetosis (in some patients)" [OMIM:Athetosis (in some patients)]
OMIM: "Athetosis (later)" [OMIM:Athetosis (later)]
UMLS:C0004158 "Athetosis" [HPO:0002305]
UMLS:C0541790 "Athetoid" [Orphanet:43250]
UMLS:C0004158 "Athetosis" [Orphanet:43250]
Is a (Direct Parents):
MedDRA Chorea
HPO         Involuntary movements
Orphanet Choreoathetosis
Orphanet Abnormality of movement
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Involuntary movements(HPO:0004305)
                Athetosis(HPO:0002305)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of movement(HPO:0100022)
                Involuntary movements(HPO:0004305)
                   Athetosis(HPO:0002305)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Chorea(HPO:0002072)
          Athetosis(HPO:0002305)
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 1 (Orphanet:67046)
ALDH18A1-related De Barsy syndrome (Orphanet:35664)
AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA (OMIM:300857)
Aceruloplasminemia (Orphanet:48818)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Alpers syndrome (Orphanet:726)
Autosomal recessive limb-girdle muscular dystrophy type 2S (Orphanet:369840)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 (OMIM:213600)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 (OMIM:615483)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
Cystic leukoencephalopathy without megalencephaly (Orphanet:85136)
De Barsy syndrome (Orphanet:2962)
ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD (OMIM:130950)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17 (OMIM:615473)
Gaucher disease type 2 (Orphanet:77260)
Hereditary folate malabsorption (Orphanet:90045)
Infantile cerebellar-retinal degeneration (Orphanet:313850)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
LEBER OPTIC ATROPHY AND DYSTONIA (OMIM:500001)
Leigh syndrome (Orphanet:506)
MICROHYDRANENCEPHALY (OMIM:605013)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4 (OMIM:615159)
Menkes disease (Orphanet:565)
Methylmalonic acidemia with homocystinuria, type cblX (Orphanet:369962)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Niemann-Pick disease type A (Orphanet:77292)
Niemann-Pick disease type C (Orphanet:646)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
RETT SYNDROME, CONGENITAL VARIANT (OMIM:613454)
Salla disease (Orphanet:309334)