Chorea

Symptom Information:

Symptom ID: HPO:0002072
Synonyms:
Choreatic disease [HPO:0002072]
Choreic movements [HPO:0002072]
Choreiform movements [HPO:0002072]
Chorea (finding) [Orphanet:43250]
Chorea [Orphanet:43250]
Chorea [OMIM:Chorea]
Choreic movements [OMIM:Choreic movements]
Choreiform movements [OMIM:Choreiform movements]
Chorea/athetosis/choreoathetosis/choreic syndrome [Orphanet:43250]
Chorea [MedDRA:10008748]
Chorea aggravated [MedDRA:10008748]
Chorea NOS [MedDRA:10008748]
Choreiform [MedDRA:10008748]
Other choreas [MedDRA:10008748]
Hemichorea [MedDRA:10008748]
Chorea (in some patients) [OMIM:Chorea (in some patients)]
Choreic movements (10 to 22% of patients) [OMIM:Choreic movements (10 to 22% of patients)]
Choreiform movements [MedDRA:10008752]
Quality:
Cross references:
Orphanet:43250 "Chorea/athetosis/choreoathetosis/choreic syndrome" [Orphanet:43250]
OMIM: "Chorea" [OMIM:Chorea]
OMIM: "Choreic movements" [OMIM:Choreic movements]
OMIM: "Choreiform movements" [OMIM:Choreiform movements]
OMIM: "Chorea (in some patients)" [OMIM:Chorea (in some patients)]
OMIM: "Choreic movements (10 to 22% of patients)" [OMIM:Choreic movements (10 to 22% of patients)]
UMLS:C0008489 "Chorea" [Orphanet:43250]
Is a (Direct Parents):
Orphanet Abnormality of movement
Orphanet Choreoathetosis
MedDRA Abnormality of movement
HPO         Involuntary movements
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)
                Involuntary movements(HPO:0004305)
                   Chorea(HPO:0002072)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Involuntary movements(HPO:0004305)
                Chorea(HPO:0002072)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Chorea(HPO:0002072)
Database Frequency: 53 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 3 (Orphanet:67047)
ACETYL-CoA ACETYLTRANSFERASE-2 DEFICIENCY (OMIM:614055)
Aceruloplasminemia (Orphanet:48818)
Alpers syndrome (Orphanet:726)
Ataxia-telangiectasia-like disorder (Orphanet:251347)
Autosomal recessive limb-girdle muscular dystrophy type 2B (Orphanet:268)
Autosomal recessive limb-girdle muscular dystrophy type 2S (Orphanet:369840)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 (OMIM:213600)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 (OMIM:615483)
Benign familial chorea (Orphanet:1429)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY (OMIM:607674)
CHOREA, BENIGN FAMILIAL (OMIM:215450)
CHOREA, BENIGN HEREDITARY (OMIM:118700)
CHOREA, REMITTING, WITH NYSTAGMUS AND CATARACT (OMIM:601372)
Congenital cataracts - facial dysmorphism - neuropathy (Orphanet:48431)
DYSTONIA WITH RINGBINDEN (OMIM:224550)
Dentatorubral pallidoluysian atrophy (Orphanet:101)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17 (OMIM:615473)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29 (OMIM:616339)
EPISODIC KINESIGENIC DYSKINESIA 2 (OMIM:611031)
Familial dyskinesia and facial myokymia (Orphanet:324588)
Huntington disease (Orphanet:399)
Huntington disease-like 1 (Orphanet:157941)
Huntington disease-like 2 (Orphanet:98934)
Huntington disease-like 3 (Orphanet:157946)
Infantile dystonia-parkinsonism (Orphanet:238455)
Juvenile Huntington disease (Orphanet:248111)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
Leigh syndrome (Orphanet:506)
METACHROMATIC LEUKODYSTROPHY (OMIM:250100)
MYOPATHY WITH EXTRAPYRAMIDAL SIGNS (OMIM:615673)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Menkes disease (Orphanet:565)
Methylmalonic acidemia with homocystinuria, type cblX (Orphanet:369962)
Monosomy 18q (Orphanet:1600)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B (OMIM:610217)
Niemann-Pick disease type C (Orphanet:646)
OLIVOPONTOCEREBELLAR ATROPHY V (OMIM:164700)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2B (OMIM:612389)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2C (OMIM:612390)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Pontocerebellar hypoplasia type 8 (Orphanet:324569)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
RETT SYNDROME, CONGENITAL VARIANT (OMIM:613454)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 (OMIM:606002)
Sneddon syndrome (Orphanet:820)
Spinocerebellar ataxia type 1 (Orphanet:98755)
Spinocerebellar ataxia type 17 (Orphanet:98759)
Spinocerebellar ataxia type 7 (Orphanet:94147)
Spinocerebellar ataxia with axonal neuropathy type 2 (Orphanet:64753)
X-linked dystonia-parkinsonism (Orphanet:53351)
[DEL] LEIGH SYNDROME, X-LINKED (OMIM:308930)