Chorea
Symptom Information:
Symptom ID: | HPO:0002072 | ||||||||||||||||||
Synonyms: |
|
||||||||||||||||||
Quality: | |||||||||||||||||||
Cross references: |
|
||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||
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) |