Involuntary movements

Symptom Information:

Symptom ID: HPO:0004305
Synonyms:
Involuntary muscle contractions [HPO:0004305]
Involuntary movements [OMIM:Involuntary movements]
Quality:
Cross references:
OMIM: "Involuntary movements" [OMIM:Involuntary movements]
Is a (Direct Parents):
HPO         Abnormality of muscle physiology
HPO         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)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of movement(HPO:0100022)
                Involuntary movements(HPO:0004305)
MedDRA:
Database Frequency: 50 / 7739
Resource:

All diseases associated with this symptom:

Adult neuronal ceroid lipofuscinosis (Orphanet:79262)
Alexander disease (Orphanet:58)
Alpha-N-acetylgalactosaminidase deficiency (Orphanet:3137)
Alpha-N-acetylgalactosaminidase deficiency type 1 (Orphanet:79279)
Autosomal dominant hypocalcemia (Orphanet:428)
Benign adult familial myoclonic epilepsy (Orphanet:86814)
Benign familial infantile seizures (Orphanet:306)
CONGENITAL DISORDER OF DEGLYCOSYLATION (OMIM:615273)
Cerebrotendinous xanthomatosis (Orphanet:909)
Choreoacanthocytosis (Orphanet:2388)
De Barsy syndrome (Orphanet:2962)
Dystonia 16 (Orphanet:210571)
Encephalopathy due to prosaposin deficiency (Orphanet:139406)
Free sialic acid storage disease (Orphanet:834)
Gaucher disease (Orphanet:355)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Gorlin syndrome (Orphanet:377)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4 (OMIM:615716)
Hereditary cerebral hemorrhage with amyloidosis, Iowa type (Orphanet:324708)
Hereditary hyperekplexia (Orphanet:3197)
Holoprosencephaly (Orphanet:2162)
Hyperkalemic periodic paralysis (Orphanet:682)
Infantile convulsions and choreoathetosis (Orphanet:31709)
Infantile neuronal ceroid lipofuscinosis (Orphanet:79263)
Late infantile neuronal ceroid lipofuscinosis (Orphanet:168491)
Lathosterolosis (Orphanet:46059)
MELAS (Orphanet:550)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Monomelic amyotrophy (Orphanet:65684)
Nasu-Hakola disease (Orphanet:2770)
Neurodegeneration with brain iron accumulation (Orphanet:385)
Neuroferritinopathy (Orphanet:157846)
Nipah virus disease (Orphanet:99825)
Norrie disease (Orphanet:649)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Oculocerebrorenal syndrome (Orphanet:534)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity (Orphanet:53583)
Pelizaeus-Merzbacher disease (Orphanet:702)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Rheumatic fever (Orphanet:3099)
Riboflavin transporter deficiency (Orphanet:97229)
Severe X-linked mitochondrial encephalomyopathy (Orphanet:238329)
Sneddon syndrome (Orphanet:820)
Sudden infant death - dysgenesis of the testes (Orphanet:168593)
Vitamin B12-unresponsive methylmalonic acidemia (Orphanet:27)
Vitamin B12-unresponsive methylmalonic acidemia type mut- (Orphanet:79312)
Vitamin B12-unresponsive methylmalonic acidemia type mut0 (Orphanet:289916)
Whipple disease (Orphanet:3452)
Williams syndrome (Orphanet:904)