Involuntary movements
Symptom Information:
Symptom ID: | HPO:0004305 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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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) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Involuntary movements(HPO:0004305) MedDRA: |
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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) |