Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
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Movement Disorders (D009069)
Parent Node:
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Neurologic Manifestations (D009461)
..Starting node
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Dyskinesias (D020820)

       Child Nodes:
........expandAtaxia (D001259) Child126
........expandAthetosis (D001264) Child3
........expandBobble-head doll syndrome (C536241)
........expandCatalepsy (D002375)
........expandChorea (D002819) Child17
........expandChoreoathetosis/Spasticity, Episodic (C563401)
........expandDyskinesia, Drug-Induced (D004409)
........expandDyskinesia, Familial, with Facial Myokymia (C564676)
........expandDystonia (D004421) Child18
........expandEpisodic Kinesigenic Dyskinesia 2 (C567026)
........expandHyperkinesis (D006948)
........expandHypokinesia (D018476) Child1
........expandInfantile convulsions and paroxysmal choreoathetosis, familial (C535522)
........expandMental Retardation, X-Linked, Syndromic 10 (C564560)
........expandMicrocephaly pontocerebellar hypoplasia dyskinesia (C537543)
........expandMIRROR MOVEMENTS 1 (OMIM:157600)
........expandMyoclonus (D009207) Child10
........expandParoxysmal Exertion-Induced Dyskinesia And Hemolytic Anemia (C567412)
........expandPsychomotor Agitation (D011595) Child1
........expandSynkinesis (D046608) Child2
........expandTics (D020323)
........expandTremor (D014202) Child6



 Sister Nodes: 
..expandCerebrospinal Fluid Leak (D065634) Child2
..expandDecerebrate State (D003655)
..expandDiabetes Mellitus, Permanent Neonatal, With Neurologic Features (C563424)
..expandDyskinesias (D020820) Child199
..expandGait Disorders, Neurologic (D020233) Child2
..expandMeningism (D008580)
..expandNeurobehavioral Manifestations (D019954) Child701
..expandNeurogenic Inflammation (D020078)
..expandNeuromuscular Manifestations (D020879) Child103
..expandOrthostatic Intolerance (D054971) Child8
..expandPain (D010146) Child55
..expandParalysis (D010243) Child83
..expandParesis (D010291) Child10
..expandPsychophysiologic Disorders (D011602)
..expandPupil Disorders (D011681) Child20
..expandReflex, Abnormal (D012021) Child5
..expandSeizures (D012640) Child40
..expandSensation Disorders (D012678) Child478
..expandSleep Disorders (D012893) Child41
..expandSusac Syndrome (D055955)
..expandUrinary Bladder, Neurogenic (D001750)
..expandVertigo (D014717) Child5
..expandVoice Disorders (D014832) Child7
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:3530
Name:Dyskinesias
Definition:Abnormal involuntary movements which primarily affect the extremities, trunk, or jaw that occur as a manifestation of an underlying disease process. Conditions which feature recurrent or persistent episodes of dyskinesia as a primary manifestation of disease may be referred to as dyskinesia syndromes (see MOVEMENT DISORDERS). Dyskinesias are also a relatively common manifestation of BASAL GANGLIA DISEASES.
Alternative IDs:
ParentIDs:MESH:D009069|MESH:D009461
TreeNumbers:C10.228.662.262 |C10.597.350 |C23.888.592.350
Synonyms:Abnormal Movement |Abnormal Movements |Asterixis |Ballismus |Dyskinesia |Hemiballism |Hemiballismus |Involuntary Movement |Involuntary Movements |Movement, Abnormal |Movement, Involuntary |Movements, Abnormal |Movements, Involuntary
Slim Mappings:Nervous system disease|Signs and symptoms
Reference: MedGen: D020820
MeSH: D020820
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants