{"orpha":71519,"name":"Psychogenic movement disorders","type":"Clinical syndrome","group":"Disorder","status":"active","flags":[],"synonyms":["Psychogenic dystonia"],"definition":"A rare neurologic disease characterized by the manifestation of an underlying psychiatric illness or malingering, and that cannot be attributed to any known structural or neurochemical diseases. Most cases fall in the psychiatric diagnostic category of conversion disorder, also referred to as functional neurological symptom disorder.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-71519/","orphanet_url":"https://www.orpha.net/en/disease/detail/71519","names":{"fr":{"name":"Mouvements anormaux psychogènes","synonyms":["Dystonie psychogène"],"definition":"Maladie neurologique rare caractérisée par la manifestation d'une maladie psychiatrique sous-jacente ou d'une simulation qui ne peut être attribuée à aucune maladie structurelle ou neurochimique connue. La plupart des cas relèvent de la catégorie diagnostique psychiatrique du trouble de symptôme neurologique fonctionnel, précédemment connu sous le nom de trouble de conversion."},"de":{"name":"Psychogene Bewegungsstörungen","synonyms":["Dystonie, psychogene"],"definition":"Eine seltene neurologische Erkrankung, die durch die Manifestation einer psychiatrischen Grunderkrankung oder durch Simulationen gekennzeichnet ist und nicht auf bekannte strukturelle oder neurochemische Erkrankungen zurückgeführt werden kann. Die meisten Fälle fallen unter die psychiatrische Diagnosekategorie der Konversionsstörung, die auch als funktionelle neurologische Symptomstörung bezeichnet wird."},"es":{"name":"Trastornos del movimiento psicógenos","definition":"Es una enfermedad neurológica poco frecuente caracterizada por la manifestación de un trastorno psiquiátrico subyacente o simulación, y que no puede ser atribuida a ninguna enfermedad estructural o neuroquímica conocida. La mayoría de los casos pertenecen a la categoría de diagnóstico psiquiátrico de trastorno de conversión, también conocido como trastorno funcional de síntomas neurológicos."},"it":{"name":"Disturbi psicogeni del movimento","synonyms":["Distonia psicogena"],"definition":"I disturbi psicogeni del movimento (PMD) consistono in una malattia neurologica rara, e sono i sintomi di una malattia psichiatrica o di una sua simulazione, non essendo attribuibili a malattie strutturali o neurochimiche note. La maggior parte dei pazienti rientra nella categoria diagnostica psichiatrica del disturbo di conversione, anche definito disturbo da sintomi neurologici funzionali."},"nl":{"name":"Psychogene bewegingsstoornissen","synonyms":["Psychogene dystonie"],"definition":"Een zeldzame neurologische ziekte die gekarakteriseerd wordt door de manifestatie van een onderliggende psychiatrische ziekte of simulatie, en die niet kan toegeschreven worden aan een gekende structurele of neurochemische ziekte. De meeste gevallen vallen onder de psychiatrische diagnostische categorie van conversiestoornis, ook gekend als functioneel-neurologisch-symptoomstoornis."},"pt":{"name":"Alterações do movimento psicogénicas","synonyms":["Distonia psicogénica"]},"pl":{"name":"Psychogenne zaburzenia ruchu","synonyms":["Dystonia psychogenna"]},"cs":{"name":"Psychogenní poruchy hybnosti","synonyms":["Psychogenní dystonie"]},"uk":{"name":"Психогенні рухові розлади","synonyms":["Психогенна дистонія"],"definition":"A rare neurologic disease characterized by the manifestation of an underlying psychiatric illness or malingering, and that cannot be attributed to any known structural or neurochemical diseases. Most cases fall in the psychiatric diagnostic category of conversion disorder, also referred to as functional neurological symptom disorder."},"zh":{"name":"心因性运动障碍","synonyms":["心因性肌张力障碍"]},"tr":{"name":"Psikojenik hareket bozuklukları","synonyms":["Psikojenik distoni"]}},"xrefs":[{"source":"ICD-10","code":"F44.4","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"8A0Y","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"1905355308"},{"source":"MONDO","code":"0019114","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0752208","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10072376","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":102003,"name":"Rare movement disorder","classifications":[181]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":["Adolescent","Adult","Childhood","Elderly"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"Unknown","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET_[EXPERT]"}],"phenotypes":{"validation_status":"y","online":"y","validation_date":"2016-06-01","source":null,"terms":[{"hpo":"HP:0100022","label":"Abnormality of movement","frequency":"Very frequent (99-80%)","criteria":null},{"hpo":"HP:0002167","label":"Abnormality of speech or vocalization","frequency":"Frequent (79-30%)","criteria":null},{"hpo":"HP:0001288","label":"Gait disturbance","frequency":"Frequent (79-30%)","criteria":null}]}}