{"orpha":221117,"name":"Gerstmann syndrome","type":"Disease","group":"Disorder","status":"active","flags":[],"synonyms":[],"definition":"Gerstmann syndrome is a very rare neurological disorder characterized by the specific association of acalculia, finger agnosia, left-right disorientation, and agraphia, which is supposed to be secondary to a focal subcortical white matter damage in the parietal lobe.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-221117/","orphanet_url":"https://www.orpha.net/en/disease/detail/221117","names":{"fr":{"name":"Syndrome de Gerstmann","definition":"Le syndrome de Gerstmann est un trouble neurologique très rare caractérisé par l'association spécifique d'une acalculie, d'une agnosie digitale, d'une désorientation droite-gauche et d'une agraphie, qui sont supposées être secondaires à une atteinte focale sous-corticale de la substance blanche au niveau du lobe pariétal."},"de":{"name":"Gerstmann-Syndrom","definition":"Das Gerstmann-Syndrom ist eine sehr seltene neurologische Störung und gekennzeichnet durch die spezifische Assoziation von Akalkulie, Finger-Agnosie, Links-Rechts-Orientierungsstörung und Agraphie. Es wird vermutet, dass die Störung Folge eines fokalen subkortikalen Schadens der weißen Substanz im Schläfenlappen ist."},"es":{"name":"Síndrome de Gerstmann","definition":"El síndrome de Gerstmann es un trastorno neurológico muy poco frecuente que se caracteriza por la asociación específica de acalculia, agnosia digital, desorientación izquierda-derecha, y agrafia. Se considera que es secundario a un daño de la sustancia blanca focal subcortical del lóbulo parietal."},"it":{"name":"Sindrome di Gerstmann","definition":"La sindrome di Gerstmann è una malattia neurologica molto rara, caratterizzata dall'associazione tra l'acalculia, l'agnosia delle dita delle mani, il disorientamento destra-sinistra e l'agrafia. Si ritiene sia secondaria a un danno focale della sostanza bianca subcorticale del lobo parietale."},"nl":{"name":"Syndroom van Gerstmann","definition":"Een zeer zeldzame neurologische aandoening, gekenmerkt door de specifieke associatie van acalculie, agnosie van vinger, links-rechts-desoriëntatie, en agrafie, vermoedelijk secundair aan een focale beschadiging van subcorticale witte stof in pariëtaalkwab."},"pt":{"name":"Síndrome de Gerstmann"},"pl":{"name":"Zespół Gerstmanna"},"cs":{"name":"Gerstmannův syndrom"},"uk":{"name":"Синдром Герстмана","definition":"Gerstmann syndrome is a very rare neurological disorder characterized by the specific association of acalculia, finger agnosia, left-right disorientation, and agraphia, which is supposed to be secondary to a focal subcortical white matter damage in the parietal lobe."},"zh":{"name":"格斯特曼综合征","definition":"Gerstmann综合征是一种非常罕见的神经系统疾病，其特征是失算症、手指失认症、左右定向障碍和失写，这可能是顶叶皮质下白质损害的继发性表现。"},"tr":{"name":"Gerstmann sendromu"}},"xrefs":[{"source":"ICD-10","code":"F81.2","qualifier":"NTBT","icd_relation":"inclusion","validated":true},{"source":"ICD-11","code":"MB4C","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"1121787098"},{"source":"MONDO","code":"0005773","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"D005862","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0017494","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"8660","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10048608","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":98006,"name":"Rare neurologic disease","classifications":[181]}],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}