<nowiki>sindrome di Fahr; ファール病; syndrome de Fahr; Fahr-Kränkt; Choroba Fahra; síndrome de Fahr; Νόσος του Fahr; Идиопатическая кальцификация базальных ганглиев 1; síndrome de Fahr; Morbus Fahr; Fahrin tauti; basal ganglia calcification; متلازمة فار; Болест на Фар; Fahrov sindrom; calcificazione idiopatica dei nuclei della base (telencefalo), anche nota come Morbo di Fahr, è una rara malattia genetica autosomica dominante; Krankheit; a rare, genetic neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement; مرض من الأمراض; хвороба; maladie se traduisant par des calcifications massives des noyaux gris centraux en l'absence d'anomalie du métabolisme du calcium; malaltia de Fahr; calcificació cerebral familiar primària; calcificació idiopàtica i familiar dels ganglis basals[; Fahr-Krankheit; Fahr-Syndrom; Striatodentale Kalzifikation; Syndrome de fahr; Maladie de Fahr; Fahr disease; childhood-onset idiopathic basal ganglia calcification; idiopathic basal ganglia calcification; Basal Ganglia Calcification, Idiopathic, 3; IBGC1; BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1; Striopallidodentate Calcinosis, Bilateral; Striopallidodentate Calcinosis, Autosomal Dominant, Adult-Onset; Cerebral Calcification, Nonarteriosclerotic, Idiopathic, Adult-Onset; Fahr Disease, Familial; Ferrocalcinosis, Cerebrovascular; Fahr Disease, Familial, Formerly; Basal Ganglia Calcification, Idiopathic, 3, Formerly; Fahr's disease; Chavany-Brunhes syndrome; Fritsche's syndrome; Familial idiopathic basal ganglia calcification; Primary familial brain calcification; Idiopathic basal ganglia calcification disease; Rodzinne zwapnienie zwojów podstawy; Zespół Chavany-Brunhesa; Sindrome de Fahr; Ferrocalcinosis cerebrovascular; Calcificaciones cerebrales no arterioscleróticas; Calcificaciones cerebrales no arterioscleroticas; Ferrocalcinosis cerebro vascular; Calcinosis de los núcleos del cerebro; Calcinosis de los nucleos del cerebro; Синдром Фара</nowiki>
basal ganglia calcification
a rare, genetic neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement
