{"orpha":370106,"name":"Rare disorder with dystonia and other neurologic or systemic manifestation","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-370106/","orphanet_url":"https://www.orpha.net/en/disease/detail/370106","names":{"fr":{"name":"Maladie rare avec dystonie et autres manifestations neurologiques ou systémiques"},"de":{"name":"Seltene Störung mit Dystonie und weiteren neurologischen oder systemischen Manifestationen"},"es":{"name":"Enfermedad rara con distonía y otra manifestación neurológica o sistémica"},"it":{"name":"Disturbo raro con distonia e altro segno neurologico o sistemico"},"nl":{"name":"Zeldzame stoornis met dystonie en andere neurologische of systemische manifestatie"},"pt":{"name":"Doença rara com distonia e outras manifestações neurológicas ou sistémicas"},"pl":{"name":"Rzadkie zaburzenie z dystonią i innymi objawami neurologicznymi lub układowymi"},"cs":{"name":"Vzácná onemocnění s dystonií a jinými neurologickými nebo systémovými projevy"},"uk":{"name":"Рідкісний розлад з дистонією та іншими неврологічними або системними проявами"},"zh":{"name":"伴有肌张力障碍和其他神经或系统表现的罕见疾病"},"tr":{"name":"Distoni ve diğer nörolojik veya sistemik belirtiler ile seyreden nadir bozukluk"}},"xrefs":[{"source":"MONDO","code":"18265","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680969","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":68363,"name":"Rare dystonia","classifications":[181]},{"orpha":391799,"name":"Rare genetic dystonia","classifications":[156]}],"children":[{"orpha":459033,"name":"Ataxia-oculomotor apraxia type 4","type":"Disease"},{"orpha":497906,"name":"Childhood-onset basal ganglia degeneration syndrome","type":"Disease"},{"orpha":660017,"name":"Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome","type":"Disease"},{"orpha":79107,"name":"Developmental malformations-deafness-dystonia syndrome","type":"Malformation syndrome"},{"orpha":597623,"name":"IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome","type":"Disease"},{"orpha":369939,"name":"Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome","type":"Malformation syndrome"},{"orpha":905,"name":"Wilson disease","type":"Disease"},{"orpha":3464,"name":"Woodhouse-Sakati syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}