{"orpha":140474,"name":"Autosomal dominant hereditary sensory and autonomic neuropathy","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-140474/","orphanet_url":"https://www.orpha.net/en/disease/detail/140474","names":{"fr":{"name":"Neuropathie sensitive et autonomique héréditaire autosomique dominante"},"de":{"name":"Neuropathie, autonome hereditäre sensorische, autosomal-dominant"},"es":{"name":"Neuropatía sensitiva autonómica hereditaria autosómica dominante"},"it":{"name":"Neuropatia sensoriale e autonomica ereditaria autosomica dominante"},"nl":{"name":"Autosomaal dominante erfelijke sensorische en autonome neuropathie"},"pt":{"name":"Neuropatia sensitiva e autonómica hereditária autossómica dominante"},"pl":{"name":"Autosomalna dominująca dziedziczna neuropatia czuciowa i autonomiczna"},"cs":{"name":"Autozomálně dominantní hereditární senzorická a autonomní neuropatie"},"uk":{"name":"Аутосомно-домінантна спадкова сенсорна та вегетативна нейропатія"},"zh":{"name":"常染色体显性遗传感觉和自主神经病变"},"tr":{"name":"Otozomal dominant kalıtsal duyusal ve otonom nöropati"}},"xrefs":[{"source":"MONDO","code":"15365","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680674","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19928","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":140471,"name":"Hereditary sensory and autonomic neuropathy","classifications":[156,181]}],"children":[{"orpha":653728,"name":"Congenital insensitivity to pain syndrome, Marsili type","type":"Disease"},{"orpha":36386,"name":"Hereditary sensory and autonomic neuropathy type 1","type":"Disease"},{"orpha":139564,"name":"Hereditary sensory and autonomic neuropathy type 1B","type":"Disease"},{"orpha":391397,"name":"Hereditary sensory and autonomic neuropathy type 7","type":"Disease"},{"orpha":456318,"name":"Hereditary sensory neuropathy-deafness-dementia syndrome","type":"Disease"},{"orpha":397606,"name":"PrP systemic amyloidosis","type":"Disease"},{"orpha":90026,"name":"Primary erythromelalgia","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Autosomal dominant"],"onset":[],"prevalence":[],"phenotypes":null}