{"orpha":140477,"name":"Autosomal recessive 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-140477/","orphanet_url":"https://www.orpha.net/en/disease/detail/140477","names":{"fr":{"name":"Neuropathie sensitive et autonomique héréditaire autosomique récessive"},"de":{"name":"Neuropathie, autonome hereditäre sensorische,autosomal-rezessiv"},"es":{"name":"Neuropatía sensitiva autonómica hereditaria autosómica recesiva"},"it":{"name":"Neuropatia sensoriale e autonomica ereditaria autosomica recessiva"},"nl":{"name":"Autosomaal recessieve erfelijke sensorische en autonome neuropathie"},"pt":{"name":"Neuropatia sensitiva e autonómica hereditária autossómica recessiva"},"pl":{"name":"Autosomalna recesywna dziedziczna neuropatia czuciowa i autonomiczna"},"cs":{"name":"Autozomálně recesivní hereditární senzorická a autonomní neuropatie"},"uk":{"name":"Аутосомно-рецесивна спадкова сенсорна та вегетативна нейропатія"},"zh":{"name":"常染色体隐性遗传感觉自主神经障碍"},"tr":{"name":"Otozomal resesif kalıtsal duyusal ve otonom nöropati"}},"xrefs":[{"source":"MONDO","code":"15366","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680675","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19929","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":401993,"name":"Cold-induced sweating syndrome-hyperthermia spectrum","type":"Clinical group"},{"orpha":653728,"name":"Congenital insensitivity to pain syndrome, Marsili type","type":"Disease"},{"orpha":453510,"name":"Congenital insensitivity to pain with severe intellectual disability","type":"Disease"},{"orpha":88642,"name":"Congenital insensitivity to pain-anosmia-neuropathic arthropathy","type":"Disease"},{"orpha":1764,"name":"Familial dysautonomia","type":"Disease"},{"orpha":320385,"name":"Hereditary sensory and autonomic neuropathy due to TECPR2 mutation","type":"Disease"},{"orpha":970,"name":"Hereditary sensory and autonomic neuropathy type 2","type":"Disease"},{"orpha":642,"name":"Hereditary sensory and autonomic neuropathy type 4","type":"Disease"},{"orpha":64752,"name":"Hereditary sensory and autonomic neuropathy type 5","type":"Disease"},{"orpha":314381,"name":"Hereditary sensory and autonomic neuropathy type 6","type":"Disease"},{"orpha":478664,"name":"Hereditary sensory and autonomic neuropathy type 8","type":"Disease"},{"orpha":139573,"name":"Hereditary sensory and autonomic neuropathy with deafness and global delay","type":"Disease"},{"orpha":139578,"name":"Mutilating hereditary sensory neuropathy with spastic paraplegia","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Autosomal recessive"],"onset":[],"prevalence":[],"phenotypes":null}