{"orpha":140456,"name":"Autosomal dominant hereditary axonal motor and sensory 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-140456/","orphanet_url":"https://www.orpha.net/en/disease/detail/140456","names":{"fr":{"name":"Neuropathie sensitivo-motrice axonale héréditaire autosomique dominante"},"de":{"name":"Autosomal-dominante axonale hereditäre motorisch-sensorische Neuropathie"},"es":{"name":"Neuropatía axonal sensitivo-motora hereditaria autosómica dominante"},"it":{"name":"Neuropatia motoria e sensoriale assonale ereditaria autosomica dominante"},"nl":{"name":"Autosomaal dominante erfelijke axonale motorische en sensorische neuropathie"},"pt":{"name":"Neuropatia sensitiva e motora axonal hereditária autossómica dominante"},"pl":{"name":"Autosomalna dominująca dziedziczna aksonalna neuropatia ruchowa i czuciowa"},"cs":{"name":"Autozomálně dominantní hereditární axonální motorická a senzorická neuropatie"},"uk":{"name":"Автосомно-домінантна спадкова аксональна моторна та сенсорна нейропатія"},"zh":{"name":"常染色体显性遗传轴索运动和感觉神经病"},"tr":{"name":"Otozomal dominant kalıtsal aksonal motor ve duyusal nöropati"}},"xrefs":[{"source":"MONDO","code":"15360","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680676","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19924","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":476109,"name":"Axonal hereditary motor and sensory neuropathy","classifications":[156,181]}],"children":[{"orpha":64746,"name":"Autosomal dominant Charcot-Marie-Tooth disease type 2","type":"Clinical group"},{"orpha":1215,"name":"Autosomal dominant optic atrophy plus syndrome","type":"Disease"},{"orpha":64751,"name":"Hereditary motor and sensory neuropathy type 5","type":"Disease"},{"orpha":90120,"name":"Hereditary motor and sensory neuropathy type 6","type":"Disease"},{"orpha":90117,"name":"Hereditary motor and sensory neuropathy, Okinawa type","type":"Disease"},{"orpha":538574,"name":"Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":["Autosomal dominant"],"onset":[],"prevalence":[],"phenotypes":null}