{"orpha":99994,"name":"OBSOLETE: Complex regional pain syndrome type 2","type":"Clinical subtype","group":"Subtype of disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Complex regional pain syndrome","url":"https://raremap.alftech.space/d/ORPHA-99994/","orphanet_url":"https://www.orpha.net/en/disease/detail/99994","names":{"fr":{"name":"OBSOLETE : Causalgie"},"de":{"name":"OBSOLET: Komplexes regionales Schmerzsyndrom Typ 2","synonyms":["OBSOLET: CRPS2"]},"es":{"name":"OBSOLETO: Síndrome de dolor regional complejo tipo 2"},"it":{"name":"OBSOLETO: Sindrome del dolore regionale complesso, tipo 2"},"nl":{"name":"OBSOLEET: Complex regionaal pijnsyndroom type 2","synonyms":["OBSOLEET: CRPS2","OBSOLEET: Causalgie"]},"pt":{"name":"OBSOLETO: Causalgia"},"pl":{"name":"NIEAKTUALNE: Kompleksowy zespół bólu regionalnego typu 2","synonyms":["NIEAKTUALNE: Piekący ból"]},"cs":{"name":"NEAKTUÁLNÍ: Komplexní regionální bolestivý syndrom, typ 2","synonyms":["NEAKTUÁLNÍ: Kauzalgie"]},"uk":{"name":"Комплексний регіонарний больовий синдром, тип 2","synonyms":["Каузалгія"],"definition":"Complex regional pain syndrome type 2 (CRPS2), or causalgia is a form of complex regional pain syndrome that develops after damage to a peripheral nerve and is characterized by spontaneous pain, allodynia and hyperalgesia , not necessarily limited to the territory of the injured nerve, as well as at some point, edema, changes in skin blood flow or sudomotor dysfunction in the pain area."},"zh":{"name":"复杂区域性疼痛综合征2型","synonyms":["灼性神经痛"],"definition":"复杂性区域性疼痛综合征2型(CRPS2)或焦虑性疼痛是一种复杂的区域性疼痛综合征，发生于周围神经损伤后，以自发性疼痛、超敏和痛觉过敏为特征，不一定局限于受损神经的范围，有时还会出现痛区的水肿、皮肤血流变化或运动障碍。"},"tr":{"name":"Kompleks bölgesel ağrı sendromu tip 2","synonyms":["Kompleks bölgesel ağrı sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":83452,"name":"Complex regional pain syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}