{"orpha":207021,"name":"Rare hereditary systemic disease with peripheral 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-207021/","orphanet_url":"https://www.orpha.net/en/disease/detail/207021","names":{"fr":{"name":"Maladie systémique héréditaire avec neuropathie périphérique"},"de":{"name":"Seltene hereditäre systemische Krankheit mit peripherer Neuropathie"},"es":{"name":"Enfermedad sistémica rara hereditaria con neuropatía periférica"},"it":{"name":"Malattia sistemica ereditaria rara con neuropatia periferica"},"nl":{"name":"Zeldzame erfelijke systemische ziekte met perifere neuropathie"},"pt":{"name":"Doença rara hereditária sistémica com neuropatia periférica"},"pl":{"name":"Rzadka dziedziczna choroba układowa z neuropatią obwodową"},"cs":{"name":"Vzácná hereditární systémová onemocnění s periferní neuropatií"},"uk":{"name":"Рідкісне спадкове системне захворювання з периферичною нейропатією"},"zh":{"name":"罕见遗传性系统性疾病伴周围神经病"},"tr":{"name":"Periferik nöropati ile seyreden nadir kalıtsal sistemik hastalık"}},"xrefs":[{"source":"MONDO","code":"16134","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680813","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":207015,"name":"Rare hereditary disease with peripheral neuropathy","classifications":[156,181]}],"children":[{"orpha":85448,"name":"AGel amyloidosis","type":"Disease"},{"orpha":85447,"name":"ATTRV30M amyloidosis","type":"Clinical subtype"},{"orpha":485418,"name":"EMILIN-1-related connective tissue disease","type":"Disease"},{"orpha":31150,"name":"Tangier disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}