{"orpha":207025,"name":"Rare hereditary neurologic 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-207025/","orphanet_url":"https://www.orpha.net/en/disease/detail/207025","names":{"fr":{"name":"Maladie neurologique héréditaire avec neuropathie périphérique"},"de":{"name":"Seltene erbliche neurologische Krankheit mit peripherer Neuropathie"},"es":{"name":"Enfermedad neurológica rara hereditaria con neuropatía periférica"},"it":{"name":"Malattia neurologica ereditaria rara con neuropatia periferica"},"nl":{"name":"Zeldzame erfelijke neurologische ziekte met perifere neuropathie"},"pt":{"name":"Doença rara hereditária neurológica com neuropatia periférica"},"pl":{"name":"Rzadka dziedziczna choroba neurologiczna z neuropatią obwodową"},"cs":{"name":"Vzácná hereditární neurologická onemocnění s periferní neuropatií"},"uk":{"name":"Рідкісне спадкове неврологічне захворювання з периферичною нейропатією"},"zh":{"name":"罕见遗传性神经性疾病伴周围神经病"},"tr":{"name":"Periferik nöropati ile seyreden nadir kalıtsal nörolojik hastalık"}},"xrefs":[{"source":"MONDO","code":"16135","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680816","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":1239,"name":"Behr syndrome","type":"Malformation syndrome"},{"orpha":610573,"name":"CLCN6-related childhood-onset progressive neurodegeneration-peripheral neuropathy syndrome","type":"Disease"},{"orpha":207028,"name":"Cerebellar ataxia with peripheral neuropathy","type":"Category"},{"orpha":694937,"name":"Intellectual disability-peripheral neuropathy-corpus callosum abnormalities syndrome due to nudix hydrolase 2 deficiency","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}