{"orpha":157855,"name":"HARP syndrome","type":"Clinical subtype","group":"Subtype of disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Hypoprebetalipoproteinemia-acanthocytosis-retinitis pigmentosa-pallidal degeneration syndrome"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Classic pantothenate kinase-associated neurodegeneration","url":"https://raremap.alftech.space/d/ORPHA-157855/","orphanet_url":"https://www.orpha.net/en/disease/detail/157855","names":{"fr":{"name":"Syndrome HARP","synonyms":["Syndrome d'hypoprébêtalipoprotéinémie-acanthocytose-rétinite pigmentaire-dégénérescence du globus pallidus"]},"de":{"name":"HARP-Syndrom","synonyms":["Hypopräbetalipoproteinämie - Akanthozytose - Retinitis pigmentosa - Pallidumdegeneration"]},"es":{"name":"Síndrome de HARP","synonyms":["Hipoprebetalipoproteinemia-acantocitosis-retinosis pigmentaria-degeneración del pálido","Hipoprebetalipoproteinemia-acantocitosis-retinosis pigmentaria-degeneración palidal"]},"it":{"name":"Sindrome HARP","synonyms":["Ipoprebetalipoproteinemia - acantocitosi - retinite pigmentosa - degenerazione pallidale"]},"nl":{"name":"HARP-syndroom","synonyms":["Hypo-pre-bèta-lipoproteïnemie - acanthocytose - retinitis pigmentosa - pallidale aantasting"]},"pt":{"name":"Síndrome de HARP"},"pl":{"name":"Zespół HARP","synonyms":["Hipoprebetalipoproteinemia - akantocytoza - zwyrodnienie barwnikowe siatkówki - zwyrodnienie gałki bladej"]},"cs":{"name":"HARP syndrom","synonyms":["Syndrom zahrnující hypoprebetalipoproteinémii, akantocytózu, retinitis pigmentosa a palidální degeneraci"]},"uk":{"name":"HARP-синдром","synonyms":["Синдром гіпопребеталіпопротеїнемії - акантоцитозу - пігментного ретиніту - блідої дегенерації"]},"zh":{"name":"HARP综合征","synonyms":["低脂蛋白血症-棘红细胞增多症-色素性视网膜炎-苍白球变性综合征"]},"tr":{"name":"HARP sendromu","synonyms":["Hipoprebetalipoproteinemi-akantositoz-retinitis pigmentosa-pallidal dejenerasyon sendromu"]}},"xrefs":[{"source":"UMLS","code":"C1846582","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":216866,"name":"Classic pantothenate kinase-associated neurodegeneration"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}