{"orpha":3362,"name":"OBSOLETE: Trichomegaly-cataract-hereditary spherocytosis syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Goldstein-Hutt syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Familial isolated trichomegaly","url":"https://raremap.alftech.space/d/ORPHA-3362/","orphanet_url":"https://www.orpha.net/en/disease/detail/3362","names":{"fr":{"name":"OBSOLETE : Syndrome de trichomégalie-cataracte-sphérocytose","synonyms":["OBSOLETE : Syndrome de Goldstein-Hutt"]},"de":{"name":"OBSOLET: Trichomegalie-Katarakt-hereditäre Sphärozytose-Syndrom","synonyms":["OBSOLET: Goldstein-Hutt-Syndrom"]},"es":{"name":"OBSOLETO: Síndrome de tricomegalia-catarata-esferocitosis hereditaria","synonyms":["OBSOLETO: Síndrome de Goldstein-Hutt"]},"it":{"name":"OBSOLETO: Sindrome tricomegalia-cataratta-sferocistosi ereditaria","synonyms":["OBSOLETO: Sindrome di Goldstein-Hutt"]},"nl":{"name":"OBSOLEET: Trichomegalie - cataract - erfelijke sferocytose-syndroom","synonyms":["OBSOLEET: Syndroom van Goldstein-Hutt"]},"pt":{"name":"OBSOLETO: Síndrome de tricomegalia-catarata-esferocitose hereditária","synonyms":["OBSOLETO: Síndrome Goldstein-Hutt"]},"pl":{"name":"NIEAKTUALNE: Trichomegalia - zacma - sferocytoza dziedziczna","synonyms":["NIEAKTUALNE: Zespół Goldsteina i Hutta"]},"cs":{"name":"NEAKTUÁLNÍ: Syndrom zahrnující trichomegalii, kataraktu a dědičnou sférocytózu","synonyms":["OBSOLETE: Goldstein-Hutt syndrome"]},"uk":{"name":"ЗАСТАРІЛО: Синдром трихомегалії-катаракти-спадкового сфероцитозу","synonyms":["ЗАСТАРІЛО: Синдром Гольдштейна-Хатта"]},"zh":{"name":"弃用：睫毛粗长症-白内障-遗传性球形红细胞增多综合征","synonyms":["Goldstein-Hutt综合征"]},"tr":{"name":"Eski adı: Trikomegali-katarakt-kalıtsal sferositoz sendromu","synonyms":["Goldstein-Hutt sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":411788,"name":"Familial isolated trichomegaly"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}