{"orpha":2129,"name":"OBSOLETE: Hemihypertrophy-intestinal web-corneal opacity syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: HIPO syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Multiple congenital anomalies/dysmorphic syndrome without intellectual disability","url":"https://raremap.alftech.space/d/ORPHA-2129/","orphanet_url":"https://www.orpha.net/en/disease/detail/2129","names":{"fr":{"name":"OBSOLETE : Syndrome d'hémihypertrophie-bride intestinale-opacités cornéennes","synonyms":["OBSOLETE : Syndrome HIPO"]},"de":{"name":"OBSOLET: Hemihypertrophie-intestinales Netz-Hornhauttrübung-Syndrom","synonyms":["OBSOLET: HIPO-Syndrom"]},"es":{"name":"OBSOLETO: Síndrome de hemihipertrofia-brida intestinal-opacidad corneal","synonyms":["OBSOLETO: Síndrome de HIPO"]},"it":{"name":"OBSOLETO: emi-ipertrofia-briglia intestinale-opacità corneali","synonyms":["OBSOLETO: Sindrome HIPO"]},"nl":{"name":"OBSOLEET: Hemihypertrofie - intestinaal web - corneale opaciteit-syndroom","synonyms":["OBSOLEET: HIPO-syndroom"]},"pt":{"name":"OBSOLETO: Síndrome de hemihipertrofia-teia intestinal-opacidade da córnea","synonyms":["OBSOLETO: Síndrome HIPO"]},"pl":{"name":"NIEAKTUALNE: Przerost polowiczy - siec jelitowa - zmetnienie rogówki","synonyms":["NIEAKTUALNE: Zespół HIPO"]},"cs":{"name":"NEAKTUÁLNÍ: Syndrom hemihypertrofie, atrézie střeva a katarakty","synonyms":["OBSOLETE: HIPO syndrome"]},"uk":{"name":"ЗАСТАРІЛО: Синдром гемігіпертрофії-перетинки кишечнику-помутніння рогівки","synonyms":["ЗАСТАРІЛО: Синдром HIPO"]},"zh":{"name":"偏侧发育过度-肠道粘连-角膜斑综合征","synonyms":["HIPO综合征"]},"tr":{"name":"Eski adı: Hemihipertrofi-bağırsak ağ-korneal opasite sendromu","synonyms":["HIPO sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":102285,"name":"Multiple congenital anomalies/dysmorphic syndrome without intellectual disability"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}