{"orpha":435,"name":"OBSOLETE: Ito hypomelanosis","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: HI syndrome","OBSOLETE: Hypomelanosis of Ito","OBSOLETE: Pigmentary mosaicism, Ito type"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Hypopigmentation of the skin","url":"https://raremap.alftech.space/d/ORPHA-435/","orphanet_url":"https://www.orpha.net/en/disease/detail/435","names":{"fr":{"name":"OBSOLETE : Hypomélanose d'Ito","synonyms":["OBSOLETE : Incontinentia pigmenti achromians","OBSOLETE : Mosaïcisme pigmentaire de type Ito"]},"de":{"name":"OBSOLET: Hypomelanose Typ Ito","synonyms":["OBSOLET: HI-Syndrom","OBSOLET: Incontinentia pigmenti Typ 1","OBSOLET: Pigmentmosaik vom Typ Ito"]},"es":{"name":"OBSOLETO: Hipomelanosis de Ito","synonyms":["OBSOLETO: Mosaicismo pigmentario tipo Ito","OBSOLETO: Síndrome HI"]},"it":{"name":"OBSOLETO: Ipomelanosi di Ito","synonyms":["OBSOLETO: Mosaicismo pigmentario, tipo Ito","OBSOLETO: Sindrome HI"]},"nl":{"name":"OBSOLEET: Ito-hypomelanosis","synonyms":["OBSOLEET: HI-syndroom","OBSOLEET: Hypomelanosis van Ito","OBSOLEET: Incontinentia pigmenti type 1","OBSOLEET: Pigmentair mozaïcisme, Ito-type"]},"pt":{"name":"OBSOLETO: Hipomelanose de Ito"},"pl":{"name":"NIEAKTUALNE: Hipomelanoza Ito","synonyms":["NIEAKTUALNE: Mozaikowatosć barwnikowy, typ Ito","NIEAKTUALNE: Nietrzymanie barwnika typu 1","NIEAKTUALNE: Zespół HI"]},"cs":{"name":"NEAKTUÁLNÍ: Ito hypomelanosis","synonyms":["NEAKTUÁLNÍ: HI syndrom","NEAKTUÁLNÍ: Incontinentia pigmenti, typ 1","NEAKTUÁLNÍ: Pigmentový mosaicismus, Itův typ"]},"uk":{"name":"ЗАСТАРІЛО: Гіпомеланоз Іто","synonyms":["ЗАСТАРІЛО: HI-синдром","ЗАСТАРІЛО: Гіпомеланоз Іто","ЗАСТАРІЛО: Пігментна мозаїчність, тип Іто"]},"zh":{"name":"弃用：无色性色素失调症","synonyms":["色素镶嵌现象Ito型"]},"tr":{"name":"Eski adı: Ito hipomelanoz","synonyms":["HI sendromu","Ito'nun hipomelanozu","Pigment mozaisizmi, Ito tipi"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":79376,"name":"Hypopigmentation of the skin"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}