{"orpha":79263,"name":"OBSOLETE: Infantile neuronal ceroid lipofuscinosis","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Hagberg-Santavuori disease","OBSOLETE: INCL","OBSOLETE: Infantile NCL","OBSOLETE: Santavuori disease","OBSOLETE: Santavuori-Haltia disease"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Neuronal ceroid lipofuscinosis","url":"https://raremap.alftech.space/d/ORPHA-79263/","orphanet_url":"https://www.orpha.net/en/disease/detail/79263","names":{"fr":{"name":"OBSOLETE : Céroïde-lipofuscinose neuronale infantile","synonyms":["OBSOLETE : CLN infantile","OBSOLETE : INCL","OBSOLETE : Maladie de Hagberg-Santavuori","OBSOLETE : Maladie de Santavuori","OBSOLETE : Maladie de Santavuori-Haltia","OBSOLETE : NCL infantile"]},"de":{"name":"OBSOLET: Ceroid-Lipofuszinose, neuronale, infantile","synonyms":["OBSOLET: Hagberg-Santavuori-Krankheit","OBSOLET: INCL","OBSOLET: NCL, infantile","OBSOLET: Santavuori-Haltia-Krankheit","OBSOLET: Santavuori-Krankheit"]},"es":{"name":"OBSOLETO: Lipofuscinosis ceroide neuronal infantil","synonyms":["OBSOLETO: Ceroidolipofuscinosis neuronal infantil","OBSOLETO: Enfermedad de Hagberg-Santavuori","OBSOLETO: Enfermedad de Santavuori","OBSOLETO: Enfermedad de Santavuori-Haltia","OBSOLETO: INCL","OBSOLETO: LCN infantil","OBSOLETO: LCNI","OBSOLETO: NCL infantil"]},"it":{"name":"OBSOLETO: Ceroidolipofuscinosi neuronale infantile","synonyms":["OBSOLETO: INCL","OBSOLETO: Malattia di Hagberg-Santavuori","OBSOLETO: Malattia di Santavuori","OBSOLETO: Malattia di Santavuori-Haltia","OBSOLETO: NCL infantile"]},"nl":{"name":"OBSOLEET: Infantiele neuronale ceroïdlipofuscinose","synonyms":["OBSOLEET: INCL","OBSOLEET: Infantiele NCL","OBSOLEET: Ziekte van Hagberg-Santavuori","OBSOLEET: Ziekte van Santavuori","OBSOLEET: Ziekte van Santavuori-Haltia"]},"pt":{"name":"OBSOLETO: Lipofuscinose ceróide neuronal do latente","synonyms":["OBSOLETO: CLN1","OBSOLETO: Doença de Hagberg-Santavuori"]},"pl":{"name":"NIEAKTUALNE: Dziecięca neuronalna lipofuscynoza ceroidowa","synonyms":["NIEAKTUALNE: Choroba Hagberga i Santavuori","NIEAKTUALNE: Choroba Santavuori","NIEAKTUALNE: Choroba Santavuori i Haltia","NIEAKTUALNE: INCL","NIEAKTUALNE: NCL dziecięca"]},"cs":{"name":"NEAKTUÁLNÍ: Infantilní neuronální ceroidlipofuscinóza","synonyms":["NEAKTUÁLNÍ: Hagbergova-Santavuoriové nemoc","NEAKTUÁLNÍ: INCL","NEAKTUÁLNÍ: Infantilní NCL","NEAKTUÁLNÍ: Santavuoriové nemoc","NEAKTUÁLNÍ: Santavuoriové-Haltiova nemoc","NEAKTUÁLNÍ: Hagberg-Santavuoriové nemoc","NEAKTUÁLNÍ: Santavuori-Haltiova nemoc"]},"uk":{"name":"ЗАСТАРІЛО: Інфантильний нейрональний цероїдний ліпофусциноз","synonyms":["ЗАСТАРІЛО: Хвороба Хагберга-Сантавуорі","ЗАСТАРІЛО: INCL","ЗАСТАРІЛО: Інфантильний НЦЛ","ЗАСТАРІЛО: Хвороба Сантавуорі","ЗАСТАРІЛО: Хвороба Сантавуорі-Халтія"]},"zh":{"name":"婴儿神经元蜡样质脂褐质沉积症","synonyms":["Hagberg-Santavuori病"]},"tr":{"name":"İnfantil nöronal seroid lipofuksinoz","synonyms":["INCL","İnfantil NCL","Santavuori hastalığı","Santavuori-Haltia hastalığı","Hagberg-Santavuori hastalığı"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":216,"name":"Neuronal ceroid lipofuscinosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}