{"orpha":3050,"name":"OBSOLETE: Intellectual disability-hypotonia-skin hyperpigmentation syndrome","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Medrano-Roldan syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Rare syndromic intellectual disability","url":"https://raremap.alftech.space/d/ORPHA-3050/","orphanet_url":"https://www.orpha.net/en/disease/detail/3050","names":{"fr":{"name":"OBSOLETE : Syndrome de déficience intellectuelle-hypotonie-hyperpigmentation","synonyms":["OBSOLETE : Syndrome de Medrano-Roldan"]},"de":{"name":"OBSOLET: Intelligenzminderung-Hypotonie-Hyperpigmentierung-Syndrom","synonyms":["OBSOLET: Medrano-Roldan-Syndrom"]},"es":{"name":"OBSOLETO: Síndrome de discapacidad intelectual-hipotonía-hiperpigmentación de la piel","synonyms":["OBSOLETO: Síndrome de Medrano-Roldan"]},"it":{"name":"OBSOLETO: Sindrome disabilità intellettiva-ipotonia-iperpigmentazione","synonyms":["OBSOLETO: Sindrome di Medrano-Roldan"]},"nl":{"name":"OBSOLEET: Intellectuele achterstand - hypotonie - hyperpigmentatie van huid-syndroom","synonyms":["OBSOLEET: Syndroom van Medrano-Roldan"]},"pt":{"name":"OBSOLETO: Síndrome de perturbação do desenvolvimento intelectual-hipotonia-hiperpigmentação cutânea","synonyms":["OBSOLETO: Síndrome Medrano-Roldan"]},"pl":{"name":"NIEAKTUALNE: Niepelnosprawnosc intelektualna - hipotonia - hiperpigmentacja skóry","synonyms":["NIEAKTUALNE: Zespół Medrano i Roldana"]},"cs":{"name":"NEAKTUÁLNÍ: Syndrom zahrnující mentální retardaci, hypotonii a hyperpigmentaci kůže","synonyms":["NEAKTUÁLNÍ: Medranův-Roldanův syndrom","NEAKTUÁLNÍ: Medrano-Roldanův syndrom"]},"uk":{"name":"ЗАСТАРІЛО: Синдром розумової відсталості-гіпотонії-гіперпігментації шкіри","synonyms":["ЗАСТАРІЛО: Синдром Медрано-Ролдана"]},"zh":{"name":"弃用：智力障碍-肌张力低下-皮肤色素沉着过度综合征","synonyms":["Medrano-Roldan综合征"]},"tr":{"name":"Eski adı: Zihinsel yetersizlik-hipotoni-cilt hiperpigmentasyon sendromu","synonyms":["Medrano-Roldan sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":102369,"name":"Rare syndromic intellectual disability"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}