{"orpha":1420,"name":"OBSOLETE: Lethal chondrodysplasia, Moerman type","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Moerman-Vandenberghe-Fryns syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Lethal chondrodysplasia","url":"https://raremap.alftech.space/d/ORPHA-1420/","orphanet_url":"https://www.orpha.net/en/disease/detail/1420","names":{"fr":{"name":"OBSOLETE : Chondrodysplasie létale type Moerman","synonyms":["OBSOLETE : Syndrome de Moerman-Vandenberghe-Fryns"]},"de":{"name":"OBSOLET: Chondrodysplasie, letale, Typ Moerman","synonyms":["OBSOLET: Moerman-Vandenberghe-Fryns-Syndrom"]},"es":{"name":"OBSOLETO: Condrodisplasia letal tipo Moerman","synonyms":["OBSOLETO: Síndrome de Moerman-Vandenberghe-Fryns"]},"it":{"name":"OBSOLETO: Condrodisplasia letale, tipo Moerman","synonyms":["OBSOLETO: Sindrome di Moerman-Van den Berghe-Fryns"]},"nl":{"name":"OBSOLEET: Letale chondrodysplasie, Moerman-type","synonyms":["OBSOLEET: Moerman-Vandenberghe-Frynssyndroom"]},"pt":{"name":"OBSOLETO: Condrodisplasia letal, tipo Moerman","synonyms":["OBSOLETO: Síndrome Moerman-Vandenberghe-Fryns"]},"pl":{"name":"NIEAKTUALNE: Smiertelna chondrodysplazja typu Moermana","synonyms":["NIEAKTUALNE: Zespół Moermana, Vandenberghe i Frynsa"]},"cs":{"name":"NEAKTUÁLNÍ: Letální chondrodysplázie, Moermanův typ","synonyms":["NEAKTUÁLNÍ: Moermanův-Vandenbergheův-Frynsův syndrom","NEAKTUÁLNÍ: Moerman-Vandenbergh-Frynsův syndrom"]},"uk":{"name":"ЗАСТАРІЛО: Летальна хондродисплазія, тип Моермана","synonyms":["ЗАСТАРІЛО: Синдром Мурмана-Ванденберге-Фринса"]},"zh":{"name":"弃用：致命性软骨发育不良Moerman型","synonyms":["Moerman-Vandenberghe-Fryns综合征"]},"tr":{"name":"Eski adı: Letal kondrodisplazi, Moerman tipi","synonyms":["Moerman-Vandenberghe-Fryns sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":93465,"name":"Lethal chondrodysplasia"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}