{"orpha":2174,"name":"Hunter-Carpenter-McDonald syndrome","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Infantile neuroaxonal dystrophy","url":"https://raremap.alftech.space/d/ORPHA-2174/","orphanet_url":"https://www.orpha.net/en/disease/detail/2174","names":{"fr":{"name":"Syndrome de Hunter-Carpenter-McDonald"},"de":{"name":"Hunter-Carpenter-McDonald-Syndrom"},"es":{"name":"Síndrome de Hunter-Carpenter-McDonald"},"it":{"name":"Sindrome di Hunter-Carpenter-McDonald"},"nl":{"name":"Syndroom van Hunter-Carpenter-McDonald"},"pt":{"name":"Síndrome Hunter-Carpenter-McDonald"},"pl":{"name":"Zespół Huntera, Carpenteara i McDonalda"},"cs":{"name":"Hunterův-Carpenterův-McDonaldův syndrom","synonyms":["Hunter-Carpenter-McDonaldův syndrom"]},"uk":{"name":"Синдром Хантера-Карпентера-МакДональда"},"zh":{"name":"Hunter-Carpenter-McDonald综合征"},"tr":{"name":"Hunter-Carpenter-McDonald sendromu"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":35069,"name":"PLA2G6-related neurodegeneration, infantile-onset"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}