{"orpha":2060,"name":"Fukuda-Miyanomae-Nakata syndrome","type":"Malformation syndrome","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 Craniosynostosis-anal anomalies-porokeratosis syndrome","url":"https://raremap.alftech.space/d/ORPHA-2060/","orphanet_url":"https://www.orpha.net/en/disease/detail/2060","names":{"fr":{"name":"Syndrome de Fukuda-Miyanomae-Nakata"},"de":{"name":"Fukuda-Miyanomae-Nakata-Syndrom"},"es":{"name":"Síndrome de Fukuda-Miyanomae-Nakata"},"it":{"name":"Sindrome di Fukuda-Miyanomae-Nakata"},"nl":{"name":"Syndroom van Fukuda-Miyanomae-Nakata"},"pt":{"name":"Síndrome Fukuda-Miyanomae-Nakata"},"pl":{"name":"Zespół Fukuda, Miyanomae i Nakata"},"cs":{"name":"Fukudaův-Miyanomaeův-Nakataův syndrom","synonyms":["Fukuda-Miyanomae-Nakataův syndrom"]},"uk":{"name":"Синдром Фукуди-Міяномае-Наката"},"zh":{"name":"Fukuda-Miyanomae-Nakata综合征"},"tr":{"name":"Fukuda-Miyanomae-Nakata sendromu"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":85199,"name":"Craniosynostosis-anal anomalies-porokeratosis syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}