{"orpha":65798,"name":"Goodman syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["ACPS4","Acrocephalopolysyndactyly type 4"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Carpenter syndrome","url":"https://raremap.alftech.space/d/ORPHA-65798/","orphanet_url":"https://www.orpha.net/en/disease/detail/65798","names":{"fr":{"name":"Syndrome de Goodman","synonyms":["ACPS4","Acro-céphalo-syndactylie type 4"]},"de":{"name":"Goodman-Syndrom","synonyms":["ACPS4","Akrozephalopolysyndaktylie Typ 4"]},"es":{"name":"Síndrome de Goodman","synonyms":["ACPS 4","Acrocefalopolisindactilia tipo 4"]},"it":{"name":"Sindrome di Goodman","synonyms":["ACPS4","Acrocefalopolisindattilia, tipo 4"]},"nl":{"name":"Syndroom van Goodman","synonyms":["ACPS 4","Acrocefalopolysyndactylie type 4"]},"pt":{"name":"Síndrome Goodman","synonyms":["ACPS4","Acrocefalopolissindactilia tipo 4"]},"pl":{"name":"Zespół Goodmana","synonyms":["ACPS4","Akrocefalopolisyndaktylia typu 4"]},"cs":{"name":"Goodmanův syndrom","synonyms":["ACPS4","Akrocefalopolysyndaktylie, typ 4"]},"uk":{"name":"Синдром Гудмена","synonyms":["ACPS4","Акроцефалополісиндактилія 4 типу"]},"zh":{"name":"Goodman综合征","synonyms":["尖头多指（趾）并指（趾）畸形4型"]},"tr":{"name":"Goodman sendromu","synonyms":["ACPS4","Akrosefalopolisindaktili tip 4"]}},"xrefs":[{"source":"OMIM","code":"201020","qualifier":"E","icd_relation":null,"validated":true},{"source":"ICD-10","code":"Q87.0","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"MONDO","code":"0008711","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0265303","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"2549","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":65759,"name":"Carpenter syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}