{"orpha":1318,"name":"Campomelia, Cumming type","type":"Malformation syndrome","group":"Disorder","status":"active","flags":[],"synonyms":["Cumming syndrome"],"definition":"Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies.","note":null,"url":"https://raremap.alftech.space/d/ORPHA-1318/","orphanet_url":"https://www.orpha.net/en/disease/detail/1318","names":{"fr":{"name":"Campomélie type Cumming","synonyms":["Syndrome de Cumming"],"definition":"La campomélie de type Cumming est caractérisée par l'association d'une malformation des membres et des anomalies multiviscérales."},"de":{"name":"Kampomelie Typ Cumming","synonyms":["Cumming-Syndrom"]},"es":{"name":"Campomelia tipo Cumming","synonyms":["Síndrome de Cumming"],"definition":"La campomelia tipo Cumming está caracterizada por la asociación de defectos de las extremidades y anomalías multiviscerales."},"it":{"name":"Campomelia, tipo Cumming","synonyms":["Sindrome di Cumming"]},"nl":{"name":"Campomelie, Cumming-type","synonyms":["Syndroom van Cumming"],"definition":"Een aandoening, gekenmerkt door de associatie van ledemaat defecten en multiviscerale anomalieën."},"pt":{"name":"Campomelia, tipo Cumming","synonyms":["Síndrome Cumming"]},"pl":{"name":"Kampomelia typu Cumminga","synonyms":["Cumming syndrome"]},"cs":{"name":"Kampomelie, Cummingův typ","synonyms":["Cumming syndrome"]},"uk":{"name":"Кампомелія Каммінга","synonyms":["Синдром Каммінга"],"definition":"Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies."},"zh":{"name":"肢体弯曲Cumming型"},"tr":{"name":"Campomelia, Cumming tipi"}},"xrefs":[{"source":"OMIM","code":"211890","qualifier":"E","icd_relation":null,"validated":true},{"source":"ICD-10","code":"Q87.8","qualifier":"NTBT","icd_relation":"attributed","validated":true},{"source":"ICD-11","code":"LD24.C","qualifier":"NTBT","icd_relation":"index","validated":true,"icd11_uri":"152223075"},{"source":"MONDO","code":"0008896","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"C537966","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1859371","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"1061","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93419,"name":"Rare bone disease"},"parents":[{"orpha":93439,"name":"Campomelic dysplasia and related disorders","classifications":[147,156,199]},{"orpha":611327,"name":"Genetic multiple congenital anomalies/dysmorphic syndrome-intellectual 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