{"orpha":98574,"name":"Syndromic epicanthus","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-98574/","orphanet_url":"https://www.orpha.net/en/disease/detail/98574","names":{"fr":{"name":"Epicanthus syndromique"},"de":{"name":"Epikanthus, syndromaler"},"es":{"name":"Epicanto sindrómico"},"it":{"name":"Epicanto sindromico"},"nl":{"name":"Syndromale epicanthus"},"pt":{"name":"Epicanto sindromático"},"pl":{"name":"Syndromiczna zmarszczka nakątna"},"cs":{"name":"Syndromy s epikanty"},"uk":{"name":"Синдромний епікантус"},"zh":{"name":"内眦赘皮综合征"},"tr":{"name":"Sendromik epikantus"}},"xrefs":[{"source":"UMLS","code":"C5681653","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":98573,"name":"OBSOLETE: Epicanthal fold","status":"inactive"}],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98567,"name":"Rare eyelid malposition disorder","classifications":[147,189]},{"orpha":522528,"name":"Rare genetic eyelid malposition disorder","classifications":[156]}],"children":[{"orpha":48431,"name":"Congenital cataracts-facial dysmorphism-neuropathy syndrome","type":"Malformation syndrome"},{"orpha":1705,"name":"Distal duplication 14q syndrome","type":"Malformation syndrome"},{"orpha":870,"name":"Down syndrome","type":"Malformation syndrome"},{"orpha":559,"name":"Marinesco-Sjögren syndrome","type":"Disease"},{"orpha":1587,"name":"Monosomy 13q14 syndrome","type":"Malformation syndrome"},{"orpha":281,"name":"Monosomy 5p syndrome","type":"Malformation syndrome"},{"orpha":818,"name":"Smith-Lemli-Opitz syndrome","type":"Malformation syndrome"},{"orpha":881,"name":"Turner syndrome","type":"Malformation syndrome"},{"orpha":904,"name":"Williams syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}