{"orpha":98563,"name":"Microblepharon-ablephara syndrome","type":"Clinical group","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-98563/","orphanet_url":"https://www.orpha.net/en/disease/detail/98563","names":{"fr":{"name":"Microblépharon-ablépharie"},"de":{"name":"Mikroblepharon - Ablepharie"},"es":{"name":"Síndrome de microblefaron-ablefaria"},"it":{"name":"Microblefaron - ablefaria"},"nl":{"name":"Microblefaron - ablephara-syndroom"},"pt":{"name":"Microblefaron - ablefaria"},"pl":{"name":"Microblepharon - wrodzony małe powieki"},"cs":{"name":"Syndromy s hypoplázií/aplázií očních víček"},"uk":{"name":"Синдром мікроблефарон-аблефарон"},"zh":{"name":"小眼睑-无睑畸形综合征"},"tr":{"name":"Mikroblefaron-ablefara sendromu"}},"xrefs":[{"source":"UMLS","code":"C5681656","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98561,"name":"Congenital malformation of the eyelid","classifications":[147,156,189]}],"children":[{"orpha":920,"name":"Ablepharon macrostomia syndrome","type":"Malformation syndrome"},{"orpha":2671,"name":"Neu-Laxova syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}