{"orpha":1432,"name":"Autosomal dominant chorioretinopathy-microcephaly 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 Microcephaly-lymphedema-chorioretinopathy syndrome","url":"https://raremap.alftech.space/d/ORPHA-1432/","orphanet_url":"https://www.orpha.net/en/disease/detail/1432","names":{"fr":{"name":"Syndrome de choriorétinopathie-microcéphalie autosomique dominante"},"de":{"name":"Chorioretinopathie-Mikrozephalie-Syndrom, autosomal-dominantes"},"es":{"name":"Síndrome de coriorretinopatía-microcefalia, autosómica dominante"},"it":{"name":"Corioretinopatia - microcefalia, autosomica dominante"},"nl":{"name":"Autosomaal dominant chorioretinopathie – microcefalie-syndroom"},"pt":{"name":"Síndrome de coriorretinopatia-microcefalia autossómica dominante"},"pl":{"name":"Autosomalna dominująca chorioretinopatia - małogłowie"},"cs":{"name":"Syndrom zahrnující autozomálně dominantní chorioretinopatii a mikrocefalii"},"uk":{"name":"Аутосомно-домінантний синдром хоріоретинопатії-мікроцефалії"},"zh":{"name":"常染色体显性遗传脉络膜视网膜病变-小头畸形综合征"},"tr":{"name":"Otozomal dominant koriyoretinopati-mikrosefali sendromu"}},"xrefs":[{"source":"UMLS","code":"C3501946","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":2526,"name":"Microcephaly-chorioretinopathy-lymphedema syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}