{"orpha":300337,"name":"OBSOLETE: Congenital blindness due to retinal non-attachment","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Persistent hyperplastic primary vitreous","url":"https://raremap.alftech.space/d/ORPHA-300337/","orphanet_url":"https://www.orpha.net/en/disease/detail/300337","names":{"fr":{"name":"OBSOLETE : Cécité congénitale par non-attachement de la rétine"},"de":{"name":"OBSOLET: Kongenitale Blindheit durch retinales 'non-attachment'","synonyms":["OBSOLET: Angeborene Blindheit durch Nicht-Anheftung der Netzhaut","OBSOLET: NCRNA-Krankheit","OBSOLET: Netzhautablösung, kongenitale"]},"es":{"name":"OBSOLETO: Ceguera congénita por falta de adhesión de la retina"},"it":{"name":"OBSOLETO: Cecità congenita da distacco della retina","synonyms":["OBSOLETO: Distacco retinico congenito","OBSOLETO: Distacco retinico congenito non sindromico","OBSOLETO: Malattia NCRNA"]},"nl":{"name":"OBSOLEET: Congenitale blindheid door niet-aangehechte retina","synonyms":["OBSOLEET: Congenitale niet-aangehechte retina","OBSOLEET: NCRNA-ziekte","OBSOLEET: Niet-syndromaal congenitaal niet-aangehechte retina"]},"pt":{"name":"OBSOLETO: Cegueira congénita devido à não aderência da retina"},"pl":{"name":"NIEAKTUALNE: Slepota wrodzona spowodowana odwarstwieniem siatkówki"},"cs":{"name":"NEAKTUÁLNÍ: Vrozená slepota způsobená odchlípením sítnice","synonyms":["NEAKTUÁLNÍ: Vrozené odchlípení sítnice","NEAKTUÁLNÍ: Nesyndromické vrozené odchlípení sítnice","NEAKTUÁLNÍ: NCRNA onemocnění"]},"uk":{"name":"ЗАСТАРІЛО: Вроджена сліпота через незрощення сітківки"},"zh":{"name":"弃用：因视网膜未附着而致先天失明"},"tr":{"name":"Eski adı: Retinanın yapışmamasına bağlı doğumsal körlük"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":91495,"name":"Persistent hyperplastic primary vitreous"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}