{"orpha":98633,"name":"OBSOLETE: Goniodysgenesis","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Anterior segment developmental anomaly","url":"https://raremap.alftech.space/d/ORPHA-98633/","orphanet_url":"https://www.orpha.net/en/disease/detail/98633","names":{"fr":{"name":"OBSOLETE : Gonio-dysgénésie"},"de":{"name":"OBSOLET: Goniodysgenesie"},"es":{"name":"OBSOLETO: Goniodisgenesia"},"it":{"name":"OBSOLETO: Goniodisgenesia"},"nl":{"name":"OBSOLEET: Goniodysgenesie"},"pt":{"name":"OBSOLETO: Goniodisgenesia"},"pl":{"name":"NIEAKTUALNE: Goniodysgeneza"},"cs":{"name":"NEAKTUÁLNÍ: Goniodysgeneze"},"uk":{"name":"ЗАСТАРІЛО: Гоніодисгенез"},"zh":{"name":"弃用：前房角发育不全"},"tr":{"name":"Eski adı: Gonyodisgenezi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":88632,"name":"Anterior segment developmental anomaly"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}