{"orpha":522540,"name":"Anterior segment developmental anomaly of genetic origin","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-522540/","orphanet_url":"https://www.orpha.net/en/disease/detail/522540","names":{"fr":{"name":"Anomalie du développement du segment antérieur de l'oeil d'origine génétique"},"de":{"name":"Genetisch bedingte Entwicklungsstörung des vorderen Augensegments"},"es":{"name":"Anomalía del desarrollo del segmento anterior de origen genético"},"it":{"name":"Anomalie dello sviluppo del segmqnto anteriore dell'occhio di origine genetica"},"nl":{"name":"Ontwikkelingsanomalie van voorste oogsegment van genetische oorsprong"},"pt":{"name":"Anomalia do desenvolvimento do segmento anterior de origem genética"},"pl":{"name":"Wada rozwojowa przedniego odcinka oka uwarunkowana genetycznie"},"cs":{"name":"Geneticky podmínaná vývojová anomálie předního segmentu oka"},"uk":{"name":"Генетично обумовлена аномалія розвитку переднього сегмента"},"zh":{"name":"遗传性前节发育异常"},"tr":{"name":"Genetik kaynaklı anterior gelişim anomalisi"}},"xrefs":[{"source":"UMLS","code":"C5681421","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":183557,"name":"Genetic developmental defect of the eye","classifications":[156]},{"orpha":522538,"name":"Rare genetic disorder of the anterior segment of the eye","classifications":[156]}],"children":[{"orpha":519276,"name":"Anterior segment developmental anomaly with extraocular manifestations","type":"Category"},{"orpha":98634,"name":"Anterior segment developmental anomaly without extraocular manifestations","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}