{"orpha":98634,"name":"Anterior segment developmental anomaly without extraocular manifestations","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-98634/","orphanet_url":"https://www.orpha.net/en/disease/detail/98634","names":{"fr":{"name":"Anomalie du développement du segment antérieur de l'oeil sans manifestations extra-oculaires"},"de":{"name":"Anomalie des vorderen Augensegmentes ohne extraokuläre Manifestationen"},"es":{"name":"Anomalía del desarrollo del segmento anterior sin manifestaciones extraoculares"},"it":{"name":"Iridogoniodisgenesia"},"nl":{"name":"Ontwikkelingsanomalie van voorste oogsegment zonder extraoculaire manifestaties"},"pt":{"name":"Iridogoniodisgenesia"},"pl":{"name":"Irydogoniodysgeneza"},"cs":{"name":"Iridogoniodysgeneze"},"uk":{"name":"Аномалія розвитку переднього сегмента без екстраочних проявів"},"zh":{"name":"无眼外表现眼球前区发育异常"},"tr":{"name":"Ekstraoküler belirtileri olmayan anterior segment gelişimsel anomalisi"}},"xrefs":[{"source":"MONDO","code":"11119","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681672","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":88632,"name":"Anterior segment developmental anomaly","classifications":[147,189]},{"orpha":522540,"name":"Anterior segment developmental anomaly of genetic origin","classifications":[156]},{"orpha":98631,"name":"Congenital malformation of the eye with glaucoma as a major feature","classifications":[147,189]},{"orpha":525677,"name":"Genetic congenital malformation of the eye with glaucoma as a major feature","classifications":[156]}],"children":[{"orpha":519388,"name":"Autosomal recessive anterior segment dysgenesis","type":"Malformation syndrome"},{"orpha":98978,"name":"Axenfeld anomaly","type":"Morphological anomaly"},{"orpha":69736,"name":"Bilateral acute depigmentation of the iris","type":"Disease"},{"orpha":98944,"name":"Coloboma of iris","type":"Morphological anomaly"},{"orpha":91491,"name":"Congenital ectropion uveae","type":"Malformation syndrome"},{"orpha":566,"name":"Congenital microcoria","type":"Malformation syndrome"},{"orpha":488197,"name":"Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome","type":"Disease"},{"orpha":250923,"name":"Isolated aniridia","type":"Morphological anomaly"},{"orpha":519392,"name":"Isolated iridoschisis","type":"Disease"},{"orpha":708,"name":"Peters anomaly","type":"Morphological anomaly"},{"orpha":91483,"name":"Rieger anomaly","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}