{"orpha":98562,"name":"Cryptophthalmia","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-98562/","orphanet_url":"https://www.orpha.net/en/disease/detail/98562","names":{"fr":{"name":"Cryptophtalmie"},"de":{"name":"Kryptophthalmie"},"es":{"name":"Criptoftalmia"},"it":{"name":"Criptoftalmia"},"nl":{"name":"Cryptoftalmie"},"pt":{"name":"Criptoftalmia"},"pl":{"name":"Skrytoocze"},"cs":{"name":"Kryptoftalmie"},"uk":{"name":"Криптофтальмія"},"zh":{"name":"隐眼"},"tr":{"name":"Kriptoftalmi"}},"xrefs":[{"source":"ICD-11","code":"LA14.01","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"740223582"},{"source":"MONDO","code":"0020153","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C0311249","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"10505","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10011497","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":98561,"name":"Congenital malformation of the eyelid","classifications":[147,156,189]}],"children":[{"orpha":2052,"name":"Fraser syndrome","type":"Malformation syndrome"},{"orpha":91396,"name":"Isolated cryptophthalmia","type":"Morphological anomaly"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}