{"orpha":98684,"name":"Craniostenosis with strabismus","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-98684/","orphanet_url":"https://www.orpha.net/en/disease/detail/98684","names":{"fr":{"name":"Craniosynostose avec strabisme"},"de":{"name":"Kraniostenose mit assoziiertem Strabismus"},"es":{"name":"Craneostenosis asociada con estrabismo"},"it":{"name":"Craniostenosi associata a strabismo"},"nl":{"name":"Craniostenose met strabisme"},"pt":{"name":"Cranioestenose associada com estrabismo"},"pl":{"name":"Kraniostenoza związana z zezem"},"cs":{"name":"Kraniostenózy se strabismem"},"uk":{"name":"Краніостеноз з косоокістю"},"zh":{"name":"斜视狭颅症"},"tr":{"name":"Şaşılık ile seyreden kraniostenoz"}},"xrefs":[{"source":"UMLS","code":"C5681696","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":98683,"name":"Syndromic disorder with strabismus","classifications":[189]},{"orpha":522520,"name":"Syndromic genetic disorder with strabismus","classifications":[156]}],"children":[{"orpha":87,"name":"Apert syndrome","type":"Malformation syndrome"},{"orpha":207,"name":"Crouzon syndrome","type":"Malformation syndrome"},{"orpha":93262,"name":"Crouzon syndrome-acanthosis nigricans syndrome","type":"Malformation syndrome"},{"orpha":35099,"name":"Non-syndromic bicoronal craniosynostosis","type":"Morphological anomaly"},{"orpha":3366,"name":"Non-syndromic metopic craniosynostosis","type":"Morphological anomaly"},{"orpha":35093,"name":"Non-syndromic sagittal craniosynostosis","type":"Morphological anomaly"},{"orpha":710,"name":"Pfeiffer syndrome","type":"Malformation syndrome"},{"orpha":794,"name":"Saethre-Chotzen syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}