{"orpha":169163,"name":"Familial scaphocephaly syndrome","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-169163/","orphanet_url":"https://www.orpha.net/en/disease/detail/169163","names":{"fr":{"name":"Sacophocépalie syndromique familiale"},"de":{"name":"Skaphokephalie-Syndrom, familiäres"},"es":{"name":"Síndrome de escafocefalia familiar"},"it":{"name":"Sindrome da scafocefalia familiare"},"nl":{"name":"Familiale scafocefaliesyndroom"},"pt":{"name":"Síndrome de escafocefalia familiar"},"pl":{"name":"Rodzinny zespół skafocefalii/łódkogłowia"},"cs":{"name":"Familiární skafocefalie"},"uk":{"name":"Сімейний синдром скафоцефалії"},"zh":{"name":"家族性舟状头综合征"},"tr":{"name":"Ailesel skafosefali sendromu"}},"xrefs":[{"source":"MONDO","code":"0015704","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"15704","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C3267076","qualifier":"E","icd_relation":null,"validated":true},{"source":"MedDRA","code":"10072229","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":139393,"name":"Syndromic craniosynostosis","classifications":[147,156,199]}],"children":[{"orpha":1538,"name":"Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome","type":"Malformation syndrome"},{"orpha":168624,"name":"Familial scaphocephaly syndrome, McGillivray type","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}