{"orpha":93451,"name":"Cleidocranial dysplasia and isolated cranial ossification defect","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-93451/","orphanet_url":"https://www.orpha.net/en/disease/detail/93451","names":{"fr":{"name":"Dysplasie cleido-crânienne et défaut d'ossification du crâne isolé"},"de":{"name":"Kleidokraniale Dysplasie und isolierten kranialen Ossifikationsdefekt"},"es":{"name":"Displasia cleidocraneal y defecto de osificación craneal aislado"},"it":{"name":"Displasia cleidocranica e difetto isolato dell'ossificazione del cranio"},"nl":{"name":"Cleidocraniale dysplasie en geïsoleerd craniale ossificatiedefect"},"pt":{"name":"Displasia cleidocraniana e defeito de ossificação craniana isolado"},"pl":{"name":"Grupa dysplazji obojczykowo-czaszkowych"},"cs":{"name":"Kleidokraniální dysplázie a izolované defekty kraniální osifikace"},"uk":{"name":"Клідокраніальна дисплазія та ізольований дефект окостеніння черепа"},"zh":{"name":"锁骨颅骨发育不良伴孤立型颅骨骨化缺陷"},"tr":{"name":"Kleidokraniyal displazi ve izole kraniyal ossifikasyon defekti"}},"xrefs":[{"source":"UMLS","code":"C5681593","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93419,"name":"Rare bone disease"},"parents":[{"orpha":98038,"name":"Cranial malformation","classifications":[147]},{"orpha":364526,"name":"Primary bone dysplasia","classifications":[147,156,199]}],"children":[{"orpha":1452,"name":"Cleidocranial dysplasia","type":"Malformation syndrome"},{"orpha":85199,"name":"Craniosynostosis-anal anomalies-porokeratosis syndrome","type":"Malformation syndrome"},{"orpha":3034,"name":"Delayed membranous cranial ossification","type":"Malformation syndrome"},{"orpha":60015,"name":"Enlarged parietal foramina","type":"Malformation syndrome"},{"orpha":251290,"name":"Parietal foramina with clavicular hypoplasia","type":"Malformation syndrome"},{"orpha":3472,"name":"Yunis-Varon syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}