{"orpha":98038,"name":"Cranial malformation","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-98038/","orphanet_url":"https://www.orpha.net/en/disease/detail/98038","names":{"fr":{"name":"Malformation crânienne"},"de":{"name":"Fehlbildung, kraniale"},"es":{"name":"Malformación craneal"},"it":{"name":"Malformazione cranica"},"nl":{"name":"Schedelmalformatie"},"pt":{"name":"Malformação do crânio"},"pl":{"name":"Wady czaszki"},"cs":{"name":"Kraniální malformace"},"uk":{"name":"Вади розвитку черепа"},"zh":{"name":"颅畸形"},"tr":{"name":"Kraniyal malformasyon"}},"xrefs":[{"source":"UMLS","code":"C5681508","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":93890,"name":"Rare developmental defect during embryogenesis"},"parents":[{"orpha":93890,"name":"Rare developmental defect during embryogenesis","classifications":[147]}],"children":[{"orpha":945,"name":"Acalvaria","type":"Malformation syndrome"},{"orpha":974,"name":"Adams-Oliver syndrome","type":"Malformation syndrome"},{"orpha":1114,"name":"Aplasia cutis congenita","type":"Malformation syndrome"},{"orpha":93451,"name":"Cleidocranial dysplasia and isolated cranial ossification defect","type":"Category"},{"orpha":2050,"name":"Cole-Carpenter syndrome","type":"Malformation syndrome"},{"orpha":1513,"name":"Craniodiaphyseal dysplasia","type":"Malformation syndrome"},{"orpha":1522,"name":"Craniometaphyseal dysplasia","type":"Malformation syndrome"},{"orpha":1531,"name":"Craniosynostosis","type":"Category"},{"orpha":1826,"name":"Frontometaphyseal dysplasia","type":"Disease"},{"orpha":97340,"name":"Hunter-McAlpine syndrome","type":"Malformation syndrome"},{"orpha":1790,"name":"Hypomandibular faciocranial dysostosis","type":"Malformation syndrome"},{"orpha":77296,"name":"Morgagni-Stewart-Morel syndrome","type":"Malformation syndrome"},{"orpha":2763,"name":"Osteocraniostenosis","type":"Malformation syndrome"},{"orpha":2780,"name":"Osteopathia striata-cranial sclerosis syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}