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The disease is associated with mutations in the FGFR2 gene.\" [url:http\\://en.wikipedia.org/wiki/Crouzon_syndrome, url:http\\://ghr.nlm.nih.gov/condition/crouzon-syndrome, url:https\\://www.faces-cranio.org/crouzon]","descendants":[],"doid":"DOID:2339","name":"Crouzon syndrome","parents":["DOID:2340"],"synonyms":{"exact":["Craniofacial Dysostosis"],"related":["Crouzon's disease"]},"xrefs":{"gard":"6206","icd10":"Q75.1","mesh":"D003394","mim":"123500","ncit":"C84653","snomedct_us_2025_09_01":"28861008","umls_cui":"C0010273"}},"hpo":[{"disease_name":"Crouzon syndrome","inheritance":{"biocuration":[{"date":"2009-02-17","name":"HPO:iea"},{"date":"2023-01-31","name":"HPO:probinson"}],"evidence":"PCS","hpo_id":"HP:0000006","hpo_name":"Autosomal dominant 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