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Disease Ontology Browser
Caffey disease (DOID:4257)
Alliance: disease page
Synonyms: cortical congenital hyperostosis; infantile cortical hyperostosis
Alt IDs: OMIM:114000, ICD10CM:M89.8, MESH:D006958, NCI:C84645, UMLS_CUI:C0020497
Definition: A bone inflammation disease that causes bone changes, soft tissue swelling and irritability in infants. The disease has been associated with COL1A1 gene. It has symptom soft-tissue swelling, has symptom bone lesions, and has symptom irritability.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory