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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:C118423, 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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory