| Metadata | |
|---|---|
| ID | DOID:4257 |
| Name | Caffey disease |
| 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. http://en.wikipedia.org/wiki/Infantile_cortical_hyperostosis |
| Xrefs |
SNOMEDCT_US_2023_03_01:24752008 |
| Subsets |
DO_rare_slim NCIthesaurus |
| Synonyms |
cortical congenital hyperostosis [EXACT] infantile cortical hyperostosis [EXACT] |
| Parent Relationships |