|OBO ID: DOID:4257|
|Term Name:||Caffey disease||Search Ontology:|
|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|
|Ontology:||Human Disease (DOID:4257)|
|is a type of:||
OTHER Caffey disease PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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