OBO ID: DOID:4257 |
Term Name: | Caffey disease | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:4257 ) |
OTHER Caffey disease PAGES
ZEBRAFISH MODELS
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PHENOTYPE
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CITATIONS: None
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