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| General Information | |||
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| Term | Caffey disease | ID (Ontology) | DOID:4257 (Human 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. | ||
| Also Known As | "cortical congenital hyperostosis" ; "infantile cortical hyperostosis" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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bone disease |__bone inflammation disease |__Caffey disease |
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| Is a | bone inflammation disease | ||
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GARD:1051 ICD10CM:M89.8 MESH:D006958 MIM:114000 NCI:C84645 SNOMEDCT_US_2023_03_01:24752008 UMLS_CUI:C0020497 |
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