Human genes for Caffey disease
Caffey disease [DOID:4257]
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.
Synonyms: Caffey disease, Caffey disorder, Caffey syndrome, DOID:4257, cortical congenital hyperostosis ...