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, Caffey diseases, DOID:4257 ...
Linkouts: OMIM