DISEASES

Disease-gene associations mined from literature

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 ...

Linkouts:  OMIM