Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:4257 - Caffey disease

Disease Ontology 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.

Synonyms: cortical congenital hyperostosis, infantile cortical hyperostosis

Xenbase Genes : col1a1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007244 - Caffey disease

MIM:
MIM:114000 - CAFFEY DISEASE; CAFYD

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): bone inflammation disease (is_a)