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Echinobase
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,

Echinobase Genes :


OMIM:
MIM:114000 - caffey disease

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

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