OBO ID: DOID:4257
Term Name: Caffey disease Search Ontology:
Synonyms:
  • cortical congenital hyperostosis
  • infantile cortical hyperostosis
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. http://en.wikipedia.org/wiki/Infantile_cortical_hyperostosis
References:
Ontology: Human Disease   (DOID:4257)
OTHER Caffey disease PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
COL1A1 Caffey disease 114000
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None