. _:vb50952811 . "NCI:C84645"^^ . "Caffey disease"^^ . "disease_ontology"^^ . _:vb50952811 . "SNOMEDCT_US_2021_09_01:24752008"^^ . "OMIM mapping confirmed by DO. [SN]."^^ . _:vb50952811 . "infantile cortical hyperostosis"@en . "OMIM:114000"^^ . "GARD:1051"^^ . "ICD10CM:M89.8"^^ . . "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."^^ . "cortical congenital hyperostosis"@en . "MESH:D006958"^^ . . _:vb50952811 . . "UMLS_CUI:C0020497"^^ . _:vb50952811 . "DOID:4257"^^ .