About: Caffey disease

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

OMIM mapping confirmed by DO. [SN].

Attributes	Values
type	Class
subClassOf	bone inflammation disease nodeID://b50952811
label	Caffey disease
comment	OMIM mapping confirmed by DO. [SN].
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:4257
database_cross_reference	GARD:1051 ICD10CM:M89.8 MESH:D006958 NCI:C84645 OMIM:114000 SNOMEDCT_US_2021_09_01:24752008 UMLS_CUI:C0020497
has_exact_synonym	cortical congenital hyperostosis (en) infantile cortical hyperostosis (en)
has_obo_namespace	disease_ontology
in_subset	NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115	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.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50952812

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