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DO Term : Caffey disease [DOID:4257] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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,
SNOMEDCT_US_2023_03_01:24752008,
MESH:D006958,
OMIM:114000,
infantile cortical hyperostosis,
114000,
NCI:C84645,
ICD10CM:M89.8,
GARD:1051,
UMLS_CUI:C0020497

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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