Concept information
Preferred term
Hyperostosis, Cortical, Congenital
Type
-
mesh:Descriptor
Definition
- A disease of young infants characterized by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (Dorland, 27th ed)
Broader concept
Entry terms
- Caffey-De Toni-Silvermann Syndrome
- Caffey Disease
- Congenital Hyperostosis, Cortical
- Cortical Congenital Hyperostosis
- Cortical Hyperostosis, Congenital
- Familial Caffey's Disease
- Familial Infantile Cortical Hyperostosis
- Infantile Cortical Hyperostosis
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Hyperostose corticale infantile de Caffey-Silverman
-
Maladie de Caffey
-
Syndrome de Caffey-De Toni-Silvermann
URI
http://data.loterre.fr/ark:/67375/JVR-MZ7543JC-V
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