Hyperostosis, Cortical, Congenital
"Hyperostosis, Cortical, Congenital" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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)
| Descriptor ID |
D006958
|
| MeSH Number(s) |
C05.116.099.708.479 C05.116.540.400 C16.614.465
|
| Concept/Terms |
Hyperostosis, Cortical, Congenital- Hyperostosis, Cortical, Congenital
- Congenital Hyperostosis, Cortical
- Congenital Hyperostoses, Cortical
- Cortical Congenital Hyperostoses
- Hyperostoses, Cortical Congenital
- Hyperostosis, Cortical Congenital
- Cortical Congenital Hyperostosis
- Familial Caffey's Disease
- Caffey's Disease, Familial
- Disease, Familial Caffey's
- Familial Caffey Disease
- Familial Caffeys Disease
- Infantile Cortical Hyperostosis
- Cortical Hyperostoses, Infantile
- Cortical Hyperostosis, Infantile
- Hyperostoses, Infantile Cortical
- Hyperostosis, Infantile Cortical
- Infantile Cortical Hyperostoses
- Caffey Disease
- Disease, Caffey
- Familial Infantile Cortical Hyperostosis
- Caffey-De Toni-Silvermann Syndrome
- Caffey De Toni Silvermann Syndrome
- Syndrome, Caffey-De Toni-Silvermann
- Cortical Hyperostosis, Congenital
- Congenital Cortical Hyperostoses
- Congenital Cortical Hyperostosis
- Cortical Hyperostoses, Congenital
- Hyperostoses, Congenital Cortical
- Hyperostosis, Congenital Cortical
|
Below are MeSH descriptors whose meaning is more general than "Hyperostosis, Cortical, Congenital".
- Diseases [C]
- Musculoskeletal Diseases [C05]
- Bone Diseases [C05.116]
- Bone Diseases, Developmental [C05.116.099]
- Osteochondrodysplasias [C05.116.099.708]
- Hyperostosis, Cortical, Congenital [C05.116.099.708.479]
- Hyperostosis [C05.116.540]
- Hyperostosis, Cortical, Congenital [C05.116.540.400]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Infant, Newborn, Diseases [C16.614]
- Hyperostosis, Cortical, Congenital [C16.614.465]
Below are MeSH descriptors whose meaning is more specific than "Hyperostosis, Cortical, Congenital".
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