Hyperostosis, Cortical, Congenital

History

Agammaglobulinemia

Clostridium cellulolyt

Hyperostosis, Cortical

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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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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 related to "Hyperostosis, Cortical, Congenital".

Below are MeSH descriptors whose meaning is more specific than "Hyperostosis, Cortical, Congenital".

publications

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This graph shows the total number of publications written about "Hyperostosis, Cortical, Congenital" by people in UAMS Profiles by year, and whether "Hyperostosis, Cortical, Congenital" was a major or minor topic of these publications.

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