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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Osteochondrodysplasias > Hyperostosis, Cortical, Congenital
Musculoskeletal Diseases > Bone Diseases > Bone Diseases, Developmental > Osteochondrodysplasias > Hyperostosis, Cortical, Congenital
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Hyperostosis, Cortical, Congenital
Musculoskeletal Diseases > Bone Diseases > Hyperostosis > Hyperostosis, Cortical, Congenital

Preferred term

Hyperostosis, Cortical, Congenital  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Caffey De Toni Silvermann Syndrome
  • Caffey-De Toni-Silvermann Syndrome
  • Caffey Disease
  • Caffey's Disease, Familial
  • Congenital Cortical Hyperostoses
  • Congenital Cortical Hyperostosis
  • Congenital Hyperostoses, Cortical
  • Congenital Hyperostosis, Cortical
  • Cortical Congenital Hyperostoses
  • Cortical Congenital Hyperostosis
  • Cortical Hyperostoses, Congenital
  • Cortical Hyperostoses, Infantile
  • Cortical Hyperostosis, Congenital
  • Cortical Hyperostosis, Infantile
  • Disease, Caffey
  • Disease, Familial Caffey's
  • Familial Caffey Disease
  • Familial Caffey's Disease
  • Familial Caffeys Disease
  • Familial Infantile Cortical Hyperostosis
  • Hyperostoses, Congenital Cortical
  • Hyperostoses, Cortical Congenital
  • Hyperostoses, Infantile Cortical
  • Hyperostosis, Congenital Cortical
  • Hyperostosis, Cortical Congenital
  • Hyperostosis, Infantile Cortical
  • Infantile Cortical Hyperostoses
  • Infantile Cortical Hyperostosis
  • Syndrome, Caffey-De Toni-Silvermann

Note

  • cortical refers to cortex of bone; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES

Scope note

  • 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)

History note

  • 91; was HYPEROSTOSIS, CORTICAL CONGENITAL 1964-90

In other languages

URI

http://www.yso.fi/onto/mesh/D006958

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