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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Osteochondrodysplasias > Ellis-Van Creveld Syndrome
Musculoskeletal Diseases > Bone Diseases > Bone Diseases, Developmental > Osteochondrodysplasias > Ellis-Van Creveld Syndrome
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Ectodermal Dysplasia > Ellis-Van Creveld Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Ectodermal Dysplasia > Ellis-Van Creveld Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Ectodermal Dysplasia > Ellis-Van Creveld Syndrome
Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ectodermal Dysplasia > Ellis-Van Creveld Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ectodermal Dysplasia > Ellis-Van Creveld Syndrome

Preferred term

Ellis-Van Creveld Syndrome  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Chondroectodermal Dysplasia
  • Chondroectodermal Dysplasias
  • Dysplasia, Chondroectodermal
  • Dysplasia, Ellis-Van Creveld
  • Dysplasia, Mesoectodermal
  • Ellis Van Creveld Dysplasia
  • Ellis-Van Creveld Dysplasia
  • Mesoectodermal Dysplasia
  • Mesoectodermal Dysplasias

Note

  • do not use /congen & do not coord with INFANT, NEWBORN, DISEASES

Scope note

  • Dwarfism occurring in association with defective development of skin, hair, and teeth, polydactyly, and defect of the cardiac septum. (Dorland, 27th ed)

History note

  • 65(63)

In other languages

URI

http://www.yso.fi/onto/mesh/D004613

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