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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > 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
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > 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
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

Preferred term

Ellis-Van Creveld Syndrome  

Type

  • mesh:Descriptor

Definition

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

Broader concept

Related concepts

Synonym(s)

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

Allowable Qualifier(s)

In other languages

URI

http://data.loterre.fr/ark:/67375/JVR-QNZ9HPHJ-M

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