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Cardiovascular Diseases > Vascular Diseases > Hemostatic Disorders > Ehlers-Danlos Syndrome
Hemic and Lymphatic Diseases > Hematologic Diseases > Hemorrhagic Disorders > Hemostatic Disorders > Ehlers-Danlos Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Ehlers-Danlos Syndrome
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Ehlers-Danlos Syndrome
Skin and Connective Tissue Diseases > Connective Tissue Diseases > Collagen Diseases > Ehlers-Danlos Syndrome
Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Ehlers-Danlos Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Ehlers-Danlos Syndrome

Término preferido

Ehlers-Danlos Syndrome  

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Tipo

  • mesh:Descriptor

Definición

  • A heterogeneous group of autosomally inherited COLLAGEN DISEASES caused by defects in the synthesis or structure of FIBRILLAR COLLAGEN. There are numerous subtypes: classical, hypermobility, vascular, and others. Common clinical features include hyperextensible skin and joints, skin fragility and reduced wound healing capability.

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

  • Cutis Elastica
  • Ehlers Danlos Disease
  • Ehlers-Danlos Disease

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-S9V579Z3-6

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