Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Skin Abnormalities
Ehlers-Danlos Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Ehlers-Danlos Syndrome
Preferred term
Ehlers-Danlos Syndrome, Type IV
Type
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Topical Descriptor
Broader concept
Entry terms
- EDS IV
- Ehlers Danlos Syndrome, Arterial Type
- Ehlers-Danlos Syndrome, Arterial Type
- Ehlers Danlos Syndrome, Ecchymotic Type
- Ehlers-Danlos Syndrome, Ecchymotic Type
- Ehlers Danlos Syndrome, Sack Barabas Type
- Ehlers Danlos Syndrome, Sack-Barabas Type
- Ehlers-Danlos Syndrome, Sack-Barabas Type
- Ehlers-Danlos Syndromes, Vascular
- Ehlers Danlos Syndrome Type 4, Autosomal Dominant
- Ehlers-Danlos Syndrome, Type IV, Autosomal Dominant
- Ehlers-Danlos Syndrome, Vascular
- Ehlers-Danlos Syndrome, Vascular Type
- Syndromes, Vascular Ehlers-Danlos
- Syndrome, Vascular Ehlers-Danlos
- Type IV Ehlers Danlos Syndrome
- Type IV Ehlers-Danlos Syndrome
- Vascular Ehlers Danlos Syndrome
- Vascular Ehlers-Danlos Syndrome
- Vascular Ehlers-Danlos Syndromes
- Vascular Type Ehlers-Danlos Syndrome
Scope note
- A subtype of Ehlers-Danlos syndrome (EDS) characterized by vascular pathologies, e.g., AORTIC DISSECTION in addition to common EDS findings, e.g., hyperextensible skin and joints, skin fragility and reduced wound healing capability. It is associated with mutations in collagen type III alpha 1 chain gene (COLLAGEN TYPE III).
History note
- 2023; see EHLERS-DANLOS SYNDROME 2008-2022
In other languages
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Finnish
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Ehlers-Danlos tyyppi IV
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Sack-Barabas-oireyhtymä
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vaskulaari Ehlers-Danlos-oireyhtymä
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Swedish
URI
http://www.yso.fi/onto/mesh/D000094623
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