Descriptor English: | Ehlers-Danlos Syndrome, Type IV | ||||||
Descriptor Spanish: |
Síndrome de Ehlers-Danlos Tipo IV
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Descriptor Portuguese: | Síndrome de Ehlers-Danlos Tipo IV | ||||||
Descriptor French: | Without translation | ||||||
Entry term(s): |
EDS IV Ehlers Danlos Syndrome Type 4, Autosomal Dominant Ehlers Danlos Syndrome, Arterial Type Ehlers Danlos Syndrome, Ecchymotic Type Ehlers Danlos Syndrome, Sack Barabas Type Ehlers Danlos Syndrome, Sack-Barabas Type Ehlers-Danlos Syndrome, Arterial Type Ehlers-Danlos Syndrome, Ecchymotic Type Ehlers-Danlos Syndrome, Sack-Barabas Type Ehlers-Danlos Syndrome, Type IV, Autosomal Dominant Ehlers-Danlos Syndrome, Vascular Ehlers-Danlos Syndrome, Vascular Type Ehlers-Danlos Syndromes, Vascular Syndrome, Vascular Ehlers-Danlos Syndromes, 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 |
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Tree number(s): |
C14.907.055.448.250.256 C14.907.454.240.500 C15.378.463.515.240.500 C16.131.831.428.500 C16.320.850.260.500 C17.300.200.310.500 C17.800.804.428.500 C17.800.827.260.500 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000094623 | ||||||
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). |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Public MeSH Note: | 2023; use EHLERS-DANLOS SYNDROME 2008-2022 |
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History Note: | 2023; see EHLERS-DANLOS SYNDROME 2008-2022 |
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DeCS ID: | 60263 | ||||||
Unique ID: | D000094623 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 2023/01/01 | ||||||
Date of Entry: | 2022/07/08 | ||||||
Revision Date: | 2022/05/23 |
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Ehlers-Danlos Syndrome, Type IV
- Preferred
Concept UI |
M0501042 |
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). |
Preferred term | Ehlers-Danlos Syndrome, Type IV |
Entry term(s) |
EDS IV Ehlers Danlos Syndrome Type 4, Autosomal Dominant Ehlers Danlos Syndrome, Arterial Type Ehlers Danlos Syndrome, Ecchymotic Type Ehlers Danlos Syndrome, Sack Barabas Type Ehlers Danlos Syndrome, Sack-Barabas Type Ehlers-Danlos Syndrome, Arterial Type Ehlers-Danlos Syndrome, Ecchymotic Type Ehlers-Danlos Syndrome, Sack-Barabas Type Ehlers-Danlos Syndrome, Type IV, Autosomal Dominant Ehlers-Danlos Syndrome, Vascular Ehlers-Danlos Syndrome, Vascular Type Ehlers-Danlos Syndromes, Vascular Syndrome, Vascular Ehlers-Danlos Syndromes, 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 |
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