| Descriptor English: | Ehlers-Danlos Syndrome | ||||||
| Descriptor Spanish: |
Síndrome de Ehlers-Danlos
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| Descriptor Portuguese: | Síndrome de Ehlers-Danlos | ||||||
| Descriptor French: | Syndrome d'Ehlers-Danlos | ||||||
| Entry term(s): |
Cutis Elastica Danlos Disease, Ehlers Disease, Ehlers Danlos Disease, Ehlers-Danlos EDS IV Ehlers Danlos Disease Ehlers Danlos Syndrome 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, Type IV Ehlers Danlos Syndrome, Vascular Type Ehlers-Danlos Disease Ehlers-Danlos Syndrome, Arterial Type Ehlers-Danlos Syndrome, Ecchymotic Type Ehlers-Danlos Syndrome, Sack-Barabas Type Ehlers-Danlos Syndrome, Type IV Ehlers-Danlos Syndrome, Type IV, Autosomal Dominant Ehlers-Danlos Syndrome, Vascular Type Syndrome, Ehlers-Danlos |
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| Tree number(s): |
C14.907.454.240 C15.378.463.515.240 C16.131.831.428 C16.320.850.260 C17.300.200.310 C17.800.804.428 C17.800.827.260 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D004535 | ||||||
| Scope note: | 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. |
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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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| Related: |
Reticulin
MeSH | ||||||
| DeCS ID: | 4605 | ||||||
| Unique ID: | D004535 | ||||||
| NLM Classification: | WR 218 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1966/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2015/06/22 |
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Ehlers-Danlos Syndrome
- Preferred
Ehlers-Danlos Syndrome, Type IV
- Narrower
| Concept UI |
M0007138 |
| Scope note | 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. |
| Preferred term | Ehlers-Danlos Syndrome |
| Entry term(s) |
Cutis Elastica Danlos Disease, Ehlers Disease, Ehlers Danlos Disease, Ehlers-Danlos Ehlers Danlos Disease Ehlers Danlos Syndrome Ehlers-Danlos Disease Syndrome, Ehlers-Danlos |
| Concept UI |
M0501042 |
| 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, Type IV Ehlers Danlos Syndrome, Vascular 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 Type |
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