Next Generation Sequencing Competence Network

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.

Descriptor ID	D004535
MeSH 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
Concept/Terms	Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome Ehlers Danlos Syndrome Syndrome, Ehlers-Danlos Cutis Elastica Ehlers Danlos Disease Danlos Disease, Ehlers Disease, Ehlers Danlos Ehlers-Danlos Disease Disease, Ehlers-Danlos Ehlers-Danlos Syndrome, Type IV Ehlers-Danlos Syndrome, Type IV Ehlers Danlos Syndrome, Type IV 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, Sack Barabas Type Ehlers-Danlos Syndrome, Type IV, Autosomal Dominant Ehlers Danlos Syndrome Type 4, Autosomal Dominant Ehlers Danlos Syndrome, Arterial Type Ehlers Danlos Syndrome, Ecchymotic Type Ehlers-Danlos Syndrome, Vascular Type Ehlers Danlos Syndrome, Vascular Type EDS IV

Below are MeSH descriptors whose meaning is more general than "Ehlers-Danlos Syndrome".

Below are MeSH descriptors whose meaning is related to "Ehlers-Danlos Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Ehlers-Danlos Syndrome".