MeSH Browser

MeSH Supplementary: Ehlers-Danlos syndrome type 3
Unique ID: C536196
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536196
Entry Term(s): Benign hypermobility syndrome; Ehlers-Danlos Syndrome, Hypermobility Type; Ehlers-Danlos Syndrome, Type III
Registry Number: 0
Heading Mapped to: *Ehlers-Danlos Syndrome
Frequency: 121
Note: A hypermobility type of Ehlers-Danlos Syndrome (EDS), characterized by hyperxtensibility of the joints, recurrent joint dislocations, and the onset of OSTEOARTHRITIS in the fourth decade of life. MITRAL VALVE PROLAPSE may also be present. Skin abnormalities are less severe than in other forms of the EDS. Mutations in the COL3A1 and the TNXB genes have been identified. OMIM: 130020
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Ehlers-Danlos syndrome type 3 MeSH Supplementary Concept Data 2023