Ehlers-Danlos syndrome, classic type (cEDS) is a form of Ehlers-Danlos syndrome that affects the connective tissue and is characterized by skin hyperextensibility, widened atrophic scars and joint hypermobility. [ Orphanet : 287 ]

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0220679 (Orphanet:287)
  • Orphanet:287 (OMIM:130000)
  • SCTID:715318006 (MONDO:equivalentTo)
  • UMLS:C4225429 (MONDO:equivalentTo)
  • GARD:0002088 (MONDO:equivalentTo)
Subsets

ordo_disease

definition
  • Ehlers-Danlos syndrome, classic type (cEDS) is a form of Ehlers-Danlos syndrome that affects the connective tissue and is characterized by skin hyperextensibility, widened atrophic scars and joint hypermobility.
exactMatch
  • http://identifiers.org/snomedct/715318006
  • http://www.orpha.net/ORDO/Orphanet_287
  • http://linkedlifedata.com/resource/umls/id/C4225429
has exact synonym
  • Ehlers-Danlos syndrome classic type
  • EDS, classic type
  • Ehlers-Danlos syndrome, classic type
has related synonym
  • EDS II, formerly
  • EDS I, formerly
  • Ehlers Danlos syndrome, mild classic type, formerly
  • EDS II
  • Ehlers-Danlos syndrome, type I
  • Ehlers Danlos syndrome, mitis type
  • Ehlers-Danlos syndrome, gravis type, formerly
  • Ehlers-Danlos syndrome type 1 (formerly)
  • Ehlers-Danlos syndrome, type II, formerly
  • Ehlers-Danlos syndrome, severe classic type, formerly
  • classic Ehlers-Danlos syndrome
  • classical Ehlers-Danlos syndrome
  • Ehlers Danlos syndrome, mild classic type
  • Ehlers-Danlos syndrome, severe classic type
  • Ehlers-Danlos syndrome classical type
  • Ehlers-Danlos syndrome, type I, formerly
  • Ehlers-Danlos syndrome type 2
  • Ehlers Danlos syndrome, mitis type, formerly
  • Ehlers-Danlos syndrome type 2 (formerly)
  • EDS I
  • Ehlers-Danlos syndrome, type II
  • Ehlers-Danlos syndrome, gravis type
id
  • MONDO:0007522