Inherited epidermolysis bullosa (EB) encompasses a number of disorders characterized by recurrent blister formation as the result of structural fragility within the skin and selected other tissues. [ Orphanet:79361 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10:Q81.2 (Orphanet:79361)
  • ICD10:Q81.1 (Orphanet:79361)
  • ICD10:Q81.9 (Orphanet:79361)
  • ICD10:Q81.8 (Orphanet:79361)
  • ICD9:757.39 (i2s)
  • ICD10:Q81.0 (Orphanet:79361)
  • SCTID:402781004 (MONDO:equivalentTo)
  • Orphanet:79361 (MONDO:equivalentTo)
Subsets

ordo_group_of_disorders

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml

definition

Inherited epidermolysis bullosa (EB) encompasses a number of disorders characterized by recurrent blister formation as the result of structural fragility within the skin and selected other tissues.

exactMatch

http://linkedlifedata.com/resource/umls/id/C1274224

http://identifiers.org/snomedct/402781004

http://www.orpha.net/ORDO/Orphanet_79361

has exact synonym

epidermolysis bullosa hereditaria

hereditary epidermolysis bullosa

id

MONDO:0019276