Epidermolysis bullosa simplex (EBS) is a group of hereditary epidermolysis bullosa (HEB) disorders characterized by skin fragility resulting in intraepidermal blisters and erosions that occur either spontaneously or after physical trauma. [ Orphanet:304 ]

This is just here as a test because I lose it

Term information

database cross reference
  • DOID:4644 (MONDO:equivalentTo)
  • Orphanet:304 (MONDO:equivalentTo)
  • NCIT:C84692 (MONDO:equivalentTo)
  • ICD10:Q81.0 (Orphanet:304)
  • ICD9:757.39 (i2s)
  • GARD:0010752 (MONDO:equivalentTo)
  • UMLS:C0079298 (Orphanet:304)
  • MESH:D016110 (MONDO:equivalentTo)
  • SCTID:67144006 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_group_of_disorders

abbreviation
EBS [ Orphanet:304 ]

abbreviation
EEB [ Orphanet:304 ]

closeMatch

http://identifiers.org/snomedct/205585003

definition

Epidermolysis bullosa simplex (EBS) is a group of hereditary epidermolysis bullosa (HEB) disorders characterized by skin fragility resulting in intraepidermal blisters and erosions that occur either spontaneously or after physical trauma.

exactMatch

http://purl.obolibrary.org/obo/NCIT_C84692

http://www.orpha.net/ORDO/Orphanet_304

http://purl.obolibrary.org/obo/DOID_4644

http://linkedlifedata.com/resource/umls/id/C0079298

http://identifiers.org/mesh/D016110

http://identifiers.org/snomedct/67144006

has exact synonym

EEB

EBS

epidermolysis bullosa simplex

has related synonym

epidermolysis bullosa intraepidermic

id

MONDO:0017610

seeAlso

https://rarediseases.info.nih.gov/diseases/10752/epidermolysis-bullosa-simplex

Term relations