Dermatitis herpetiformis (DH) is a chronic autoimmune subepidermal bullous disease characterized by grouped pruritic lesions such as papules, urticarial plaques, erythema, and herpetiform vesiculae, with a predominantly symmetrical distribution on extensor surfaces of the elbows (90%), knees (30%), shoulders, buttocks, sacral region, and face of children and adults. Erosions, excoriations and hyperpigmentation usually follow. DH may also appear as a consequence of gluten intolerance. [ Orphanet:1656 ]

Synonyms: Durhing-Brocq disease Duhring's disease dermatosis herpetiformis dermatitis herpetiformis

This is just here as a test because I lose it

Term information

database cross reference
  • ICD10CM:L13.0 (Orphanet:1656/e)
  • MESH:D003874 (Orphanet:1656/e)
  • MedDRA:10012468 (Orphanet:1656/e)
  • UMLS:C0011608 (MONDO:equivalentTo)
  • icd11.foundation:286313127 (Orphanet:1656)
  • Wikipedia:Dermatitis_herpetiformis (EFO:1000684)
  • Orphanet:1656 (MONDO:equivalentTo)
  • EFO:1000684 (MONDO:equivalentTo)
  • DOID:8505 (MONDO:equivalentTo)
  • MEDGEN:8327 (MONDO:equivalentTo)
  • GARD:10075 (MONDO:GARD)
  • SCTID:111196000 (MONDO:equivalentTo)
  • NCIT:C26742 (MONDO:equivalentTo)
  • ICD9:694.0 (MONDO:i2s)
Subsets

ordo_disorder, gard_rare, otar, rare, orphanet_rare

closeMatch

http://identifiers.org/meddra/10012468

exactMatch

http://linkedlifedata.com/resource/umls/id/C0011608

http://www.orpha.net/ORDO/Orphanet_1656

http://identifiers.org/mesh/D003874

http://purl.obolibrary.org/obo/DOID_8505

http://purl.obolibrary.org/obo/NCIT_C26742

http://identifiers.org/snomedct/111196000

http://purl.bioontology.org/ontology/ICD10CM/L13.0

http://identifiers.org/medgen/8327

id

MONDO:0015614

Term relations