dermatitis herpetiformis
http://purl.obolibrary.org/obo/MONDO_0015614
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 ]
Term info
- NCIT:C26742 (MONDO:equivalentTo)
- Wikipedia:Dermatitis_herpetiformis (EFO:1000684)
- UMLS:C0011608 (Orphanet:1656/e)
- Orphanet:1656 (MONDO:equivalentTo)
- EFO:1000684 (MONDO:equivalentTo)
- MESH:D003874 (Orphanet:1656/e)
- SCTID:111196000 (MONDO:equivalentTo)
- ICD10CM:L13.0 (Orphanet:1656/e)
- DOID:8505 (MONDO:equivalentTo)
- ICD9:694.0 (MONDO:i2s)
- MedDRA:10012468 (Orphanet:1656/e)
ordo_disease
http://identifiers.org/meddra/10012468
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.
http://linkedlifedata.com/resource/umls/id/C0011608, http://identifiers.org/mesh/D003874, http://purl.obolibrary.org/obo/DOID_8505, http://purl.obolibrary.org/obo/Orphanet_1656, http://purl.obolibrary.org/obo/NCIT_C26742, http://identifiers.org/snomedct/111196000, http://purl.bioontology.org/ontology/ICD10CM/L13.0
Durhing-Brocq disease, Duhring's disease, dermatosis herpetiformis, dermatitis herpetiformis
MONDO:0015614