acquired epidermolysis bullosa
Epidermolysis bullosa acquisita (EBA) is a subepidermal bullous dermatosis of autoimmune origin that was named as a result of its resemblance to hereditary forms of epidermolysis bullosa (HEB), most notably dystrophic HEB. [ Orphanet:46487 ]
Term info
- GARD:0006360 (MONDO:equivalentTo)
- ICD10CM:L12.3 (Orphanet:46487/e)
- UMLS:C0079293 (Orphanet:46487)
- NCIT:C84690 (MONDO:equivalentTo)
- MESH:D016107 (MONDO:equivalentTo)
- EFO:1000691 (MONDO:equivalentTo)
- DOID:4313 (MONDO:equivalentTo)
- MedDRA:10056508 (Orphanet:46487/e)
- Orphanet:46487 (MONDO:equivalentTo)
- SCTID:2772003 (MONDO:equivalentTo)
- ICD9:695.19 (MONDO:relatedTo)
gard_rare, ordo_disease
http://identifiers.org/meddra/10056508
Epidermolysis bullosa acquisita (EBA) is a subepidermal bullous dermatosis of autoimmune origin that was named as a result of its resemblance to hereditary forms of epidermolysis bullosa (HEB), most notably dystrophic HEB.
http://purl.obolibrary.org/obo/NCIT_C84690, http://identifiers.org/mesh/D016107, http://identifiers.org/snomedct/2772003, http://purl.obolibrary.org/obo/DOID_4313, http://purl.bioontology.org/ontology/ICD10CM/L12.3, http://linkedlifedata.com/resource/umls/id/C0079293, http://purl.obolibrary.org/obo/Orphanet_46487
epidermolysis bullosa Aquisita, epidermolysis bullosa acquisita, EBA, acquired epidermolysis bullosa
EB acquisita
MONDO:0018747
https://rarediseases.info.nih.gov/diseases/6360/epidermolysis-bullosa-acquisita