A genetic skin disorder caused by mutations in the type VII collagen gene (COL7A1). It is characterized by the formation of blisters and scarring in the skin and mucous membranes. [ NCIT:P378 ]
Synonyms: DEB dermolytic epidermolysis bullosa epidermolysis bullosa dystrophica
Term information
- SCTID:254185007 (MONDO:equivalentTo)
- NCIT:C84691 (MONDO:equivalentTo)
- ICD9:757.39 (MONDO:relatedTo)
- MESH:D016108 (MONDO:equivalentTo)
- DOID:4959 (MONDO:equivalentTo)
- Wikipedia:Epidermolysis_bullosa_dystrophica (EFO:1000692)
- GARD:2150 (Orphanet:303)
- EFO:1000692 (MONDO:equivalentTo)
- Orphanet:303 (MONDO:equivalentTo)
gard_rare, disease_grouping, rare, nord_rare, orphanet_rare, ordo_group_of_disorders
http://purl.obolibrary.org/obo/NCIT_C84691
http://identifiers.org/mesh/D016108
http://identifiers.org/snomedct/254185007
http://www.orpha.net/ORDO/Orphanet_303
http://purl.obolibrary.org/obo/DOID_4959