malformation syndrome with skin/mucosae involvement junctional epidermolysis bullosa DOID:3209 EBJ GARD:0002152 JEB Junctional epidermolysis bullosa (JEB) is a form of inherited epidermolysis bullosa characterized by involvement of the skin and mucous membranes, and is defined by the formation of blistering lesions between the epidermis and the dermis at the lamina lucida level of the cutaneous basement membrane zone and by healing of lesions with atrophy and/or exuberant granulation tissue formation. MESH:D016109 MONDO:0017612 NCIT:C90598 Orphanet:305 SCTID:79855003 UMLS:C0079301 congenital junctional epidermolysis bullosa epidermolysis bullosa atrophicans epidermolysis bullosa hereditaria letalis epidermolysis bullosa, junctional https://rarediseases.info.nih.gov/diseases/2152/junctional-epidermolysis-bullosa inherited epidermolysis bullosa rare disease with odontological manifestation