junctional epidermolysis bullosa
skin condition characterized by blister formation within the lamina lucida of the basement membrane zone
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junctional epidermolysis bullosa
Summary
junctional epidermolysis bullosa is a developmental defect during embryogenesis[1].
Key Facts
- junctional epidermolysis bullosa's instance of is recorded as developmental defect during embryogenesis[2].
- junctional epidermolysis bullosa's instance of is recorded as class of disease[3].
- junctional epidermolysis bullosa is a type of epidermolysis bullosa[4].
- junctional epidermolysis bullosa is a type of malformation syndrome with skin/mucosae involvement[5].
- junctional epidermolysis bullosa is a type of inherited epidermolysis bullosa[6].
- junctional epidermolysis bullosa is a type of rare disease with odontological manifestation[7].
- junctional epidermolysis bullosa's NCI Thesaurus ID is recorded as C90598[8].
- junctional epidermolysis bullosa's health specialty is recorded as medical genetics[9].
- junctional epidermolysis bullosa's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3209[10].
- junctional epidermolysis bullosa's exact match is recorded as http://identifiers.org/doid/DOID:3209[11].
- junctional epidermolysis bullosa's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_305[12].
- junctional epidermolysis bullosa's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].