dystrophic epidermolysis bullosa pruriginosa
Dystrophic epidermolysis bullosa pruriginosa is a rare subtype of dystrophic epidermolysis bullosa (DEB, see this term) characterized by generalized or localized skin lesions associated with severe, if not intractable, pruritus
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dystrophic epidermolysis bullosa pruriginosa
Summary
dystrophic epidermolysis bullosa pruriginosa is a developmental defect during embryogenesis[1].
Key Facts
- dystrophic epidermolysis bullosa pruriginosa's instance of is recorded as developmental defect during embryogenesis[2].
- dystrophic epidermolysis bullosa pruriginosa's instance of is recorded as rare disease[3].
- dystrophic epidermolysis bullosa pruriginosa's instance of is recorded as class of disease[4].
- dystrophic epidermolysis bullosa pruriginosa is a type of epidermolysis bullosa dystrophica[5].
- dystrophic epidermolysis bullosa pruriginosa's ICD-9-CM is recorded as 757.39[6].
- dystrophic epidermolysis bullosa pruriginosa's genetic association is recorded as COL7A1[7].
- dystrophic epidermolysis bullosa pruriginosa's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_89843[8].