OMOP Concept 4297656
Epidermolysis bullosa acquisita, Brunsting-Perry type
StandardConditionSNOMED402450009Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Epidermolysis bullosa acquisita, Brunsting-Perry type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 402450009 | Epidermolysis bullosa acquisita, Brunsting-Perry type | Non-standard |
Synonyms
Alternative names recorded for Epidermolysis bullosa acquisita, Brunsting-Perry type across source vocabularies.
- epidermólisis bullosa adquirida, tipo Brunsting-Perry
- epidermólisis bullosa adquirida, tipo Brunsting-Perry (trastorno)
- Epidermolysis bullosa acquisita, Brunsting-Perry type (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Acquired epidermolysis bullosa
- 2Autoimmune skin disease
- 2Blister of skin
- 2Chronic disease of immune function
- 2Chronic disease of skin
- 2Degenerative skin disorder
- 2Epidermal fragility
- 3Autoimmune disease
- 3Blister
- 3Chronic disease
- 3Degenerative disorder
- 3Disorder of immune function
- 3Disorder of skin
- 3Fragile skin
- 3Injury of integument
- 3Injury of soft tissue
- 3Skin lesion
- 4Disease
- 4Disorder of integument
- 4Disorder of skin and/or subcutaneous tissue
- 4Disorder of soft tissue
- 4Lesion of skin and/or skin-associated mucous membrane
- 4Lesion of soft tissue
- 4Skin finding
- 4Skin or mucosa lesion
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