OMOP Concept 4301401
Dystrophic epidermolysis bullosa inverse type
StandardConditionSNOMED403809003Disorder
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 Dystrophic epidermolysis bullosa inverse type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 403809003 | Dystrophic epidermolysis bullosa inverse type | Non-standard |
Synonyms
Alternative names recorded for Dystrophic epidermolysis bullosa inverse type across source vocabularies.
- Dystrophic epidermolysis bullosa inverse type (disorder)
- epidermólisis bullosa distrófica tipo inversa
- epidermólisis bullosa distrófica tipo inversa (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(29)Roll up to these when you need a wider cohort.
- 1Generalized dystrophic epidermolysis bullosa
- 2Dystrophic epidermolysis bullosa
- 3Epidermolysis bullosa
- 4Degenerative skin disorder
- 4Developmental hereditary disorder
- 4Genodermatosis
- 4Hereditary disorder of the integument
- 5Congenital anomaly of skin
- 5Degenerative disorder
- 5Developmental disorder
- 5Disorder of integument
- 5Disorder of skin
- 5Hereditary disease
- 5Hereditary disorder by system
- 6Congenital anomaly of integument
- 6Disease
- 6Disorder of body system
- 6Disorder of skin and/or subcutaneous tissue
- 6Genetic disease
- 6Integumentary system finding
- 6Skin finding
- 7Clinical finding
- 7Congenital malformation
- 7Disorder involving the integument of fetus OR newborn
- 7Disorder of soft tissue
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