OMOP Concept 4220198
Epidermolysis bullosa simplex, Ogna type
StandardConditionSNOMED398071000Disorder
Maps from
3
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Epidermolysis bullosa simplex, Ogna type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141141 | Epidermolysis bullosa simplex, ogna type | Non-standard |
| MeSH | C535962 | Epidermolysis bullosa simplex, Ogna type | Non-standard |
| Nebraska Lexicon | 398071000 | Epidermolysis bullosa simplex, Ogna type | Non-standard |
Synonyms
Alternative names recorded for Epidermolysis bullosa simplex, Ogna type across source vocabularies.
- epidermólisis bullosa simple tipo Ogna
- epidermólisis bullosa simple tipo Ogna (trastorno)
- Epidermolysis bullosa simplex of Ogna
- Epidermolysis bullosa simplex, Ogna type (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(31)Roll up to these when you need a wider cohort.
- 1Autosomal dominant epidermolysis bullosa simplex
- 2Autosomal dominant hereditary disorder
- 2Epidermolysis bullosa simplex
- 3Autosomal hereditary disorder
- 3Epidermolysis bullosa
- 4Degenerative skin disorder
- 4Developmental hereditary disorder
- 4Genodermatosis
- 4Hereditary disease
- 4Hereditary disorder of the integument
- 5Congenital anomaly of skin
- 5Degenerative disorder
- 5Developmental disorder
- 5Disorder of integument
- 5Disorder of skin
- 5Genetic disease
- 5Hereditary disorder by system
- 6Congenital anomaly of integument
- 6Disease
- 6Disorder of body system
- 6Disorder of skin and/or subcutaneous tissue
- 6Integumentary system finding
- 6Skin finding
- 7Clinical finding
- 7Congenital malformation
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