OMOP Concept 4235741
Generalized epidermolysis bullosa simplex
StandardConditionSNOMED90496008Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Generalized epidermolysis bullosa simplex via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139540 | Generalised epidermolysis bullosa simplex | Non-standard |
| Nebraska Lexicon | 90496008 | Generalised epidermolysis bullosa simplex | Non-standard |
Synonyms
Alternative names recorded for Generalized epidermolysis bullosa simplex across source vocabularies.
- enfermedad de Kobner
- epidermólisis ampollar simple generalizada
- epidermólisis ampollar simple, tipo Kobner
- epidermólisis bullosa simple generalizada
- epidermólisis bullosa simple generalizada (trastorno)
- epidermólisis bullosa simple, tipo Kobner
- Epidermolysis bullosa simplex, Kobner type
- Generalised epidermolysis bullosa simplex
- Generalized epidermolysis bullosa simplex (disorder)
- Kobner disease
- Koebner epidermolysis bullosa
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(28)Roll up to these when you need a wider cohort.
- 1Epidermolysis bullosa simplex
- 2Epidermolysis bullosa
- 3Degenerative skin disorder
- 3Developmental hereditary disorder
- 3Genodermatosis
- 3Hereditary disorder of the integument
- 4Congenital anomaly of skin
- 4Degenerative disorder
- 4Developmental disorder
- 4Disorder of integument
- 4Disorder of skin
- 4Hereditary disease
- 4Hereditary disorder by system
- 5Congenital anomaly of integument
- 5Disease
- 5Disorder of body system
- 5Disorder of skin and/or subcutaneous tissue
- 5Genetic disease
- 5Integumentary system finding
- 5Skin finding
- 6Clinical finding
- 6Congenital malformation
- 6Disorder involving the integument of fetus OR newborn
- 6Disorder of soft tissue
- 6General finding of soft tissue
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