OMOP Concept 4110106
Progressive recessive dystrophic epidermolysis bullosa
StandardConditionSNOMED254176007Disorder
Maps from
4
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
4 source codes normalize to Progressive recessive dystrophic epidermolysis bullosa via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139347 | Goldscheider's Disease | Non-standard |
| MeSH | C562637 | Epidermolysis Bullosa Dystrophica Neurotrophica | Non-standard |
| Nebraska Lexicon | 254176007 | Progressive recessive dystrophic epidermolysis bullosa | Non-standard |
| Read | PH3y211 | Goldscheider's disease | Non-standard |
Synonyms
Alternative names recorded for Progressive recessive dystrophic epidermolysis bullosa across source vocabularies.
- EBR 3
- enfermedad de Goldscheider
- epidermólisis bullosa distrófica recesiva progresiva
- epidermólisis bullosa distrófica recesiva progresiva (trastorno)
- Epidermolysis bullosa dystrophica neurotrophica
- Goldscheider disease
- Goldscheider's disease
- Progressive recessive dystrophic epidermolysis bullosa (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.
- 1Recessive dystrophic epidermolysis bullosa
- 2Autosomal recessive hereditary disorder
- 2Dystrophic epidermolysis bullosa
- 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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