OMOP Concept 4246290
Epidermolysis bullosa
StandardConditionSNOMED61003004Disorder
Maps from
26
Descendants
59
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
26 source codes normalize to Epidermolysis bullosa via the OMOP "Maps to" relationship.
Showing 25 of 26 source codes. Retrieve the full set via the API.
Synonyms
Alternative names recorded for Epidermolysis bullosa across source vocabularies.
- Acantholysis bullosa
- Acanthosis bullosa
- acantólisis bullosa
- Bullous recurrent eruption
- dermatitis bullosa hereditaria
- Dermatitis bullosa hereditaria
- EB - Epidermolysis bullosa
- enfermedad de Fox
- epidermólisis bullosa
- epidermólisis bullosa (trastorno)
- Epidermolysis bullosa (disorder)
- erupción recurrente bullosa
- Fox disease
- Keratolysis bullosa hereditaria
- queratólisis bullosa hereditaria
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(26)Roll up to these when you need a wider cohort.
- 1Degenerative skin disorder
- 1Developmental hereditary disorder
- 1Genodermatosis
- 1Hereditary disorder of the integument
- 2Congenital anomaly of skin
- 2Degenerative disorder
- 2Developmental disorder
- 2Disorder of integument
- 2Disorder of skin
- 2Hereditary disease
- 2Hereditary disorder by system
- 3Congenital anomaly of integument
- 3Disease
- 3Disorder of body system
- 3Disorder of skin and/or subcutaneous tissue
- 3Genetic disease
- 3Integumentary system finding
- 3Skin finding
- 4Clinical finding
- 4Congenital malformation
- 4Disorder of soft tissue
- 4Fetal and/or neonatal disorder of integument
- 4General finding of soft tissue
- 4Skin AND/OR mucosa finding
- 5Congenital disease
Showing 25 of 26. Retrieve the full set via the API.
Narrower concepts
(59)Included automatically when you query with descendants.
- 1Dystrophic epidermolysis bullosa
- 1Epidermolysis bullosa simplex
- 1Junctional epidermolysis bullosa
- 1Kindler epidermolysis bullosa
- 2Autosomal dominant epidermolysis bullosa simplex
- 2Autosomal recessive epidermolysis bullosa simplex
- 2Basal epidermolysis bullosa simplex
- 2Congenital junctional epidermolysis bullosa
- 2Epidermolysis bullosa simplex herpetiformis
- 2Epidermolysis bullosa simplex with hypodontia
- 2Epidermolysis bullosa simplex with mottled pigmentation
- 2Epidermolysis simplex superficialis
- 2Generalized dystrophic epidermolysis bullosa
- 2Generalized epidermolysis bullosa simplex
- 2Generalized junctional epidermolysis bullosa
- 2Junctional epidermolysis bullosa non-Herlitz type
- 2Late-onset junctional epidermolysis bullosa
- 2Localized dystrophic epidermolysis bullosa
- 2Localized junctional epidermolysis bullosa
- 2Recessive dystrophic epidermolysis bullosa
- 2Suprabasal epidermolysis bullosa simplex
- 3Acral dystrophic epidermolysis bullosa
- 3Autosomal dominant generalized dystrophic epidermolysis bullosa
- 3Centripetalis recessive dystrophic epidermolysis bullosa
- 3Cicatricial junctional epidermolysis bullosa
Showing 25 of 59. Retrieve the full set via the API.
Get this concept via the API
Resolve Epidermolysis bullosa - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/4246290?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card