OMOP Concept 4284702
Epidermolysis bullosa simplex
StandardConditionSNOMED67144006Disorder
Maps from
12
Descendants
21
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
12 source codes normalize to Epidermolysis bullosa simplex via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141144 | Epidermolysis bullosa simplex | Non-standard |
| CIM10 | Q81.0 | Epidermolysis bullosa simplex | Non-standard |
| ICD10 | Q81.0 | Epidermolysis bullosa simplex | Non-standard |
| ICD10CM | Q81.0 | Epidermolysis bullosa simplex | Non-standard |
| ICD10CN | Q81.0 | Epidermolysis bullosa simplex | Non-standard |
| ICD10CN | Q81.000 | Epidermolysis bullosa simplex | Non-standard |
| ICD10GM | Q81.0 | Epidermolysis bullosa simplex | Non-standard |
| KCD7 | Q81.0 | Epidermolysis bullosa simplex | Non-standard |
| MeSH | D016110 | Epidermolysis Bullosa Simplex | Non-standard |
| Nebraska Lexicon | 67144006 | Epidermolysis bullosa simplex | Non-standard |
| Read | PH3y212 | Koebner's disease | Non-standard |
| Read | PH3y700 | Epidermolysis bullosa simplex | Non-standard |
Synonyms
Alternative names recorded for Epidermolysis bullosa simplex across source vocabularies.
- epidermólisis bullosa simple
- epidermólisis bullosa simple (trastorno)
- Epidermolysis bullosa simplex (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(27)Roll up to these when you need a wider cohort.
- 1Epidermolysis bullosa
- 2Degenerative skin disorder
- 2Developmental hereditary disorder
- 2Genodermatosis
- 2Hereditary disorder of the integument
- 3Congenital anomaly of skin
- 3Degenerative disorder
- 3Developmental disorder
- 3Disorder of integument
- 3Disorder of skin
- 3Hereditary disease
- 3Hereditary disorder by system
- 4Congenital anomaly of integument
- 4Disease
- 4Disorder of body system
- 4Disorder of skin and/or subcutaneous tissue
- 4Genetic disease
- 4Integumentary system finding
- 4Skin finding
- 5Clinical finding
- 5Congenital malformation
- 5Disorder involving the integument of fetus OR newborn
- 5Disorder of soft tissue
- 5General finding of soft tissue
- 5Skin AND/OR mucosa finding
Narrower concepts
(21)Included automatically when you query with descendants.
- 1Autosomal dominant epidermolysis bullosa simplex
- 1Autosomal recessive epidermolysis bullosa simplex
- 1Basal epidermolysis bullosa simplex
- 1Epidermolysis bullosa simplex herpetiformis
- 1Epidermolysis bullosa simplex with hypodontia
- 1Epidermolysis bullosa simplex with mottled pigmentation
- 1Epidermolysis simplex superficialis
- 1Generalized epidermolysis bullosa simplex
- 1Suprabasal epidermolysis bullosa simplex
- 2Epidermolysis bullosa simplex due to BP230 deficiency
- 2Epidermolysis bullosa simplex due to exophilin 5 deficiency
- 2Epidermolysis bullosa simplex due to plakophilin deficiency
- 2Epidermolysis bullosa simplex, Ogna type
- 2Epidermolysis bullosa simplex with circinate migratory erythema
- 2Epidermolysis bullosa simplex with muscular dystrophy
- 2Epidermolysis bullosa simplex with pyloric atresia
- 2Intermediate epidermolysis bullosa simplex with cardiomyopathy
- 2KRT14 related epidermolysis bullosa simplex
- 2Lethal acantholytic erosive disorder
- 2Lethal autosomal recessive epidermolysis bullosa simplex
- 2Weber-Cockayne syndrome
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