epidermolysis bullosa, nos

Preferred Label : epidermolysis bullosa, nos;

Details

Origin ID

D6-90900;

UMLS CUI

C0014527;

Currated CISMeF NLP mapping
- Acquired epidermolysis bullosa [MedDRA Preferred Term]
- Epidermolysis Bullosa [NCIt concept]
- Epidermolysis bullosa [PASCAL descriptor]
- Epidermolysis bullosa [ICD-10 category]
- Epidermolysis bullosa [MedDRA Preferred Term]
- Epidermolysis bullosa [ICD-10 category (who)]
- Epidermolysis bullosa (disorder) [SNOMED CT concept]
- Epidermolysis bullosa, unspecified [ICD-10 Sub-category]
- Epidermolysis bullosa, unspecified [ICD-10 Sub-category (who)]
- Inherited epidermolysis bullosa [ORDO Disease]
- epidermolysis bullosa [MeSH Descriptor]
- epidermolysis bullosa [MeSH concept]
ICD-10 exact mapping(s)
- Epidermolysis bullosa, unspecified [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Kindler epidermolysis bullosa [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Epidermal disease [ORDO Disease]
- Genetic epidermal disorder [ORDO Disease]
- Genodermatosis with ocular features [ORDO Disease]
Metaterm(s)
- metabolism [CISMeF Metaterm]
Référence SNOMED
- blister, nos [SNOMED Notion]
- epidermis [SNOMED Notion]
- separation, nos [SNOMED Notion]
SNOMED CT concept
- Epidermolysis bullosa (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Epidermolysis Bullosa [NCIt concept]
- Epidermolysis bullosa [ICD-10 category]
- Epidermolysis bullosa [MedDRA Preferred Term]
- Epidermolysis bullosa [ICD-10 category (who)]
- Epidermolysis bullosa [PASCAL descriptor]
- Epidermolysis bullosa (disorder) [SNOMED CT concept]
- Epidermolysis bullosa, unspecified [ICD-10 Sub-category]
- Epidermolysis bullosa, unspecified [ICD-10 Sub-category (who)]
- epidermolysis bullosa [MeSH Descriptor]
- epidermolysis bullosa [MeSH concept]
- epidermolysis bullosa [Disease (Nov.)]
- epidermolysis bullosa [DO Concept]

Keyword's position in hierarchy(ies) :

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