epidermolysis bullosa

Preferred Label : epidermolysis bullosa;

UMLS semantic type : T019 - Congenital Abnormality; T047 - Disease or Syndrome;

Details

Origin ID

M0007557;

UMLS CUI

C0014527;

Automatic exact mappings (from CISMeF team)
- Inherited epidermolysis bullosa (disorder) [Inactive SNOMED CT concept]
- Other epidermolysis bullosa [ICD-10 Sub-category (who)]
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 [ICD-10 category (who)]
- Epidermolysis bullosa [MedDRA Preferred Term]
- Epidermolysis bullosa (disorder) [SNOMED CT concept]
- Epidermolysis bullosa, unspecified [ICD-10 Sub-category (who)]
- Epidermolysis bullosa, unspecified [ICD-10 Sub-category]
- Inherited epidermolysis bullosa [ORDO Disease]
- epidermolysis bullosa [DO Concept]
- epidermolysis bullosa [Disease (Nov.)]
- epidermolysis bullosa, nos [SNOMED Notion]
Related record
- epidermolysis bullosa [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Epidermolysis Bullosa [NCIt concept]
- Epidermolysis bullosa [ICD-10 category]
- Epidermolysis bullosa [ICD-10 category (who)]
- Epidermolysis bullosa [MedDRA Preferred Term]
- 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 [DO Concept]
- epidermolysis bullosa [Disease (Nov.)]
- epidermolysis bullosa, nos [SNOMED Notion]

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