Epidermolysis bullosa letalis

Preferred Label : Epidermolysis bullosa letalis;

Inclusion CIM-10 : Herlitz' syndrome;

Rare : true;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q811;

UMLS CUI

C0079683;

Automatic exact mappings (from CISMeF team)
- Epidermolysis bullosa hereditaria letalis [PASCAL descriptor]
- congenital junctional epidermolysis bullosa [SNOMED Notion]
- epidermolysis bullosa, junctional [MeSH Descriptor]
Currated CISMeF NLP mapping
- Epidermolysis bullosa letalis [ICD-10 Sub-category (who)]
- Epidermolysis bullosa, junctional 1b, severe [OMIM Phenotype]
- Junctional epidermolysis bullosa gravis of Herlitz (disorder) [SNOMED CT concept]
- Junctional epidermolysis bullosa, generalised severe [ICD-11 More detail]
- Severe generalized junctional epidermolysis bullosa [ORDO Disease]
- epidermolysis bullosa letalis [MeSH concept]
- junctional epidermolysis bullosa Herlitz type [DO Concept]
DO Cross reference
- junctional epidermolysis bullosa Herlitz type [DO Concept]
Orphanet concepts
- Inherited epidermolysis bullosa [ORDO Disease]
- Severe generalized junctional epidermolysis bullosa [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Epidermolysis bullosa, junctional 1b, severe [OMIM Phenotype]
- Junctional epidermolysis bullosa gravis of Herlitz (disorder) [SNOMED CT concept]
- Severe generalized junctional epidermolysis bullosa [ORDO Disease]
- epidermolysis bullosa letalis [MeSH concept]
- junctional epidermolysis bullosa Herlitz type [DO Concept]

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