Epidermolysis bullosa dystrophica, Pasini type

Preferred Label : Epidermolysis bullosa dystrophica, Pasini type;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0530417;

UMLS CUI

C0432322;

Automatic exact mappings (from CISMeF team)
- Dominant dystrophic epidermolysis bullosa, albopapular type (disorder) [SNOMED CT concept]
- Epidermolysis bullosa dystrophica, autosomal dominant [OMIM Phenotype]
Related record
- epidermolysis bullosa dystrophica, pasini type [MeSH Supplementary Concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant dystrophic epidermolysis bullosa, Pasini type [ORDO Disease]
- Autosomal dominant generalized dystrophic epidermolysis bullosa [ORDO Disease]
- Dominant dystrophic epidermolysis bullosa, albopapular type (disorder) [SNOMED CT concept]
- Epidermolysis bullosa dystrophica, autosomal dominant [OMIM Phenotype]
- dominant dystrophic epidermolysis bullosa, albopapular type [SNOMED Notion]