progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 1

Preferred Label : progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 1;

MeSH synonym : progressive external ophthalmoplegia, autosomal dominant, 1;

Détails

Origin ID

C563575;

UMLS CUI

C1834846;

Automatic exact mappings (from CISMeF team)
- autosomal dominant progressive external ophthalmoplegia 1 [DO Concept]
Currated CISMeF NLP mapping
- Autosomal dominant progressive external ophthalmoplegia type 1 (disorder) [SNOMED CT concept]
- Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1 [OMIM Phenotype]
- Progressive external ophthalmoplegia, autosomal dominant, type 1 [ICD-11 More detail]
MeSH term(s) associated for indexing
- mitochondrial diseases [MeSH Descriptor]
- ophthalmoplegia [MeSH Descriptor]
Record concept(s)
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1 [OMIM Phenotype]
- Progressive external ophthalmoplegia, autosomal dominant, type 1 [ICD-11 More detail]

Position du mot-clé dans l'(les) arborescence(s) :

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