progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 3

Preferred Label : progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 3;

UMLS semantic type : T047 - Disease or Syndrome;

Détails

Origin ID

M0564047;

UMLS CUI

C1836439;

Automatic exact mappings (from CISMeF team)
- autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 [DO Concept]
Currated CISMeF NLP mapping
- Autosomal dominant progressive external ophthalmoplegia type 3 (disorder) [SNOMED CT concept]
- Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 3 [OMIM Phenotype]
- Progressive external ophthalmoplegia, autosomal dominant, type 3 [ICD-11 More detail]
Related record
- progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 3 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 3 [OMIM Phenotype]
- Progressive external ophthalmoplegia, autosomal dominant, type 3 [ICD-11 More detail]

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

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