corneal endothelial dystrophy 1

Preferred Label : corneal endothelial dystrophy 1;

Origin ID

C565156;

UMLS CUI

C3502718;

Currated CISMeF NLP mapping
- Congenital hereditary endothelial dystrophy type 1 (disorder) [SNOMED CT concept]
- Congenital hereditary endothelial dystrophy type I [ORDO Disease]
- Corneal endothelial dystrophy 1, autosomal dominant [OMIM Phenotype]
- congenital hereditary endothelial dystrophy type I [Disease (Nov.)]
MeSH term(s) associated for indexing
- corneal dystrophies, hereditary [MeSH Descriptor]
Record concept(s)
- corneal endothelial dystrophy 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]