corneal endothelial dystrophy type 2

Preferred Label : corneal endothelial dystrophy type 2;

MeSH synonym : corneal dystrophy, congenital hereditary endothelial; maumenee corneal dystrophy; congenital hereditary endothelial dystrophy of the cornea; corneal endothelial dystrophy 2; CHED2 Congenital hereditary endothelial dystrophy of the cornea 2;

Details

Origin ID

C536439;

UMLS CUI

C1857569;

Automatic exact mappings (from CISMeF team)
- posterior polymorphous corneal dystrophy 1 [DO Concept]
Currated CISMeF NLP mapping
- Congenital hereditary endothelial dystrophy type 2 (disorder) [SNOMED CT concept]
- Congenital hereditary endothelial dystrophy type II [ORDO Disease]
- Corneal endothelial dystrophy [OMIM Phenotype]
- congenital hereditary endothelial dystrophy of cornea [DO Concept]
- congenital hereditary endothelial dystrophy type II [Disease (Nov.)]
MeSH term(s) associated for indexing
- corneal dystrophies, hereditary [MeSH Descriptor]
- fuchs' endothelial dystrophy [MeSH Descriptor]
Record concept(s)
- Corneal endothelial dystrophy type 2 [MeSH concept]
See also inter- (CISMeF)
- Corneal dystrophy, posterior polymorphous, 1 [OMIM Phenotype]
- Corneal endothelial dystrophy 1, autosomal dominant [OMIM Phenotype]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital hereditary endothelial dystrophy type 2 (disorder) [SNOMED CT concept]
- Congenital hereditary endothelial dystrophy type II [ORDO Disease]
- Corneal endothelial dystrophy [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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