Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2005. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital hereditary endothelial dystrophy (disorder) | Is a | Hereditary corneal dystrophy | true | Inferred relationship | Some | ||
Congenital hereditary endothelial dystrophy (disorder) | Is a | Anomaly of chromosome pair 20 | true | Inferred relationship | Some | ||
Congenital hereditary endothelial dystrophy (disorder) | Is a | Corneal endothelial dystrophy (disorder) | true | Inferred relationship | Some | ||
Congenital hereditary endothelial dystrophy (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
Congenital hereditary endothelial dystrophy (disorder) | Finding site | Chromosome pair 20 | false | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy (disorder) | Finding site | Corneal structure | false | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy (disorder) | Associated morphology | anomalie congénitale | false | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy (disorder) | Is a | Corneal degeneration (disorder) | false | Inferred relationship | Some | ||
Congenital hereditary endothelial dystrophy (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 2 | |
Congenital hereditary endothelial dystrophy (disorder) | Finding site | Structure of corneal endothelium | false | Inferred relationship | Some | 2 | |
Congenital hereditary endothelial dystrophy (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy (disorder) | Finding site | Structure of corneal endothelium | true | Inferred relationship | Some | 1 | |
Congenital hereditary endothelial dystrophy (disorder) | Associated morphology | anomalie congénitale | false | Inferred relationship | Some | ||
Congenital hereditary endothelial dystrophy (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Congenital hereditary endothelial dystrophy (disorder) | Finding site | Chromosome pair 20 | true | Inferred relationship | Some | 2 | |
Congenital hereditary endothelial dystrophy (disorder) | Associated morphology | Cellular AND/OR subcellular abnormality | true | Inferred relationship | Some | 2 | |
Congenital hereditary endothelial dystrophy (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Congenital hereditary endothelial dystrophy (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Congenital hereditary endothelial dystrophy (disorder) | Is a | Congenital malformation | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
dystrophie endothéliale congénitale héréditaire type I | Is a | False | Congenital hereditary endothelial dystrophy (disorder) | Inferred relationship | Some | |
Congenital hereditary endothelial dystrophy type 2 (disorder) | Is a | True | Congenital hereditary endothelial dystrophy (disorder) | Inferred relationship | Some | |
Corneal dystrophy-perceptive deafness (CDPD) or Harboyan syndrome is a degenerative corneal disorder characterized by the association of congenital hereditary endothelial dystrophy with progressive, postlingual sensorineural hearing loss. | Is a | True | Congenital hereditary endothelial dystrophy (disorder) | Inferred relationship | Some |
Reference Sets
Description inactivation indicator reference set