Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4168182019 | Congenital dystrophy of cornea (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4168183012 | Congenital corneal dystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4168184018 | Congenital dystrophy of cornea | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital dystrophy of cornea (disorder) | est un(e) (attribut) | Congenital anomaly of cornea | true | Inferred relationship | Some | ||
| Congenital dystrophy of cornea (disorder) | est un(e) (attribut) | Corneal dystrophy | true | Inferred relationship | Some | ||
| Congenital dystrophy of cornea (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Congenital dystrophy of cornea (disorder) | localisation d'une constatation (attribut) | cornée (structure corporelle) | true | Inferred relationship | Some | 1 | |
| Congenital dystrophy of cornea (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Congenital dystrophy of cornea (disorder) | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| syndrome de François | est un(e) (attribut) | True | Congenital dystrophy of cornea (disorder) | Inferred relationship | Some | |
| Stern Lubinsky Durrie syndrome (disorder) | est un(e) (attribut) | True | Congenital dystrophy of cornea (disorder) | Inferred relationship | Some | |
| Ophthalmomandibulomelic dysplasia (disorder) | est un(e) (attribut) | True | Congenital dystrophy of cornea (disorder) | Inferred relationship | Some | |
| Congenital macular corneal dystrophy | est un(e) (attribut) | True | Congenital dystrophy of cornea (disorder) | Inferred relationship | Some | |
| Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome | est un(e) (attribut) | True | Congenital dystrophy of cornea (disorder) | Inferred relationship | Some | |
| Congenital hereditary endothelial dystrophy and perceptive deafness syndrome (disorder) | est un(e) (attribut) | True | Congenital dystrophy of cornea (disorder) | Inferred relationship | Some |
This concept is not in any reference sets