Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4168182019 | Congenital dystrophy of cornea (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4168183012 | Congenital corneal dystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4168184018 | Congenital dystrophy of cornea | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital dystrophy of cornea | Is a | Congenital anomaly of cornea | true | Inferred relationship | Existential restriction modifier | ||
| Congenital dystrophy of cornea | Is a | Corneal dystrophy | true | Inferred relationship | Existential restriction modifier | ||
| Congenital dystrophy of cornea | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital dystrophy of cornea | Finding site | Corneal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital dystrophy of cornea | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital dystrophy of cornea | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Francois syndrome | Is a | True | Congenital dystrophy of cornea | Inferred relationship | Existential restriction modifier | |
| Stern Lubinsky Durrie syndrome | Is a | True | Congenital dystrophy of cornea | Inferred relationship | Existential restriction modifier | |
| Ophthalmomandibulomelic dysplasia | Is a | True | Congenital dystrophy of cornea | Inferred relationship | Existential restriction modifier | |
| Congenital macular corneal dystrophy | Is a | True | Congenital dystrophy of cornea | Inferred relationship | Existential restriction modifier | |
| Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome | Is a | True | Congenital dystrophy of cornea | Inferred relationship | Existential restriction modifier | |
| Congenital hereditary endothelial dystrophy and perceptive deafness syndrome | Is a | True | Congenital dystrophy of cornea | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets