Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
100111010 | Macular corneal dystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
799190013 | Macular corneal dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
2206021000005114 | Makulær corneadystrofi | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital macular corneal dystrophy | Is a | True | Macular corneal dystrophy | Inferred relationship | Some | |
Macular corneal dystrophy Type I (disorder) | Is a | True | Macular corneal dystrophy | Inferred relationship | Some | |
Macular corneal dystrophy Type II (disorder) | Is a | True | Macular corneal dystrophy | Inferred relationship | Some | |
A rare, hereditary ataxia disorder characterized by the presence of spastic ataxia in association with bilateral congenital cataract, macular corneal dystrophy (stromal with deposition of mucoid material) and nonaxial myopia. Patients present normal intellectual development. There have been no further descriptions in the literature since 1986. | Is a | True | Macular corneal dystrophy | Inferred relationship | Some | |
Macular dystrophy of substantia propria of cornea of bilateral eyes (disorder) | Is a | True | Macular corneal dystrophy | Inferred relationship | Some |
This concept is not in any reference sets