Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3302721013 | Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302722018 | Spinocerebellar degeneration co-occurrent with macular corneal dystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302723011 | Spastic ataxia and corneal dystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3302724017 | Bedouin spastic ataxia syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3302725016 | Mousa-Al Din-Al Nassar syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400911017 | 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400912012 | A rare, hereditary ataxia disorder characterised 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. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder) | Is a | Macular corneal dystrophy | true | Inferred relationship | Some | ||
| Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder) | Is a | Spinocerebellar disease | true | Inferred relationship | Some | ||
| Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder) | Finding site | Spinal cord structure | true | Inferred relationship | Some | 2 | |
| Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
| Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 3 | |
| Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder) | Finding site | Structure of substantia propria of cornea | true | Inferred relationship | Some | 3 | |
| Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR