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 |
| 3310403014 | Infantile striatonigral degeneration (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3310404015 | Infantile striatonigral degeneration | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3311374010 | Infantile bilateral striatal necrosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3311375011 | Comprises of several syndromes of bilateral symmetric spongy degeneration of the caudate nucleus, putamen and globus pallidus with characteristics of developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. Can be familial or sporadic. The familial form has an insidious onset and a slowly progressive downhill course, while the sporadic form is associated with abrupt neurologic dysfunction following an acute systemic febrile illness such as a mycoplasma, measles or streptococcus infection. Familial disease can be inherited as an autosomal recessive or mitochondrial disorder. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Infantile striatonigral degeneration (disorder) | Is a | Striatonigral degeneration | true | Inferred relationship | Some | ||
| Infantile striatonigral degeneration (disorder) | Associated morphology | Degeneration | false | Inferred relationship | Some | 1 | |
| Infantile striatonigral degeneration (disorder) | Occurrence | Infancy | true | Inferred relationship | Some | 1 | |
| Infantile striatonigral degeneration (disorder) | Finding site | Structure of nigrostriate fiber (body structure) | true | Inferred relationship | Some | 1 | |
| Infantile striatonigral degeneration (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
| Infantile striatonigral degeneration (disorder) | Interprets | Movement | true | Inferred relationship | Some | 3 | |
| Infantile striatonigral degeneration (disorder) | Has interpretation | Slow | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Sporadic infantile bilateral striatal necrosis | Is a | True | Infantile striatonigral degeneration (disorder) | Inferred relationship | Some | |
| Familial infantile bilateral striatal necrosis | Is a | True | Infantile striatonigral degeneration (disorder) | Inferred relationship | Some |
Reference Sets
Description inactivation indicator reference set
FHIR