Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3706577019 | Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3706578012 | Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Associated morphology | Primary atrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Is a | Hereditary optic atrophy | true | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Is a | Inherited optic neuropathy | false | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Is a | Chronic nervous system disorder | true | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Is a | Degenerative disease of the central nervous system | false | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Finding site | Optic nerve structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Occurrence | Childhood | false | Inferred relationship | Existential restriction modifier | 2 | |
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Finding site | Structure of central nervous system | false | Inferred relationship | Existential restriction modifier | 2 | |
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Occurrence | Childhood | true | Inferred relationship | Existential restriction modifier | 1 | |
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Is a | Hereditary ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Associated morphology | Degeneration | false | Inferred relationship | Existential restriction modifier | 2 | |
| Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR