Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3312744015 | Juvenile amyotrophic lateral sclerosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3312745019 | Juvenile amyotrophic lateral sclerosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3312747010 | JALS - juvenile amyotrophic lateral sclerosis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401758014 | Juvenile amyotrophic lateral sclerosis (JALS) is a very rare severe motor neuron disease characterized by progressive upper and lower motor neuron degeneration causing facial spasticity, dysarthria, and gait disorders with onset before 25 years of age. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401759018 | Juvenile amyotrophic lateral sclerosis (JALS) is a very rare severe motor neuron disease characterised by progressive upper and lower motor neuron degeneration causing facial spasticity, dysarthria, and gait disorders with onset before 25 years of age. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Juvenile amyotrophic lateral sclerosis (disorder) | Is a | Amyotrophic lateral sclerosis | true | Inferred relationship | Some | ||
| Juvenile amyotrophic lateral sclerosis (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Juvenile amyotrophic lateral sclerosis (disorder) | Finding site | Structure of nervous system (body structure) | true | Inferred relationship | Some | 1 | |
| Juvenile amyotrophic lateral sclerosis (disorder) | Is a | Chronic nervous system disorder (disorder) | true | Inferred relationship | Some | ||
| Juvenile amyotrophic lateral sclerosis (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Juvenile amyotrophic lateral sclerosis (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Juvenile amyotrophic lateral sclerosis type 2 | Is a | True | Juvenile amyotrophic lateral sclerosis (disorder) | Inferred relationship | Some | |
| Juvenile amyotrophic lateral sclerosis type 5 | Is a | True | Juvenile amyotrophic lateral sclerosis (disorder) | Inferred relationship | Some |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR