Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4945373017 | Amyotrophic lateral sclerosis type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4945374011 | ALS (amyotrophic lateral sclerosis) type 1 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4945375012 | Amyotrophic lateral sclerosis type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4945376013 | ALS1 - amyotrophic lateral sclerosis type 1 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4945382011 | A neurodegenerative disease with characteristics of progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord. Associated with mutations in the superoxide dismutase-1 gene (SOD1) on chromosome 21q22. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Amyotrophic lateral sclerosis type 1 | Is a | Chronic nervous system disorder (disorder) | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 1 | Is a | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 1 | Is a | Degenerative disorder | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 1 | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 1 | Is a | Amyotrophic lateral sclerosis | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 1 | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 | |
| Amyotrophic lateral sclerosis type 1 | Finding site | Structure of nervous system (body structure) | true | Inferred relationship | Some | 1 | |
| Amyotrophic lateral sclerosis type 1 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Autosomal recessive amyotrophic lateral sclerosis type 1 | Is a | True | Amyotrophic lateral sclerosis type 1 | Inferred relationship | Some | |
| Autosomal dominant amyotrophic lateral sclerosis type 1 | Is a | True | Amyotrophic lateral sclerosis type 1 | Inferred relationship | Some |
Reference Sets
FHIR