Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4953815019 | Amyotrophic lateral sclerosis type 7 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 4953816018 | Amyotrophic lateral sclerosis type 7 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4953817010 | ALS7 - amyotrophic lateral sclerosis type 7 | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 4953818017 | 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. Cytogenetic location is 20p13. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Amyotrophic lateral sclerosis type 7 | Is a | Degenerative disorder | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 7 | Is a | Genetic disease | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 7 | Is a | Amyotrophic lateral sclerosis | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 7 | Finding site | Structure of nervous system | true | Inferred relationship | Some | 1 | |
| Amyotrophic lateral sclerosis type 7 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
| Amyotrophic lateral sclerosis type 7 | Is a | Chronic nervous system disorder | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 7 | Clinical course | Progressive | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR