Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4953512014 | Amyotrophic lateral sclerosis type 6 | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4953513016 | ALS6 - amyotrophic lateral sclerosis type 6 | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 4953514010 | Amyotrophic lateral sclerosis type 6 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 4953517015 | 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. Caused by heterozygous mutation in the FUS gene on chromosome 16p11. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Amyotrophic lateral sclerosis type 6 | Is a | Chronic nervous system disorder | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 6 | Is a | Degenerative disorder | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 6 | Is a | Genetic disease | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 6 | Is a | Amyotrophic lateral sclerosis | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 6 | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
| Amyotrophic lateral sclerosis type 6 | Finding site | Structure of nervous system | true | Inferred relationship | Some | 1 | |
| Amyotrophic lateral sclerosis type 6 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR