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 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Autosomal recessive amyotrophic lateral sclerosis type 1 | est un(e) (attribut) | True | Amyotrophic lateral sclerosis type 1 | Inferred relationship | Some | |
| Autosomal dominant amyotrophic lateral sclerosis type 1 | est un(e) (attribut) | True | Amyotrophic lateral sclerosis type 1 | Inferred relationship | Some |
This concept is not in any reference sets
FHIR