Status: current, 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 |
| 4696772017 | Autosomal recessive amyotrophic lateral sclerosis type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4696773010 | Autosomal recessive amyotrophic lateral sclerosis type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4696774016 | ALS1 AR - amyotrophic lateral sclerosis type 1 autosomal recessive | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4696775015 | Autosomal recessive ALS (amyotrophic lateral sclerosis) type 1 | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 4945384012 | An autosomal recessive hereditary 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 |
| Autosomal recessive amyotrophic lateral sclerosis type 1 | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Autosomal recessive amyotrophic lateral sclerosis type 1 | évolution clinique (attribut) | progressif | true | Inferred relationship | Some | 2 | |
| Autosomal recessive amyotrophic lateral sclerosis type 1 | localisation d'une constatation (attribut) | système nerveux | true | Inferred relationship | Some | 1 | |
| Autosomal recessive amyotrophic lateral sclerosis type 1 | morphologie associée (attribut) | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
| Autosomal recessive amyotrophic lateral sclerosis type 1 | est un(e) (attribut) | Amyotrophic lateral sclerosis type 1 | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR