Status: current, Sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4696763013 | Autosomal dominant amyotrophic lateral sclerosis type 1 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4696764019 | Autosomal dominant ALS (amyotrophic lateral sclerosis) type 1 | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4696766017 | Autosomal dominant amyotrophic lateral sclerosis type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4696771012 | ALS1 AD - amyotrophic lateral sclerosis type 1 autosomal dominant | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant amyotrophic lateral sclerosis type 1 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant amyotrophic lateral sclerosis type 1 | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal dominant amyotrophic lateral sclerosis type 1 | Finding site | Structure of nervous system | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal dominant amyotrophic lateral sclerosis type 1 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal dominant amyotrophic lateral sclerosis type 1 | Is a | Amyotrophic lateral sclerosis type 1 | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR