Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4964309016 | ALS10 - amyotrophic lateral sclerosis type 10 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4964310014 | Amyotrophic lateral sclerosis type 10 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4964311013 | Amyotrophic lateral sclerosis type 10 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4964314017 | 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. There is evidence this disease is caused by heterozygous mutation in the TARDBP gene that encodes the TDP43 protein on chromosome 1p36. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Amyotrophic lateral sclerosis type 10 (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 10 (disorder) | Is a | Chronic nervous system disorder (disorder) | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 10 (disorder) | Is a | Degenerative disorder | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 10 (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 10 (disorder) | Is a | Amyotrophic lateral sclerosis | true | Inferred relationship | Some | ||
| Amyotrophic lateral sclerosis type 10 (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 | |
| Amyotrophic lateral sclerosis type 10 (disorder) | Finding site | Structure of nervous system (body structure) | true | Inferred relationship | Some | 1 | |
| Amyotrophic lateral sclerosis type 10 (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set
FHIR