Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3763685016 | Amyotrophic lateral sclerosis type 4 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3763686015 | ALS4 - amyotrophic lateral sclerosis type 4 | en | Synonym | Active | Case sensitive | SNOMED CT core |
3763687012 | dHMN (distal hereditary motor neuropathy) with upper motor neuron signs | en | Synonym | Active | Case sensitive | SNOMED CT core |
3763688019 | Amyotrophic lateral sclerosis type 4 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3763689010 | A rare genetic motor neuron disease with characteristics of late childhood or adolescent onset of slowly progressive severe distal limb muscle weakness and wasting, in association with pyramidal signs, normal sensation and absence of bulbar involvement. Leads to degeneration of motor neurons in the brain and spinal cord. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set