Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3701703015 | Distal hereditary motor neuropathy type 1 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3701704014 | Distal hereditary motor neuropathy type 1 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3701705010 | Autosomal dominant distal juvenile spinal muscular atrophy type 1 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3701706011 | A rare neuromuscular disease with characteristics of slowly progressive lower limb muscular weakness and atrophy, without sensory impairment. Additional clinical features may include pes cavus, hammertoe and increased muscle tone. | 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