Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 787510011 | Hereditary motor neuron disease (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 82938010 | Familial motor neuron disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 82939019 | Familial motor neuron disease, NOS | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 82940017 | Hereditary motor neuron disease, NOS | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| 82941018 | Hereditary motor neuron disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary motor neuron disease | Finding site | Structure of nervous system | true | Inferred relationship | Some | 1 | |
| Hereditary motor neuron disease | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Hereditary motor neuron disease | Is a | Familial disease | false | Inferred relationship | Some | ||
| Hereditary motor neuron disease | Is a | Motor neurone disease | true | Inferred relationship | Some | ||
| Hereditary motor neuron disease | Associated morphology | Degeneration | false | Inferred relationship | Some | 2 | |
| Hereditary motor neuron disease | Finding site | Motor neuron | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Neurogenic scapuloperoneal syndrome Kaeser type | Is a | True | Hereditary motor neuron disease | Inferred relationship | Some | |
| Spinal muscular atrophy | Is a | True | Hereditary motor neuron disease | Inferred relationship | Some | |
| Juvenile primary lateral sclerosis | Is a | True | Hereditary motor neuron disease | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR