Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3768467019 | Mills syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| 3768468012 | Mills syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3768469016 | A rare acquired motor neuron disease with characteristics of a slowly progressive unilateral ascending or descending hemiplegia, associated with unilateral or asymmetrical pyramidal signs and no sensory loss. It is a diagnosis of exclusion and controversy exists regarding whether the presence of bulbar symptoms, sphincter disturbances, fasciculations or cognitive manifestations are characteristics of the disease. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Mills syndrome | Is a | Motor neurone disease | true | Inferred relationship | Some | ||
| Mills syndrome | Finding site | Structure of nervous system | true | Inferred relationship | Some | 1 | |
| Mills syndrome | Occurrence | Period of life between birth and death | true | Inferred relationship | Some | 1 | |
| Mills syndrome | Is a | Chronic nervous system disorder | true | Inferred relationship | Some | ||
| Mills syndrome | Clinical course | Progressive | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR