Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2009. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 82938010 | Familial motor neuron disease | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 82939019 | Familial motor neuron disease, NOS | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 82940017 | Hereditary motor neuron disease, NOS | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 82941018 | Hereditary motor neuron disease | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 787510011 | Hereditary motor neuron disease (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary motor neuron disease | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary motor neuron disease | Is a | Familial disease | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary motor neuron disease | Is a | Motor neuron disease | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary motor neuron disease | Associated morphology | Degeneration | false | Inferred relationship | Existential restriction modifier | 2 | |
| Hereditary motor neuron disease | Finding site | Motor neuron | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary motor neuron disease | Finding site | Structure of nervous system | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Spinal muscular atrophy | Is a | True | Hereditary motor neuron disease | Inferred relationship | Existential restriction modifier | |
| Juvenile primary lateral sclerosis | Is a | True | Hereditary motor neuron disease | Inferred relationship | Existential restriction modifier | |
| Neurogenic scapuloperoneal syndrome Kaeser type | Is a | True | Hereditary motor neuron disease | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR