Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 82938010 | Familial motor neuron disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 82939019 | Familial motor neuron disease, NOS | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 82940017 | Hereditary motor neuron disease, NOS | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 82941018 | Hereditary motor neuron disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary motor neuron disease (disorder) | localisation d'une constatation (attribut) | système nerveux | true | Inferred relationship | Some | 1 | |
| Hereditary motor neuron disease (disorder) | est un(e) (attribut) | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Hereditary motor neuron disease (disorder) | est un(e) (attribut) | Familial disease | false | Inferred relationship | Some | ||
| Hereditary motor neuron disease (disorder) | est un(e) (attribut) | maladie du motoneurone (trouble) | true | Inferred relationship | Some | ||
| Hereditary motor neuron disease (disorder) | morphologie associée (attribut) | dégénérescence | false | Inferred relationship | Some | 2 | |
| Hereditary motor neuron disease (disorder) | localisation d'une constatation (attribut) | Motor neuron | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Neurogenic scapuloperoneal syndrome Kaeser type (disorder) | est un(e) (attribut) | True | Hereditary motor neuron disease (disorder) | Inferred relationship | Some | |
| atrophie musculaire spinale (trouble) | est un(e) (attribut) | True | Hereditary motor neuron disease (disorder) | Inferred relationship | Some | |
| Juvenile primary lateral sclerosis (disorder) | est un(e) (attribut) | True | Hereditary motor neuron disease (disorder) | Inferred relationship | Some |
Reference Sets
FHIR