Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3313730018 | Episodic ataxia type 7 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3313731019 | Episodic ataxia type 7 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 752551000241119 | ataxie épisodique type 7 (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 949981000172111 | ataxie épisodique type 7 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3313732014 | An exceedingly rare form of hereditary episodic ataxia with characteristics of ataxia with weakness, vertigo, and dysarthria without interictal findings. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Episodic ataxia type 7 (disorder) | est un(e) (attribut) | Episodic ataxia (disorder) | true | Inferred relationship | Some | ||
| Episodic ataxia type 7 (disorder) | localisation d'une constatation (attribut) | structure cérébelleuse | true | Inferred relationship | Some | 1 | |
| Episodic ataxia type 7 (disorder) | est un(e) (attribut) | Cerebellar ataxia | true | Inferred relationship | Some | ||
| Episodic ataxia type 7 (disorder) | est un(e) (attribut) | Hereditary disorder of nervous system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR