Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3308187011 | Autosomal dominant Charcot-Marie-Tooth disease type 2J (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3308188018 | Autosomal dominant Charcot-Marie-Tooth disease type 2J | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3308189014 | A form of axonal Charcot-Marie-Tooth disease a peripheral sensorimotor neuropathy. Relatively late onset papillary abnormalities and deafness in most patients associated with distal weakness and muscle atrophy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3868181000052119 | autosomalt dominant Charcot-Marie-Tooths sjukdom typ 2J | sv | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant Charcot-Marie-Tooth disease type 2J (disorder) | Is a | Autosomal dominant hereditary disorder | false | Inferred relationship | Some | ||
Autosomal dominant Charcot-Marie-Tooth disease type 2J (disorder) | Is a | Charcot-Marie-Tooth disease, type II (disorder) | false | Inferred relationship | Some | ||
Autosomal dominant Charcot-Marie-Tooth disease type 2J (disorder) | Finding site | Peripheral nervous system structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant Charcot-Marie-Tooth disease type 2J (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 2 | |
Autosomal dominant Charcot-Marie-Tooth disease type 2J (disorder) | Finding site | Nerve structure | true | Inferred relationship | Some | 2 | |
Autosomal dominant Charcot-Marie-Tooth disease type 2J (disorder) | Is a | Autosomal dominant Charcot-Marie-Tooth disease type 2 | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets