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 |
3308175016 | Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3308176015 | Autosomal dominant Charcot-Marie-Tooth disease type 2C | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5401448014 | A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by the association of vocal cord anomalies, impairment of respiratory muscles and sensorineural hearing loss with the distal hands and feet weakness. Onset is between infancy and the 6th decade. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401449018 | A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterised by the association of vocal cord anomalies, impairment of respiratory muscles and sensorineural hearing loss with the distal hands and feet weakness. Onset is between infancy and the 6th decade. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) | Is a | Autosomal dominant hereditary disorder | false | Inferred relationship | Some | ||
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) | Is a | Charcot-Marie-Tooth disease, type II (disorder) | false | Inferred relationship | Some | ||
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) | Finding site | Peripheral nervous system structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 2 | |
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) | Finding site | Nerve structure | true | Inferred relationship | Some | 2 | |
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) | Is a | Autosomal dominant Charcot-Marie-Tooth disease type 2 | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)