Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4674391010 | Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 4674392015 | Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect | Is a | Hereditary motor and sensory neuropathy | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect | Is a | Disorder of copper metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect | Due to | Disorder of copper metabolism | true | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect | Finding site | Peripheral nervous system structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR