Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4670032016 | Autosomal recessive axonal Charcot-Marie-Tooth disease type 2T | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4670033014 | Charcot-Marie-Tooth disease type 2T (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| 4670034015 | Charcot-Marie-Tooth disease type 2T | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Charcot-Marie-Tooth disease type 2T | Is a | Autosomal recessive Charcot-Marie-Tooth disease type 2 | true | Inferred relationship | Existential restriction modifier | ||
| Charcot-Marie-Tooth disease type 2T | Finding site | Peripheral nervous system structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Charcot-Marie-Tooth disease type 2T | Finding site | Nerve structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Charcot-Marie-Tooth disease type 2T | Associated morphology | Atrophy | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR