Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Oct 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4643781018 | PMP2-related Charcot-Marie-Tooth disease type 1 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 4643782013 | Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 4643783015 | Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4643786011 | PMP2-related Charcot-Marie-Tooth neuropathy type 1 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 4643787019 | PMP2-related hereditary motor and sensory neuropathy type 1 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 | Is a | Charcot-Marie-Tooth disease, type I | true | Inferred relationship | Existential restriction modifier | ||
| Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 | 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