Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4634476017 | Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 4634477014 | MME-related autosomal dominant Charcot Marie Tooth disease type 2 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 4634478016 | Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4634479012 | MME-related autosomal dominant hereditary motor and sensory neuropathy type 2 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 | Is a | Autosomal dominant Charcot-Marie-Tooth disease type 2 | true | Inferred relationship | Existential restriction modifier | ||
| Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 | Is a | Chronic nervous system disorder | true | Inferred relationship | Existential restriction modifier | ||
| Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 | Is a | Peripheral nerve disease | true | Inferred relationship | Existential restriction modifier | ||
| Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 2 | |
| Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 | Finding site | Peripheral nerve structure | true | Inferred relationship | Existential restriction modifier | 3 | |
| Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 | Finding site | Nerve structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 | 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