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 |
| 4674063014 | Maternally inherited mitochondrial myopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4674064015 | Maternally inherited mitochondrial myopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Maternally inherited mitochondrial myopathy | Is a | Mitochondrial myopathy | true | Inferred relationship | Existential restriction modifier | ||
| Maternally inherited mitochondrial myopathy | Due to | Mitochondrial cytopathy | true | Inferred relationship | Existential restriction modifier | 2 | |
| Maternally inherited mitochondrial myopathy | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Maternally inherited mitochondrial myopathy | Is a | Maternally inherited mitochondrial deoxyribonucleic acid disease | true | Inferred relationship | Existential restriction modifier | ||
| Maternally inherited mitochondrial myopathy | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR