Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4592709012 | Maternally inherited mitochondrial disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4592761012 | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4592762017 | Maternally inherited mitochondrial deoxyribonucleic acid disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4592835016 | Maternally inherited mtDNA (mitochondrial deoxyribonucleic acid) disorder | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | Is a | Hereditary disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Maternally inherited mitochondrial dystonia (disorder) | Is a | True | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | Inferred relationship | Some | |
| Maternally inherited mitochondrial cardiomyopathy and myopathy | Is a | False | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | Inferred relationship | Some | |
| Maternally inherited Leigh syndrome (disorder) | Is a | True | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | Inferred relationship | Some | |
| Leber's optic atrophy | Is a | True | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | Inferred relationship | Some | |
| Myoclonic epilepsy with ragged red fibers | Is a | True | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | Inferred relationship | Some | |
| Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia (disorder) | Is a | True | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | Inferred relationship | Some | |
| Maternally inherited mitochondrial myopathy (disorder) | Is a | True | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | Inferred relationship | Some | |
| Maternally inherited mitochondrial cardiomyopathy (disorder) | Is a | True | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | Inferred relationship | Some | |
| Maternally inherited diabetes and deafness (disorder) | Is a | True | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | Inferred relationship | Some | |
| Neurogenic muscle weakness, ataxia and retinitis pigmentosa (disorder) | Is a | True | Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) | Inferred relationship | Some |
Reference Sets
FHIR