Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
359707011 | Mitochondrial cytopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
629193019 | Mitochondrial cytopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
2871257019 | Mitochondrial disease | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Mitochondrial cytopathy | Is a | Metabolic myopathy | false | Inferred relationship | Existential restriction modifier | ||
Mitochondrial cytopathy | Finding site | Skeletal muscle structure | false | Inferred relationship | Existential restriction modifier | ||
Mitochondrial cytopathy | Is a | Metabolic disease | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Tryptophanyl tRNA synthetase 2, mitochondrial-related combined oxidative phosphorylation defect | Is a | True | Mitochondrial cytopathy | Inferred relationship | Existential restriction modifier | |
Syndromic sensorineural deafness due to combined oxidative phosphorylation defect | Is a | True | Mitochondrial cytopathy | Inferred relationship | Existential restriction modifier | |
[X]Mitochondrial myopathy, not elsewhere classified | Is a | False | Mitochondrial cytopathy | Inferred relationship | Existential restriction modifier | |
No family history of mitochondrial cytopathy | Associated finding | True | Mitochondrial cytopathy | Inferred relationship | Existential restriction modifier | 1 |
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This concept is not in any reference sets