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240096000: Mitochondrial cytopathy (disorder)

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
359706019 Mitochondrial myopathy en Synonym Inactive Only initial character case insensitive SNOMED CT core 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

123 descendants. Search Descendants:

Expanded Value Set

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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