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472315005: Mitochondrial cardiomyopathy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2013. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2951123017 Mitochondrial cardiomyopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2951138016 Mitochondrial cardiomyopathy en Synonym Active Entire term case insensitive SNOMED CT core module


18 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mitochondrial cardiomyopathy Is a Cardiomyopathy associated with another disorder true Inferred relationship Existential restriction modifier
Mitochondrial cardiomyopathy Finding site Myocardium structure true Inferred relationship Existential restriction modifier 2
Mitochondrial cardiomyopathy Due to Mitochondrial cytopathy true Inferred relationship Existential restriction modifier 1
Mitochondrial cardiomyopathy Is a Cardiac complication true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Hypertrophic mitochondrial cardiomyopathy Is a True Mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Histiocytoid mitochondrial cardiomyopathy Is a True Mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Fatal infantile mitochondrial cardiomyopathy Is a True Mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Maternally inherited mitochondrial cardiomyopathy and myopathy Is a True Mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Dilated cardiomyopathy due to mitochondrial disease Is a True Mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome Is a True Mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Combined oxidative phosphorylation defect type 23 Is a True Mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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