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472316006: Hypertrophic mitochondrial cardiomyopathy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2951109019 Hypertrophic mitochondrial cardiomyopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2951132015 Hypertrophic mitochondrial cardiomyopathy en Synonym Active Entire term case insensitive SNOMED CT core module

10 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypertrophic mitochondrial cardiomyopathy Is a Hypertrophic cardiomyopathy false Inferred relationship Existential restriction modifier
Hypertrophic mitochondrial cardiomyopathy Is a Mitochondrial cardiomyopathy true Inferred relationship Existential restriction modifier
Hypertrophic mitochondrial cardiomyopathy Due to Mitochondrial cytopathy true Inferred relationship Existential restriction modifier 1
Hypertrophic mitochondrial cardiomyopathy Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier 2
Hypertrophic mitochondrial cardiomyopathy Finding site Myocardium structure true Inferred relationship Existential restriction modifier 2
Hypertrophic mitochondrial cardiomyopathy Is a Hypertrophic cardiomyopathy due to disorder true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Hypertrophic mitochondrial cardiomyopathy associated with cataracts and lactic acidosis Is a True Hypertrophic mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome Is a True Hypertrophic mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome Is a True Hypertrophic mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency Is a True Hypertrophic mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation Is a True Hypertrophic mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to mitochondrial transfer ribonucleic acid translation optimization 1 deficiency Is a True Hypertrophic mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Combined oxidative phosphorylation defect type 17 Is a True Hypertrophic mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome Is a True Hypertrophic mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome Is a True Hypertrophic mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier
Glutaminyl-transfer ribonucleic acid amidotransferase subunit-related combined oxidative phosphorylation defect Is a True Hypertrophic mitochondrial cardiomyopathy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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