OMOP Concept 43021905
Hypertrophic mitochondrial cardiomyopathy
StandardConditionSNOMED472316006Disorder
Maps from
0
Descendants
10
Valid from
31 Jan 2013
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Hypertrophic mitochondrial cardiomyopathy across source vocabularies.
- Hypertrophic mitochondrial cardiomyopathy (disorder)
- miocardiopatía mitocondrial hipertrófica
- miocardiopatía mitocondrial hipertrófica (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(25)Roll up to these when you need a wider cohort.
- 1Hypertrophic cardiomyopathy due to disorder
- 1Mitochondrial cardiomyopathy
- 2Cardiac complication
- 2Cardiomyopathy associated with another disorder
- 2Hypertrophic cardiomyopathy
- 3Cardiomyopathy
- 3Heart disease
- 3Structural disorder of heart
- 4Cardiac finding
- 4Disorder of cardiovascular system
- 4Disorder of mediastinum
- 4Myocardial disease
- 5Cardiovascular finding
- 5Disorder of body system
- 5Disorder of thorax
- 5Mediastinal finding
- 5Myocardial finding
- 5Viscus structure finding
- 6Clinical finding
- 6Disease
- 6Disorder of thoracic segment of trunk
- 6Finding of region of thorax
- 7Disorder of trunk
- 7Finding of upper trunk
- 8Finding of trunk structure
Narrower concepts
(10)Included automatically when you query with descendants.
- 1Combined oxidative phosphorylation defect type 17
- 1Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
- 1Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome
- 1Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
- 1Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome
- 1Hypertrophic mitochondrial cardiomyopathy associated with cataracts and lactic acidosis
- 1Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
- 1Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
- 1Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome
- 1QRSL1-related combined oxidative phosphorylation defect
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