OMOP Concept 43020666
Mitochondrial cardiomyopathy
StandardConditionSNOMED472315005Disorder
Maps from
0
Descendants
19
Valid from
31 Jan 2013
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Mitochondrial cardiomyopathy across source vocabularies.
- miocardiopatía mitocondrial
- miocardiopatía mitocondrial (trastorno)
- Mitochondrial cardiomyopathy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Cardiac complication
- 1Cardiomyopathy associated with another disorder
- 2Cardiomyopathy
- 2Heart disease
- 3Cardiac finding
- 3Disorder of cardiovascular system
- 3Disorder of mediastinum
- 3Myocardial disease
- 4Cardiovascular finding
- 4Disorder of body system
- 4Disorder of thorax
- 4Mediastinal finding
- 4Myocardial finding
- 4Viscus structure finding
- 5Clinical finding
- 5Disease
- 5Disorder of thoracic segment of trunk
- 5Finding of region of thorax
- 6Disorder of trunk
- 6Finding of upper trunk
- 7Finding of trunk structure
Narrower concepts
(19)Included automatically when you query with descendants.
- 1Combined oxidative phosphorylation defect type 23
- 1Dilated cardiomyopathy due to mitochondrial disease
- 1Fatal infantile mitochondrial cardiomyopathy
- 1Histiocytoid mitochondrial cardiomyopathy
- 1Hypertrophic mitochondrial cardiomyopathy
- 1Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome
- 1Maternally inherited mitochondrial cardiomyopathy
- 2Combined oxidative phosphorylation defect type 17
- 2Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
- 2Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome
- 2Histiocytoid mitochondrial cardiomyopathy due to cytochrome aa3 deficiency
- 2Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
- 2Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome
- 2Hypertrophic mitochondrial cardiomyopathy associated with cataracts and lactic acidosis
- 2Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
- 2Maternally inherited mitochondrial cardiomyopathy and myopathy
- 2Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
- 2Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome
- 2QRSL1-related combined oxidative phosphorylation defect
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