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Mitochondrial disease
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Disorders caused by mitochondrial dysfunction
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Subclasses
5
Mitochondrial DNA depletion syndrome
Medical condition
Leigh syndrome
Metabolic disease
combined oxidative phosphorylation deficiency
Human disease
mitochondrial complex deficiency
human disease
Mitochondrial optic neuropathies
Group of visual disorders
Subject of
7
Systems Biology Approaches Toward Understanding Primary Mitochondrial Diseases
scientific article published on 01 February 2019
Mitochondrial disease and endocrine dysfunction
scientific article published on 7 October 2016
Mitochondrial DNA mutation analysis from exome sequencing-A more holistic approach in diagnostics of suspected mitochondrial disease
scientific article published on 11 June 2019
The utility of phenomics in diagnosis of inherited metabolic disorders
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing
scientific article
Mitochondrial complex deficiency by novel compound heterozygous variants and correlation with developmental delay, undescended testicle, and left ventricular noncompaction in a Japanese patient: A case report
scientific article published on 07 February 2019
Mitochondrial disease and epilepsy
scientific article published on 28 January 2012
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Mitochondrial disease is a group of genetic disorders caused by mitochondrial dysfunction. Mitochondria are the organelles that generate energy for the cell and are found in every cell of the human body except red blood cells. They convert the energy of food molecules into the ATP that powers most cell functions.

Instance of
developmental defect during embryogenesis
designated intractable/rare disease
class of disease
Subclass of
Inborn errors of metabolism
developmental anomaly of metabolic origin
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