Mitochondrial complex V (ATP synthase) deficiency, nuclear type 5 is a metabolic condition affecting multiple systems, particularly growth, muscular f...

Mitochondrial disease is an umbrella term for a group of disorders that affect how cells produce energy, often impacting multiple organ systems includ...

Mitochondrial DNA deletion syndrome with progressive myopathy is an extremely uncommon condition that primarily affects muscle function and eye moveme...

Mitochondrial DNA depletion syndrome is a clinically heterogeneous group of disorders characterized by a reduction in mitochondrial DNA copy number in...

Mitochondrial DNA depletion syndrome 1 is a multisystem disorder that primarily affects neuromuscular and gastrointestinal function. It is caused by p...

Mitochondrial DNA depletion syndrome 11 is a rare mitochondrial oxidative phosphorylation disorder that primarily affects skeletal muscle function and...

Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type) is an inherited condition that primarily affects the heart and skeletal muscles, with...

Mitochondrial DNA depletion syndrome 13 is a very rare disorder that affects the function of mitochondria, the energy-producing structures within cell...

Mitochondrial DNA depletion syndrome 20 (mngie type) is an inherited condition that affects multiple organ systems, particularly the nervous system an...

Mitochondrial DNA depletion syndrome 3 (hepatocerebral type) is a very rare condition caused by mutations in the DGUOK gene that affects mitochondrial...