Condition

Mitochondrial disease

Related terms: Mitochondrial dysfunction, Mitochondrial disorders, Mitochondrial DNA disease

EstablishedTextbook physiology, or consistent findings reflected in national guidance.
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In brief

A group of metabolic disorders caused by gene changes that stop mitochondria, the structures that make energy in cells, from working properly.

  • Faults in how mitochondria work can cause symptoms in the muscles, the brain and sometimes the kidneys.

How it works

Mitochondria are small structures that produce energy in almost all of your cells. Mitochondrial diseases are a group of metabolic disorders caused by genetic mutations. Muscle and nerve cells have especially high energy needs, so muscle and nerve problems are common.

There are no cures for these diseases, but treatments may help with symptoms and slow the disease down. Mitochondrial DNA is generally inherited only from the mother.

Connections

2 connections on the map. Select a topic to read its page.

Mitochondrial disease can cause Muscle weakness and slow recoveryMuscle weaknessand slow recoveryMitochondrial disease is linked with Mitochondria (cell energy)Mitochondria (cell energy)Mitochondrial disease can cause Muscle weakness and slow recoveryMuscle weaknessand slow recoveryMitochondrial disease is linked with Mitochondria (cell energy)Mitochondria

Mitochondrial disease is linked with

Mitochondrial disease can cause

Sources

  1. Mitochondrial diseasesMedlinePlus (US National Library of Medicine), last reviewed 21 December 2025
  2. Mitochondria, Talking Glossary of Genomic and Genetic TermsNational Human Genome Research Institute (NIH), last reviewed 12 October 2026

Each connection above names its own source. See every source AskBioMap uses.

Summarised from MedlinePlus and the National Human Genome Research Institute. Sources read on 13 October 2026. General education only, not medical advice. Spotted a mistake? Please tell us through the HuBu-Intel contact page.

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