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  2. Mitochondrial disease - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_disease

    Mitochondrial disease is a group of disorders caused by mitochondrial ... Example of a pedigree for a genetic trait inherited by mitochondrial DNA in animals and ...

  3. Human mitochondrial genetics - Wikipedia

    en.wikipedia.org/wiki/Human_mitochondrial_genetics

    Because mitochondrial diseases (diseases due to malfunction of mitochondria) can be inherited both maternally and through chromosomal inheritance, the way in which they are passed on from generation to generation can vary greatly depending on the disease. Mitochondrial genetic mutations that occur in the nuclear DNA can occur in any of the ...

  4. Category:Mitochondrial diseases - Wikipedia

    en.wikipedia.org/.../Category:Mitochondrial_diseases

    Pages in category "Mitochondrial diseases" The following 25 pages are in this category, out of 25 total. This list may not reflect recent changes. ...

  5. Mitochondrial neurogastrointestinal encephalopathy syndrome ...

    en.wikipedia.org/wiki/Mitochondrial_neuro...

    Mitochondrial neurogastrointestinal encephalopathy syndrome (MNGIE) is a rare autosomal recessive mitochondrial disease. [2] It has been previously referred to as polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudoobstruction (POLIP syndrome). [3] The disease presents in childhood, but often goes unnoticed for decades.

  6. Mitochondrial DNA depletion syndrome - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_DNA...

    Mitochondrial DNA depletion syndrome (MDS or MDDS), or Alper's disease, is any of a group of autosomal recessive disorders that cause a significant drop in mitochondrial DNA in affected tissues. Symptoms can be any combination of myopathic , hepatopathic , or encephalomyopathic . [ 1 ]

  7. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.

  8. Genetic disorder - Wikipedia

    en.wikipedia.org/wiki/Genetic_disorder

    Genetic disorder; Diagram featuring examples of a disease located on each chromosome ... A genetic disorder is a ... as the mitochondria are mostly developed by non ...

  9. Mitochondrial myopathy - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_myopathy

    Mitochondrial myopathy literally means mitochondrial muscle disease, muscle disease caused by mitochondrial dysfunction. The mitochondrion is the primary producer of energy in nearly all cells throughout the body. The exception is mature erythrocytes (red blood cells), so that they do not use up the oxygen that they carry.