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Results 1 - 10 of 90 for Abnormality of the mitochondrion
  1. Parkinson's Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Parkinson's Disease/Start Here ... Parkinson's Disease ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Parkinson’s ...
    https://www.ninds.nih.gov/.../disorders/parkinsons-disease - External Health Links
  2. Mitochondrial neurogastrointestinal encephalopathy disease 
    ... These genetic changes impair the normal function of mitochondria. Although mtDNA abnormalities underlie the digestive and neurological problems characteristic of ...
    https://medlineplus.gov/...rogastrointestinal-encephalopathy-disease - Genetics
  3. TYMP gene 
    ... These genetic changes impair the normal function of mitochondria. Although mtDNA abnormalities underlie the digestive and neurological problems that are ...
    https://medlineplus.gov/genetics/gene/tymp - Genetics
  4. MT-ND1 gene 
    ... of complex I, which disrupts energy production within mitochondria. Although these abnormalities have the greatest impact on tissues that require ...
    https://medlineplus.gov/genetics/gene/mt-nd1 - Genetics
  5. MT-ND5 gene 
    ... of complex I, which disrupts energy production within mitochondria. Although these abnormalities have the greatest impact on tissues that require ...
    https://medlineplus.gov/genetics/gene/mt-nd5 - Genetics
  6. Mitochondrial DNA 
    ... loss of intellectual functions (dementia), hearing loss, and abnormalities involving the eyes and vision.Most of the body's cells contain thousands of mitochondria, each with one or more copies of mitochondrial ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  7. LETM1 gene 
    ... loss of this gene alters the structure of mitochondria; however, it is unclear how this abnormality is related to the signs and symptoms of ...
    https://medlineplus.gov/genetics/gene/letm1 - Genetics
  8. MMADHC gene 
    ... developmental delay, eye defects, neurological problems, and blood abnormalities. The MMADHC gene variants that cause this condition result in the production of a protein that cannot transport vitamin B12 to either the mitochondria or the cytoplasm, which disrupts production of both ...
    https://medlineplus.gov/genetics/gene/mmadhc - Genetics
  9. HARS2 gene 
    ... in males and females with the disorder and abnormalities of the ovaries in affected ... speculate that impaired protein assembly disrupts mitochondrial ...
    https://medlineplus.gov/genetics/gene/hars2 - Genetics
  10. LARS2 gene 
    ... hearing loss in affected males and females and abnormalities of the ovaries in ... speculate that impaired protein assembly disrupts mitochondrial ...
    https://medlineplus.gov/genetics/gene/lars2 - Genetics
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