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Results 1 - 10 of 18 for mitochondrial hepatopathy
Did you mean mitochondrial "hepato pathy"?
  1. MEGDEL syndrome 
    ... I, Saada A, Sprecher E, Mandel H. Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3- ...
    https://medlineplus.gov/genetics/condition/megdel-syndrome - Genetics
  2. SERAC1 gene 
    ... I, Saada A, Sprecher E, Mandel H. Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3- ...
    https://medlineplus.gov/genetics/gene/serac1 - Genetics
  3. MPV17-related hepatocerebral mitochondrial DNA depletion syndrome 
    MPV17-related hepatocerebral mitochondrial DNA depletion syndrome is an inherited disorder that can cause liver disease and neurological problems. The signs and symptoms of this condition begin in infancy and typically include vomiting, diarrhea, and ...
    https://medlineplus.gov/...bral-mitochondrial-dna-depletion-syndrome - Genetics
  4. HADHA gene 
    ... Blish KR, Ibdah JA. Maternal heterozygosity for a mitochondrial trifunctional protein mutation as a cause for liver disease in pregnancy. Med Hypotheses. 2005;64(1):96- ...
    https://medlineplus.gov/genetics/gene/hadha - Genetics
  5. MPV17 gene 
    ... have been found to cause MPV17-related hepatocerebral mitochondrial DNA depletion syndrome, a condition characterized by liver disease and neurological problems that begin in infancy. Most ...
    https://medlineplus.gov/genetics/gene/mpv17 - Genetics
  6. Mitochondrial complex III deficiency 
    ... infancy but can appear later.The severity of mitochondrial complex III ... as liver disease that can lead to liver failure, kidney abnormalities ( ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  7. BCS1L gene 
    ... with this condition. More About This Health Condition ... (hepatopathy), kidneys (tubulopathy), and brain (encephalopathy). The BCS1L gene ...
    https://medlineplus.gov/genetics/gene/bcs1l - Genetics
  8. FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome 
    ... can have vision problems, hearing loss, liver abnormalities (hepatopathy), and immune deficiency due to a decrease in ... protein that is found within cell structures called mitochondria. Mitochondria are involved in a wide variety of ...
    https://medlineplus.gov/...thic-mitochondrial-dna-depletion-syndrome - Genetics
  9. Deoxyguanosine kinase deficiency 
    ... deficiency have the isolated hepatic form, which causes liver disease without serious neurological problems. The myopathic form is ... these infants typically begin to show signs of liver disease and brain dysfunction. Neurological signs and symptoms may ...
    https://medlineplus.gov/.../deoxyguanosine-kinase-deficiency - Genetics
  10. POLG gene 
    ... of mental and movement abilities (psychomotor regression), and liver disease. The liver disease in Alpers-Huttenlocher syndrome can be brought on ... in nerve function (neuropathy). The conditions previously named mitochondrial recessive ataxia syndrome (MIRAS) and sensory ataxia neuropathy ...
    https://medlineplus.gov/genetics/gene/polg - Genetics
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