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22 results
  1. ... disorder. Learn more about the gene associated with Carnitine-acylcarnitine translocase deficiency SLC25A20 Inheritance This condition is inherited in an ...
  2. ... other tissues. Health Conditions Related to Genetic Changes Carnitine-acylcarnitine translocase deficiency At least 27 mutations in the SLC25A20 gene ...
  3. ... published></health-condition-summary><health-condition-summary ><name >Carnitine-acylcarnitine translocase deficiency</name><ghr-page >https://medlineplus.gov/genetics/condition/ ...
  4. ... Leukoencephalopathy with vanishing white matter CACT deficiency, see Carnitine-acylcarnitine translocase deficiency CADASIL, see Cerebral autosomal dominant arteriopathy with subcortical ...
  5. ... topic><topic ><url >https://medlineplus.gov/genetics/condition/carnitine-acylcarnitine-translocase-deficiency</url><title >Carnitine-acylcarnitine translocase deficiency</title><other_ ...
  6. ... Profound nonketotic hypoglycemia mimics other FAO defects. SLC25A20 Carnitine-acylcarnitine translocase deficiency (OMIM 212138 ) AR AR = autosomal recessive ; FAO = fatty ...
  7. Lipids include fats, oils, and cholesterol. Disorders like Gaucher disease and Tay-Sachs cause problems with how your body uses lipids. Read more. ... Metabolism is ...
  8. Mitochondria make energy for your cells. Diseases can affect mitochondria, often causing nerve and muscle problems. Find out more. ... Metabolism is the process your ...
  9. Your newborn infant has screening tests before leaving the hospital. Get the facts about these tests and what you should expect. ... Your newborn infant has screening ...
  10. ... 20320. Citation on PubMed Ramsay RR, Zammit VA. Carnitine ... II deficiency: a clinical, biochemical, and molecular review. Lab Invest. ...
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