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Results 1 - 10 of 28 for hepatopathy
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  1. ... an increased risk of developing non-alcoholic fatty liver disease (NAFLD). NAFLD is a buildup of excessive fat ... also been associated with the worsening of other liver diseases, such as a viral infection called hepatitis C. ...
  2. ... her liver. In very rare cases of maternal liver disease, the mother has one copy of an altered ... role of the mother's HADHA mutation in liver disease is unclear. ECHA_HUMAN GBP hydroxyacyl dehydrogenase, subunit ...
  3. ... been found to cause a severe form of liver disease called progressive familial intrahepatic cholestasis type 2 (PFIC2). PFIC2 is a disorder that causes progressive liver disease, which often leads to liver failure. To develop ...
  4. ... been found to cause a severe form of liver disease called progressive familial intrahepatic cholestasis type 3 (PFIC3). ... often appear in early childhood. PFIC3 causes progressive liver disease, which often leads to liver failure. Affected individuals ...
  5. ... a person's risk of developing lung disease, liver disease, and other abnormalities.Many SERPINA1 gene variants change ... Mahadeva R, Lomas DA. Alpha(1)-antitrypsin deficiency, liver disease and emphysema. Int J Biochem Cell Biol. 2003 ...
  6. ... blood cells (polycythemia); and liver abnormalities, including irreversible liver disease (cirrhosis).Mutations in the SLC30A10 gene impair the ... parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease. Am J Hum Genet. 2012 Mar 9;90( ...
  7. ... of mental and movement abilities (psychomotor regression), and liver disease. The liver disease in Alpers-Huttenlocher syndrome can be brought on ...
  8. ... been found to cause a severe form of liver disease called progressive familial intrahepatic cholestasis type 1 (PFIC1). ... in liver cells, damaging these cells and causing liver disease. Although the ATP8B1 protein is found throughout the ...
  9. ... neurological problems and can include nephronophthisis, eye abnormalities, liver disease, and other abnormalities. As in nephronophthisis type1 (described ...
  10. ... copies of the CPT1A gene develop this maternal liver disease. Little is known about the relationship between CPT1A ...
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