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Symptom Checker » Fatty liver » Oral lichen planus
 

Fatty liver and Oral lichen planus
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Fatty liver and Oral lichen planus

Fatty liver:

Oral lichen planus:

Results: Causes of Fatty liver AND Oral lichen planus

Note: Do not use for diagnosis; see limitations of results.

Results: 51 causes of Fatty liver OR Oral lichen planus

    1. 3-alpha-Hydroxyacyl-CoA Dehydrogenase Deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    2. 3-alpha-hydroxyacyl-coenzyme A dehydrogenase deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    3. Acute fatty liver of pregnancy
     A rare complication of pregnancy that can occur in the second half of the pregnancy. It is characterized by excessive fatty deposits in the liver which can be fatal without prompt diagnosis and treatment which involves delivering the baby as soon as possi...more »
    4. Acyl-CoA dehydrogenase, very long chain, deficiency of
     A rare inherited genetic condition where the body is unable to convert certain fats to energy i.e. there is not enough of a certain enzyme which is needed to metabolize a type of fat called long-chain fatty acids. The build-up of these fatty acids in the ...more »
    5. Autosomal dominant polycystic kidney disease
     Genetic kidney disease causing kidney cysts....more »
    6. Berardinelli-Seip congenital lipodystrophy
     A rare genetic disorder characterized by diabetes mellitus, loss of body fat, hepatomegaly, enlarged genitals, increased skeletal growth and other abnormalities....more »
    7. Berardinelli-Seip congenital lipodystrophy, type 1
     A rare genetic disorder characterized by early-onset diabetes mellitus, loss of body fat, serious insulin resistance, high blood triglycerides and fatty liver. Type 1 is distinguished from type 2 by the origin of the genetic defect. Type 1 is caused by a ...more »
    8. Berardinelli-Seip congenital lipodystrophy, type 2
     A rare genetic disorder characterized by early-onset diabetes mellitus, loss of body fat, serious insulin resistance, high blood triglycerides and fatty liver. Type 2 is distinguished from type 2 by the origin of the genetic defect. Type 2 is caused by a ...more »
    9. Biliary Atresia
     A rare condition that can affect newborns where the bile duct that carries the bile from the liver to the small intestine is blocked or missing....more »
    10. Chemical poisoning -- 1,1-Dimethylhydrazine
     1,1-Dimethylhydrazine is a chemical used mainly in jet fuel and rocket fuel, plant growth agent, photography and various other industrial uses. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms var...more »

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Notes About Causes

  • Warning - Beta version - information may be incorrect (details)
  • Disclaimer - Do not use this information for diagnosis (details)
  • Important - See your doctor - Only a doctor can give an accurate diagnosis (details)
 

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