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Results 1 - 10 of 15 for Tyrosinemia
  1. Tyrosinemia is a genetic disorder characterized by problems breaking down the amino acid tyrosine, which is a building block of most proteins. If the condition is ...
  2. ... 86 FAH mutations have been found that cause tyrosinemia type I. This condition is characterized by severe ... problems and other features that are characteristic of tyrosinemia type I.In several cases of tyrosinemia type ...
  3. ... at least six HPD gene mutations that cause tyrosinemia type III. This condition is characterized by neurological ... death likely lead to the characteristic features of tyrosinemia type III. More About This Health Condition At ...
  4. ... TAT gene mutations have been found to cause tyrosinemia type II. This condition often affects the eyes, ... the skin, eye, and intellectual problems that characterize tyrosinemia type II. More About This Health Condition ATTY_ ...
  5. ... myeloma Ornithine transcarbamylase deficiency Osteomalacia Propionic acidemia Rickets Tyrosinemia type 1 Tyrosinemia type 2 Viral hepatitis Wilson ...
  6. Childhood Hepatocellular Carcinoma From the National Institutes of Health (National Cancer Institute)  
    Liver Cancer/Children ... Liver Cancer ... National Cancer Institute ... From the National Institutes of Health ... Childhood hepatocellular carcinoma is a rare type of childhood ...
  7. Amino Acid Metabolism Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Your digestive system breaks ...
  8. Liver Diseases (National Library of Medicine)  
    Your liver is the largest organ inside your body. It helps your body digest food, store energy, and remove poisons. There are many kinds of liver diseases: ...
  9. Newborn Screening (National Library of Medicine)  
    Your newborn infant has screening tests before leaving the hospital. There may be different tests depending on the state where you live. They include: Tests ...
  10. ... Foundation Turner Syndrome Society of the United States Tyrosinemia Society Unique (UK) United Leukodystrophy Foundation United Mitochondrial ...
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