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Results 1 - 6 of 6 for Tyrosinemia
  1. Tyrosinemia 
    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 ...
    https://medlineplus.gov/genetics/condition/tyrosinemia - Genetics
  2. FAH gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/fah - Genetics
  3. HPD gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/hpd - Genetics
  4. TAT gene 
    ... 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_ ...
    https://medlineplus.gov/genetics/gene/tat - Genetics
  5. Where can I read more about the diseases and traits covered in my direct-to-consumer genetic testing report?: ... 
    ... cell anemia Sjögren-Larsson syndrome Tay-Sachs disease Tyrosinemia Usher syndrome Zellweger spectrum disorder , also called Zellweger ...
    https://medlineplus.gov/.../dtcgenetictesting/dtcghrpages - Genetics
  6. Hypermethioninemia 
    ... occur with other metabolic disorders, such as homocystinuria, tyrosinemia, and galactosemia, which also involve the faulty breakdown ...
    https://medlineplus.gov/genetics/condition/hypermethioninemia - Genetics