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Results 1 - 5 of 5 for Tyrosinemia type I
  1. Tyrosinemia 
    ... tyrosinemia, distinguished by their symptoms and genetic cause. Tyrosinemia type I is the most severe form of this ... increased tendency to bleed (particularly nosebleeds). In addition, tyrosinemia type I can lead to liver and kidney failure, ...
    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 liver ... problems and other features that are characteristic of tyrosinemia type I.In several cases of tyrosinemia type I, ...
    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 problems ... death likely lead to the characteristic features of tyrosinemia type III. More About This Health Condition At least ...
    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, skin, ... the skin, eye, and intellectual problems that characterize tyrosinemia type II. More About This Health Condition ATTY_HUMAN ...
    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?: ... 
    ... called MCAD deficiency Maple syrup urine disease Mucolipidosis type IV ... Usher syndrome Zellweger spectrum disorder , also called Zellweger ...
    https://medlineplus.gov/.../dtcgenetictesting/dtcghrpages - Genetics