Directory of Tyrosinemia Resources

Home > Health > Conditions and Diseases > Nutritional and Metabolic Disorders > Inherited > Tyrosinemia

A rare genetic metabolic disorder characterized by lack of the enzyme fumarylacetoacetate hydrolase (FAH), which is needed to break down the amino acid tyrosine.

Resources in This Category

• NORD: Tyrosinemia, Hereditary

  http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Tyrosinemia,+Hereditary
  Offers the synonyms, a general discussion and further resources.

• Patient: Tyrosinaemia

  http://patient.info/doctor/tyrosinaemia
  Factsheet on this disorder of tyrosine metabolism, its description, epidemiology, presentation, differential diagnosis, investigations, associated diseases, management, complications, prognosis and prevention.

Related Categories

• Home > Health > Conditions and Diseases > Genetic Disorders
• Home > Health > Conditions and Diseases > Nutritional and Metabolic Disorders

 

Home > Health > Conditions and Diseases > Nutritional and Metabolic Disorders > Inherited > Tyrosinemia

 

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