Tyrosinemia Rare Disorders Conditions and Diseases
A rare genetic metabolic disorder characterized by lack of the enzyme fumarylacetoacetate hydrolase (FAH), which is needed to break down the amino acid tyrosine.
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Tyrosinemia
See Also:
- Top/Health/Conditions and Diseases/Genetic Disorders
- Top/Health/Conditions and Diseases/Nutrition and Metabolism Disorders
- NORD: Tyrosinemia, Hereditary - Offers the synonyms, a general discussion and further rare disorders resources.
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