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Jetskr9.net: Top: Health: Conditions and Diseases: Rare Disorders: Tyrosinemia (2)

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

See also:

NORD: Tyrosinemia, Hereditary - Offers the synonyms, a general discussion and further resources.
Tyrosinemia - For all people interested in connecting with others with this disease.

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Last update: 2008-11-30 21:51:41