Tyrosinemia Rare Disorders Conditions and Diseases

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.

Top: Health: Conditions and Diseases: Rare Disorders: Tyrosinemia

See Also:

NORD: Tyrosinemia, Hereditary - Offers the synonyms, a general discussion and further resources.

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