DMOZ Internet Directory : Health : Conditions_and_Diseases : Nutritional_and_Metabolic

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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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NORD: Tyrosinemia, Hereditary - Offers the synonyms, a general discussion and further resources. Patient: Tyrosinaemia - Factsheet on this disorder of tyrosine metabolism, its description, epidemiology, presentation, differential diagnosis, investigations, associated diseases, management, complications, prognosis and prevention.

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