A rare genetic metabolic disorder characterized by lack of the enzyme fumarylacetoacetate hydrolase (FAH), which is needed to break down the amino acid tyrosine....
This page was last updated on October 2nd, 2008
This page was last updated on October 2nd, 2008
Tyrosinemia (from Rare Disorders)
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NORD: Tyrosinemia, Hereditary
Offers the synonyms, a general discussion and further resources.
National Library of Medicine
The synonyms of Tyrosinemia 11, a summary and major features.
Tyrosinemia
For all people interested in connecting with others with this disease.
Offers the synonyms, a general discussion and further resources.
The synonyms of Tyrosinemia 11, a summary and major features.
For all people interested in connecting with others with this disease.
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