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Tyrosinemia: A rare genetic metabolic disorder characterized by a deficiency of particular enzymes which prevents the breakdown of tyrosine which then builds up in the liver. More detailed information about the symptoms, causes, and treatments of Tyrosinemia is available below.
See full list of 26 symptoms of Tyrosinemia
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Read more about Deaths and Tyrosinemia.
Review possible medical complications related to Tyrosinemia:
Read more about causes of Tyrosinemia.
Research the causes of these diseases that are similar to, or related to, Tyrosinemia:
Read more about symptoms of Tyrosinemia
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Read more about Misdiagnosis and Tyrosinemia
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Visit our research pages for current research about Tyrosinemia treatments.
The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Tyrosinemia include:
Read more about Clinical Trials for Tyrosinemia
Types of Tyrosinemia
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Autosomal recessive defect in tyrosine metabolism resulting in liver and kidney disturbances and mental retardation - (Source - WordNet 2.1)
Tyrosinemia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Tyrosinemia, or a subtype of Tyrosinemia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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