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Up to: Inborn disorder of amino acid metabolism
Urea cycle disorder
A genetic inborn error of metabolism characterized by the deficiency of one of the enzymes necessary for the urea cycle. It results in accumulation of ammonia in the body.
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Urea cycle disorder or inherited hyperammonemia 0 trials · 24 incl. sub-types Sub-types →
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Citrullinemia 2 trials · 6 incl. sub-types Sub-types →