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Hyperdibasic aminoaciduria type 2: A rare inborn urea cycle disorder characterized by an enzyme defect in the amino acid transporter gene SLC7A7 (positive amino acid transporter). More detailed information about the symptoms, causes, and treatments of Hyperdibasic aminoaciduria type 2 is available below.
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Prognosis for Hyperdibasic aminoaciduria type 2: The prognosis is variable depending on how well the condition is managed and whether lung complications develop.
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