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Aminoaciduria, hyperdibasic, type 1

Orpha number ORPHA1032
Prevalence of rare diseases -
Inheritance -
Age of onset -
ICD 10 code -
MIM number
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Summary

Hyperdibasic aminoaciduria, type 1 is characterised by increased renal clearance of lysine, ornithine and arginine, in the presence of normal concentrations of cystine. Heterozygous individuals are asymptomatic but homozygotes display intellectual deficit. To date, 25 heterozygotes and one homozygote have been reported. *Author: Orphanet (September 2006)*.

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