cys·tin·uria noun \ˌsis-tə-ˈnu̇r-ē-ə, -ˈnyu̇r-\
: a metabolic defect characterized by excretion of excessive amounts of cystine in the urine and inherited as an autosomal recessive trait
Origin of CYSTINURIA
First Known Use: 1853
cys·tin·uria noun \ˌsis-tə-ˈn(y)u̇r-ē-ə\ (Medical Dictionary)
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