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alkaptonuria |
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alkaptonuria [al‚kap·tə′nür·ē·ə] (medicine) A hereditary metabolic disorder transmitted as an autosomal recessive in humans in which large amounts of homogentisic acid (alkapton) are excreted in the urine due to a deficiency of homogentisic acid oxidase. Also spelled alcaptonuria. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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