Homocystinemia


homocystinemia ho·mo·cys·ti·ne·mi·a (hō’mə-sĭs’tə-nē’mē-ə)
n.
The presence of an excess of homocystine in plasma.

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  • Homocystinuria

    homocystinuria ho·mo·cys·ti·nu·ri·a (hō’mə-sĭs’tə-nur’ē-ə, -nyur’-) n. An inherited metabolic disorder caused by a deficiency of an enzyme important in the metabolism of homocystine and characterized by the excretion of homocystine in the urine, mental retardation, dislocation of the crystalline lens of the eye, sparse blond hair, and cardiovascular and skeletal deformities.

  • Homocytotropic

    homocytotropic ho·mo·cy·to·trop·ic (hō’mō-sī’tə-trŏp’ĭk, -trō’pĭk) adj. Relating to or having an affinity for cells of the species in which it originated, as of an antibody.

  • Homocytotropic antibody

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  • Homodont

    /ˈhəʊməˌdɒnt/ adjective 1. (of most nonmammalian vertebrates) having teeth that are all of the same type Compare heterodont

  • Homodyne

    [hoh-muh-dahyn, hom-uh-] /ˈhoʊ məˌdaɪn, ˈhɒm ə-/ adjective, Radio. 1. of or relating to reception by a device that generates a varying voltage of the same or nearly the same frequency as the incoming carrier wave and combines it with the incoming signal for detection.


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