homocystinemia ho·mo·cys·ti·ne·mi·a (hō’mə-sĭs’tə-nē’mē-ə)
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

    homocytotropic antibody n. An antibody that has an affinity for mast cells of the same or of a closely related species and that, upon combining with a specific antigen, triggers the release of pharmacological mediators of anaphylaxis from the cells to which it attaches. Also called reaginic antibody.

  • Homodont

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

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