CL71,563

\sˌiːˈɛl sˈɛvəntiwˈɒn θˈa͡ʊzənd fˈa͡ɪvhˈʌndɹədən sˈɪkstiθɹˈiː], \sˌiːˈɛl sˈɛvəntiwˈɒn θˈa‍ʊzənd fˈa‍ɪvhˈʌndɹədən sˈɪkstiθɹˈiː], \s_ˌiː__ˈɛ_l s_ˈɛ_v_ə_n_t_i_w_ˈɒ_n θ_ˈaʊ_z_ə_n_d_ f_ˈaɪ_v_h_ˈʌ_n_d_ɹ_ə_d_ə_n s_ˈɪ_k_s_t_i_θ_ɹ_ˈiː]\

Definitions of CL71,563

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MEN IIa

  • type multiple endocrine neoplasia characterized by virtually 100% incidence medullary thyroid carcinoma, a 50% pheochromocytoma, and lesser adenomas associated hyperparathyroidism. condition always transmitted through autosomal dominant inheritance. Genetic testing can identify individuals with the trait in early infancy. Treatment is usually excision of enlarged parathyroid glands. (From Holland et al., Cancer Medicine, 3d ed, pp1172-75)
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