6501

\sˈɪks θˈa͡ʊzənd fˈa͡ɪvhˈʌndɹədən wˈɒn], \sˈɪks θˈa‍ʊzənd fˈa‍ɪvhˈʌndɹədən wˈɒn], \s_ˈɪ_k_s θ_ˈaʊ_z_ə_n_d f_ˈaɪ_v_h_ˈʌ_n_d_ɹ_ə_d_ə_n w_ˈɒ_n]\
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1985 - The Free On-line Dictionary of Computing
By Denis Howe

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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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