Phenylketonuria — PKU redirects here. For other uses, see PKU (disambiguation). Phenylketonuria Classification and external resources ICD 10 E70.0 ICD 9 … Wikipedia
MPKUCS — Maternal Phenylketonuria Collaborative Study … Medical dictionary
MPKUCS — • Maternal Phenylketonuria Collaborative Study … Dictionary of medical acronyms & abbreviations
Neurodevelopmental disorder — A boy with microcephaly and his schoolmates. Microcephaly is a neurodevelopmental disorder. A neurodevelopmental disorder,[1] or disorder of neural devel … Wikipedia
Phénylcétonurie — Classification et ressources externes CIM 10 E70.0 CIM 9 270.1 OMIM … Wikipédia en Français
hyperphenylalaninemia — The presence of abnormally high blood levels of phenylalanine, which may or may not be associated with elevated tyrosine levels, in newborn infants (premature and full term), associated with the heterozygous state of phenylketonuria, maternal… … Medical dictionary
ФЕНИЛКЕТОНУРИЯ — мед. Фенилкетонурия (ФКУ) врождённое заболевание, вызванное нарушением перехода фенилаланина в тирозин и приводящее к задержке психического развития. Частота. Выявлены значительные этнические и географические различия в частоте разных мутаций при … Справочник по болезням
heredity — /heuh red i tee/, n., pl. heredities. Biol. 1. the transmission of genetic characters from parents to offspring: it is dependent upon the segregation and recombination of genes during meiosis and fertilization and results in the genesis of a new… … Universalium
genetic disease, human — Introduction any of the diseases and disorders that are caused by mutations in one or more genes (gene). With the increasing ability to control infectious and nutritional diseases in developed countries, there has come the realization … Universalium
Medical genetics — Clinical genetics redirects here. For the journal, see Clinical Genetics (journal). For a non technical introduction to the topic, see Introduction to Genetics. Part of a series on Genetics Key components Chromosome … Wikipedia