Medical dictionary. 2011.
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
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
Compound heterozygosity — in medical genetics is the condition of having two heterogeneous recessive alleles at a particular locus that can cause genetic disease in a heterozygous state. Compound heterozygosity reflects the diversity of the mutation base for many… … Wikipedia
Genetics — This article is about the general scientific term. For the scientific journal, see Genetics (journal). Part of a series on Genetics Key components Chromosome DNA • RNA Genome … Wikipedia
Public Health Genomics — is the utilization of genomics information to benefit public health. This is visualized as more effective personalised preventive care and disease treatments with better specificity, targeted to the genetic makeup of each patient. (Bellagio Group … Wikipedia
Aspartame — Aspartame[1] … Wikipedia
Phenylalanine — Phe redirects here. For other uses, see Phe (disambiguation). Phenylalanine … Wikipedia
List of diseases (P) — A list of diseases in the English Wikipedia.DiseasesTOC PaPac Pal* Pachydermoperiostosis * Pachygyria * Pachyonychia congenita Jackson Lawler type * Pacman dysplasia * Paes Whelan Modi syndrome * Paget disease extramammary * Paget disease… … Wikipedia
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
Newborn screening — See also: Apgar score Newborn screening Intervention MeSH D015997 Newborn screening is the process by which infants are screened shortly after birth for a list of disorders that are treatable, but di … Wikipedia
