phenotypic deficiency

phenotypic deficiency
фенотипический дефицит

English-Russian small dictionary of medicine. . 2015.

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  • Carnitine palmitoyltransferase II deficiency — Classification and external resources Carnitine ICD 9 …   Wikipedia

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  • multiple sulfatase deficiency — an autosomal recessive lysosomal storage disease caused by a mutation in the SUMF1 gene (locus: 3p26), which encodes a factor necessary for catalytic activity of eukaryotic sulfatases, resulting in deficiency of at least nine lysosomal and… …   Medical dictionary

  • Androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 E …   Wikipedia

  • Partial androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 …   Wikipedia

  • syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …   Medical dictionary

  • Mild androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 E …   Wikipedia

  • Copper in health — Normal absorption and distribution of copper. Cu = copper, CP = ceruloplasmin, green = ATP7B carrying copper. Copper is an essential trace element that is vital to the health of all living things (humans, plants, animals, and microorganisms). In… …   Wikipedia

  • Tricho-hepato-enteric syndrome — Infobox Disease Name = PAGENAME Caption = Typical facial abnormalities with prominent forehead and cheeks, broad nasal root and wide spaced eyes. Abnormal hairs are woolly, easily removed and poorly pigmented. DiseasesDB = ICD10 = ICD9 = ICDO =… …   Wikipedia

  • Adaptation — This article is about the evolutionary process. For other uses, see Adaptation (disambiguation). Part of a series on Evolutionary Biology …   Wikipedia

  • Phenylketonuria — PKU redirects here. For other uses, see PKU (disambiguation). Phenylketonuria Classification and external resources ICD 10 E70.0 ICD 9 …   Wikipedia


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