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syndrome matrix

См. также в других словарях:

  • Matrix gla protein — Identifiers Symbols MGP; MGLAP; NTI External IDs OMIM:  …   Wikipedia

  • Syndrome de Marfan — Référence MIM 154700 Transmission Dominante Chromosome 15q21 Gène FBN1 Mutation Ponctuelle …   Wikipédia en Français

  • Syndrome de marfan — Autre nom {{{Autre nom}}} Référence MIM 1 …   Wikipédia en Français

  • Marfan syndrome — Marfan redirects here. For the person after whom the syndrome is named, see Antoine Marfan. Marfan syndrome Classification and external resources Micrograph demonstrating myxomatous degeneration of the aorti …   Wikipedia

  • Hunter syndrome — Classification and external resources ICD 10 E76.1 ICD 9 277.5 …   Wikipedia

  • Kindler syndrome — Classification and external resources OMIM 173650 DiseasesDB 32778 eMedicine …   Wikipedia

  • Infant respiratory distress syndrome — Classification and external resources ICD 10 P22 ICD 9 769 …   Wikipedia

  • Keutel syndrome — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 33698 ICD10 = ICD9 = ICDO = OMIM = 245150 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Keutel syndrome is a rare autosomal recessive genetic disorder characterized by abnormal… …   Wikipedia

  • Winchester syndrome — in a rare congenital connective tissue disease described in 1969,cite journal |author=Winchester P, Grossman H, Lim WN, Danes BS |title=A new acid mucopolysaccharidosis with skeletal deformities simulating rheumatoid arthritis |journal=Am J… …   Wikipedia

  • 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

  • Turner syndrome — or Ullrich Turner syndrome encompasses several conditions, of which monosomy X is the most common. It is a chromosomal disorder affecting females in which all or part of one of the X chromosomes is absent. Occurring in 1 out of every 2500 girls,… …   Wikipedia

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