- Protein S deficiency disease
- S蛋白缺乏病
Medical Chinese dictionary (湘雅医学词典). 2013.
Protein S deficiency disease
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Protein C deficiency — Protein C is a protein in plasma that enters into the cascade of biochemical events leading to the formation of a clot. Deficiency of protein C results in thrombotic (clotting) disease and excess platelets with recurrent thrombophlebitis… … Medical dictionary
deficiency disease — n a disease (as scurvy) caused by a lack of essential dietary elements and esp. a vitamin or mineral * * * any disease caused by the lack of an essential nutrient in the diet. Such nutrients include vitamin, essential amino acid, and essential… … Medical dictionary
Protein C deficiency — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 10807 ICD10 = ICD9 = ICD9|289.81 ICDO = OMIM = 176860 MedlinePlus = eMedicineSubj = med eMedicineTopic = 1923 MeshID = D020151 Protein C deficiency is a rare genetic trait that predisposes to … Wikipedia
Protein S deficiency — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 10814 ICD10 = ICD9 = ICD9|289.81 ICDO = OMIM = 176880 MedlinePlus = eMedicineSubj = med eMedicineTopic = 1924 MeshID = D018455 Protein S deficiency is a disorder associated with increased… … Wikipedia
Thrombotic disease due to protein C deficiency — Protein C is a protein in plasma that enters into the cascade of biochemical events leading to the formation of a clot. Deficiency of protein C results in thrombotic (clotting) disease and excess platelets with recurrent thrombophlebitis… … Medical dictionary
Protein S — is a vitamin K dependent plasma glycoprotein synthesized in the liver. In the circulation, Protein S exists in two forms: a free form and a complex form bound to complement protein C4b. FunctionThe best characterized function of Protein S is its… … Wikipedia
Protein C — Not to be confused with C peptide, C reactive protein, or protein kinase C. Protein C (inactivator of coagulation factors Va and VIIIa) Tertiary structure of human activated protein C (minus the Gla domain … Wikipedia
Disease, Tay-Sachs (TSD) — Deficiency of hexosaminidase A causes a disorder known as Tay Sachs disease (TSD) which is concisely defined by OMIM (Online Mendelian Inheritance in Man) as “an autosomal recessive, progressive neurodegenerative disorder, which in the classic… … Medical dictionary
Deficiency of the interleukin-1–receptor antagonist — Classification and external resources OMIM 612852 Deficiency of the interleukin 1–receptor antagonist (DIRA) is a rare, autosomal recessive, genetic autoinflammatory syndrome resulting from mutations in IL1RN, the gene encoding the … Wikipedia
Protein Z-related protease inhibitor — protein Name = caption = width = HGNCid = 15996 Symbol = SERPINA10 AltSymbols = EntrezGene = 51156 OMIM = 605271 RefSeq = NM 016186 UniProt = Q9UK55 PDB = ECnumber = Chromosome = 14 Arm = q Band = 32.1 LocusSupplementaryData = Protein Z dependent … Wikipedia
Protein (nutrient) — This article is about protein as a nutrient. For protein as a class of molecule, see protein. For other uses, see bodybuilding supplement. Amino acids are the building blocks of protein. Proteins are polymer chains made of amino acids linked… … Wikipedia
