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
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
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
Protein Z — protein Name = protein Z caption = width = HGNCid = 9460 Symbol = PROZ AltSymbols = EntrezGene = 8858 OMIM = 176895 RefSeq = NM 003891 UniProt = P22891 PDB = ECnumber = Chromosome = 13 Arm = q Band = 34 LocusSupplementaryData = Protein Z is a… … Wikipedia
Protein combining — (also protein complementing) is a controversial theory that vegetarians, particlarly vegans, must eat certain complementary foods like beans and rice together in the same meal. The purpose of protein combining is to ensure that plant foods with… … 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
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
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
