The way property values are displayed:
The way concept relations are shown:
The way concept relations are shown:
Protein S Deficiency
Hierarchy: | ∟ ∟ ∟ ∟ Protein S Deficiency 17 coordinate concepts∟ ∟ ∟ ∟ Protein S Deficiency 17 coordinate concepts∟ ∟ ∟ ∟ Protein S Deficiency 17 coordinate conceptsX |
Broader terms: | |
Annotation: | a blood protein disord causing thromboses; DF: PROTEIN S DEFIC
X |
History note: | |
historyNote*: | 95
X |
publicMeSHNote*: | 95
X |
Scope note: | An autosomal dominant disorder showing decreased levels of plasma protein S antigen or activity, associated with venous thrombosis and pulmonary embolism. PROTEIN S is a vitamin K-dependent plasma protein that inhibits blood clotting by serving as a cofactor for activated PROTEIN C (also a vitamin K-dependent protein), and the clinical manifestations of its deficiency are virtually identical to those of protein C deficiency. Treatment with heparin for acute thrombotic processes is usually followed by maintenance administration of coumarin drugs for the prevention of recurrent thrombosis. (From Harrison's Principles of Internal Medicine, 12th ed, p1511; Wintrobe's Clinical Hematology, 9th ed, p1523)
X |
activeMeSHYear*: | |
dateCreated*: | 1994-04-16X |
dateEstablished*: | 1995-01-01X |
dateRevised*: | 1998-06-10X |
recordAuthorizer*: | SJNX |
recordMaintainer*: | NNSX |
recordOriginator*: | TGCX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Proteiini S:n puutos (fi) XProteiinin S puutos (fi, replaced) Proteiinin S puute (fi, replaced) Proteiini S:n puute (fi, replaced) Protein S-brist (sv) Deficiency, Protein S (en, replaced) |
Share: |
Loading results...