Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Término preferido
Protein C Deficiency
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Tipo
-
mesh:Descriptor
Definición
- An absence or deficiency in PROTEIN C which leads to impaired regulation of blood coagulation. It is associated with an increased risk of severe or premature thrombosis. (Stedman's Med. Dict., 26th ed.)
Concepto genérico
Etiquetas alternativas
- Deficiency, Protein C
- Hereditary Thrombophilia Due To Protein C Deficiency
En otras lenguas
-
francés
URI
http://data.loterre.fr/ark:/67375/JVR-BT3JW1WS-T
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