Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Término preferido
Gray Platelet Syndrome
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Tipo
-
mesh:Descriptor
Definición
- A rare, inherited platelet disorder characterized by a selective deficiency in the number and contents of platelet alpha-granules. It is associated with THROMBOCYTOPENIA, enlarged platelets, and prolonged bleeding time.
Concepto genérico
Etiquetas alternativas
- Grey Platelet Syndrome
En otras lenguas
-
francés
-
Maladie du pool vide alpha
-
SPG (Syndrome des Plaquettes Grises)
URI
http://data.loterre.fr/ark:/67375/JVR-HLGX3VHP-M
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