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Gray Platelet Syndrome
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.
推出的年份: 2009
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C15.378.140.427, C16.320.099.417
MeSH 单一 ID:
D055652
进入的组:
Gray Platelet Syndromes
Syndrome, Gray Platelet
Syndromes, Gray Platelet
Grey Platelet Syndrome
Grey Platelet Syndromes
Platelet Syndromes, Grey
Syndrome, Grey Platelet
Platelet alpha-Granule Deficiency
Platelet alpha Granule Deficiency
Platelet alpha-Granule Deficiencies
alpha-Granule Deficiencies, Platelet
alpha-Granule Deficiency, Platelet
早前的内容:
Blood Platelet Disorders (1971-2008)
All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Blood Platelet Disorders [C15.378.140]
Bernard-Soulier Syndrome [C15.378.140.120]
Gray Platelet Syndrome [C15.378.140.427]
Platelet Storage Pool Deficiency [C15.378.140.735]
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Thrombasthenia [C15.378.140.810]
Thrombocytopenia [C15.378.140.855]
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Thrombocytosis [C15.378.140.860]
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von Willebrand Diseases [C15.378.140.900]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Blood Coagulation Disorders, Inherited [C16.320.099]
Activated Protein C Resistance [C16.320.099.037]
Afibrinogenemia [C16.320.099.056]
Antithrombin III Deficiency [C16.320.099.075]
Bernard-Soulier Syndrome [C16.320.099.080]
Factor V Deficiency [C16.320.099.300]
Factor VII Deficiency [C16.320.099.310]
Factor X Deficiency [C16.320.099.320]
Factor XI Deficiency [C16.320.099.325]
Factor XII Deficiency [C16.320.099.330]
Factor XIII Deficiency [C16.320.099.335]
Gray Platelet Syndrome [C16.320.099.417]
Hemophilia A [C16.320.099.500]
Hemophilia B [C16.320.099.510]
Hermanski-Pudlak Syndrome [C16.320.099.515]
Hypoprothrombinemias [C16.320.099.550]
Protein C Deficiency [C16.320.099.690]
Thrombasthenia [C16.320.099.820]
von Willebrand Diseases [C16.320.099.920]
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Wiskott-Aldrich Syndrome [C16.320.099.970]
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