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Hypoprothrombinemias
Absence or reduced levels of PROTHROMBIN in the blood.
推出的年份:
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
congenital
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:
C15.378.100.100.550, C15.378.100.141.550, C15.378.463.550, C16.320.099.550
MeSH 单一 ID:
D007020
进入的组:
Prothrombin Deficiency
Deficiencies, Prothrombin
Deficiency, Prothrombin
Prothrombin Deficiencies
Hypoprothrombinemia
Deficiency, Factor II
Deficiencies, Factor II
Factor II Deficiencies
Factor II Deficiency
All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Blood Coagulation Disorders [C15.378.100]
Blood Coagulation Disorders, Inherited [C15.378.100.100]
Activated Protein C Resistance [C15.378.100.100.037]
Afibrinogenemia [C15.378.100.100.056]
Antithrombin III Deficiency [C15.378.100.100.075]
Bernard-Soulier Syndrome [C15.378.100.100.080]
Factor V Deficiency [C15.378.100.100.300]
Factor VII Deficiency [C15.378.100.100.310]
Factor X Deficiency [C15.378.100.100.320]
Factor XI Deficiency [C15.378.100.100.325]
Factor XII Deficiency [C15.378.100.100.330]
Factor XIII Deficiency [C15.378.100.100.335]
Hemophilia A [C15.378.100.100.500]
Hemophilia B [C15.378.100.100.510]
Hermanski-Pudlak Syndrome [C15.378.100.100.515]
Hypoprothrombinemias [C15.378.100.100.550]
Protein C Deficiency [C15.378.100.100.690]
Thrombasthenia [C15.378.100.100.820]
von Willebrand Diseases [C15.378.100.100.900]
add_circle
Wiskott-Aldrich Syndrome [C15.378.100.100.970]
All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Blood Coagulation Disorders [C15.378.100]
Coagulation Protein Disorders [C15.378.100.141]
Activated Protein C Resistance [C15.378.100.141.036]
Afibrinogenemia [C15.378.100.141.072]
Factor V Deficiency [C15.378.100.141.300]
Factor VII Deficiency [C15.378.100.141.310]
Factor X Deficiency [C15.378.100.141.320]
Factor XI Deficiency [C15.378.100.141.325]
Factor XII Deficiency [C15.378.100.141.330]
Factor XIII Deficiency [C15.378.100.141.335]
Hemophilia A [C15.378.100.141.500]
Hemophilia B [C15.378.100.141.510]
Hypoprothrombinemias [C15.378.100.141.550]
von Willebrand Diseases [C15.378.100.141.900]
add_circle
All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Hemorrhagic Disorders [C15.378.463]
Afibrinogenemia [C15.378.463.067]
Bernard-Soulier Syndrome [C15.378.463.080]
Disseminated Intravascular Coagulation [C15.378.463.250]
Factor V Deficiency [C15.378.463.300]
Factor VII Deficiency [C15.378.463.310]
Factor X Deficiency [C15.378.463.320]
Factor XI Deficiency [C15.378.463.325]
Factor XII Deficiency [C15.378.463.330]
Factor XIII Deficiency [C15.378.463.335]
Hemophilia A [C15.378.463.500]
Hemophilia B [C15.378.463.510]
Hemostatic Disorders [C15.378.463.515]
add_circle
Hypoprothrombinemias [C15.378.463.550]
Platelet Storage Pool Deficiency [C15.378.463.735]
add_circle
Purpura, Thrombocytopenic, Idiopathic [C15.378.463.740]
Thrombasthenia [C15.378.463.810]
Thrombocythemia, Essential [C15.378.463.825]
Vitamin K Deficiency [C15.378.463.841]
add_circle
von Willebrand Diseases [C15.378.463.920]
add_circle
Waterhouse-Friderichsen Syndrome [C15.378.463.950]
Wiskott-Aldrich Syndrome [C15.378.463.960]
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]
add_circle
Wiskott-Aldrich Syndrome [C16.320.099.970]
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