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Factor VII Deficiency
An autosomal recessive characteristic or a coagulation disorder acquired in association with VITAMIN K DEFICIENCY. FACTOR VII is a Vitamin K dependent glycoprotein essential to the extrinsic pathway of coagulation.
推出的年份: 1985
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:
C15.378.100.100.310, C15.378.100.141.310, C15.378.463.310, C16.320.099.310
MeSH 单一 ID:
D005168
进入的组:
Deficiency, Factor Seven
Deficiencies, Factor Seven
Factor Seven Deficiencies
Factor Seven Deficiency
Hypoproconvertinemia
Hypoproconvertinemias
Deficiency, Factor VII
Deficiencies, Factor VII
Factor VII Deficiencies
Deficiency, Factor 7
Deficiencies, Factor 7
Factor 7 Deficiencies
Factor 7 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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