×
Close
註冊
登入
主页
用户
博客
照片
视频
医学图书S馆
医学图书M馆
医学图书D馆
医学术语
群组
活动
用户工具
用户指南
问答
谁看过我
反馈
语言
English
中文
推广
所有
MeSH descriptor
Mesh Subheading
Mesh Supplementary Concept
Mesh Pharmacological Action
search
搜索
清除所有
MeSH 搜索器
AND
OR
加入MeSH搜索引擎
搜索PubMed论文列
清除所有
Factor XIII Deficiency
A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical hemorrhagic diathesis.
推出的年份: 1973
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:
C15.378.100.100.335, C15.378.100.141.335, C15.378.463.335, C16.320.099.335
MeSH 单一 ID:
D005177
进入的组:
Deficiency, Factor Thirteen
Deficiencies, Factor Thirteen
Factor Thirteen Deficiencies
Factor Thirteen Deficiency
Deficiency, Factor XIII
Deficiencies, Factor XIII
Factor XIII Deficiencies
Deficiency, Factor 13
Deficiencies, Factor 13
Factor 13 Deficiencies
Factor 13 Deficiency
早前的内容:
Hemorrhagic Diathesis (1966-1972)
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]
thumb_up
Like
share
分享
favorite
书签
0
0
0
0
0
0
0
留言 (
0
)
gif
登入或註冊以發表你的留言
Modal title
×
Modal title
×
分享
登入
Global News and Health Forum
Join Now!
馬上登入
記住我
忘記密碼?
或者使用
Linkedin
留言 (0)