| 疾病名称 |
别名 |
|
| Factor Xi Deficiency |
|
Plasma Thromboplastin Antecedent Deficiency
|
Rosenthal Syndrome
|
|
Pta Deficiency
|
Hemophilia C
|
|
Rosenthal Factor Deficiency
|
F11 Deficiency
|
|
Congenital Factor Xi Deficiency
|
Hereditary Factor Xi Deficiency Disease
|
|
Haemophilia C
|
Factor Xi Deficiency, Autosomal Dominant
|
|
Rosenthal'S Disease
|
Factor 11 Deficiency
|
|
Factor Xi
|
Factor Xi Deficiency, Autosomal Recessive
|
|
Factor Xi Deficiency, Congenital
|
FA11D
|
|
Thromboplastin Antecedent Deficiency
|
Pta - [Plasma Thromboplastin Antecedent] Deficiency
|
|
Congenital Factor Xi Deficiency Disease
|
Rosenthal Disease
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| Hemorrhagic Disease |
|
Hemorrhagic Disorders
|
Hemorrhagic Diathesis
|
|
Hemorrhagic Diseases
|
Bleeding Tendency
|
|
Acquired Coagulation Factor Inhibitor Disorder
|
Acquired Inhibitor Of Coagulation
|
|
Antithrombinaemia
|
Antithromboplastinogenaemia
|
|
Circulating Anticoagulant Disorder
|
Haemorrhagic Disorder Due To Antithrombinaemia
|
|
Haemorrhagic Disorder Due To Excess Administered Heparin
|
Antithromboplastinaemia
|
|
Haemorrhagic Disorder Due To Hyperheparinemia
|
|
|
| Factor X Deficiency |
|
Stuart-Prower Factor Deficiency
|
F10 Deficiency
|
|
Congenital Stuart Factor Deficiency
|
Factor X Deficiency, Congenital
|
|
Congenital Factor X Deficiency
|
Disease, Stuart-Prower
|
|
Stuart Factor Deficiency, Congenital
|
FA10D
|
|
Factor 10 Deficiency
|
Deficiency, Factor X
|
|
Hereditary Factor X Deficiency Disease
|
Deficiency Of Factor X
|
|
Stuart Deficiency Disease
|
Stuart Prower Deficiency
|
|
Stuart-Prower Disease
|
|
|
| Von Willebrand'S Disease |
|
Von Willebrand Disease
|
Von Willebrand Disorder
|
|
Vascular Pseudohemophilia
|
Hereditary Von Willebrand Disease
|
|
Vwd
|
Vascular Hemophilia
|
|
Von Willebrand'S-Jurgens' Disease
|
Von Willebrand-Jrgens Disease
|
|
Von Willebrand Factor Deficiency
|
Von Willebrand Factor, Deficiency
|
|
Angiohemophilia
|
Von Willebrand'S Factor Deficiency
|
|
Von Willebrand Diseases
|
Factor Viii Deficiency With Vascular Defect
|
|
Vascular Haemophilia
|
Willebrand Jurgen Thrombopathy
|
|
Pseudohaemophilia
|
Minot-Von Willebrand-Jurgen Disease
|
|
Angiohaemophilia
|
Angiohaemophilia A
|
|
Angiohaemophilia B
|
|
|
| Hemophilia B |
|
Christmas Disease
|
Factor Ix Deficiency
|
|
F9 Deficiency
|
HEMB
|
|
Plasma Thromboplastin Component Deficiency
|
Congenital Factor Ix Deficiency
|
|
Mild Hemophilia B
|
Severe Hemophilia B
|
|
Congenital Factor Ix Disorder
|
Deficiency, Functional Factor Ix
|
|
Hem B
|
Mild Congenital F9 Deficiency
|
|
Mild Congenital Factor Ix Deficiency
|
Moderate Hemophilia B
|
|
Moderate Congenital F9 Deficiency
|
Moderate Congenital Factor Ix Deficiency
|
|
Severe Congenital F9 Deficiency
|
Severe Congenital Factor Ix Deficiency
|
|
Bleeding Disorder In Hemophilia B Carriers
|
Congenital F9 Deficiency
|
|
Recessive X-Linked Hemophilia B
|
|
|
| Thrombophilia |
|
|
| Afibrinogenemia, Congenital |
|
Congenital Afibrinogenemia
|
Afibrinogenemia
|
|
Factor I Deficiency
|
Familial Afibrinogenemia
|
|
Hypofibrinogenemia, Congenital
|
Fibrinogen Deficiency
|
|
Afibrinogenemia Congenital
|
CAFBN
|
|
Congenital Hypofibrinogenemia
|
Hypofibrinogenemia
|
|
Complement Factor I Deficiency
|
|
|
| Thrombosis |
|
Thrombosis Of Blood Vessel
|
|
|
| High Molecular Weight Kininogen Deficiency |
|
HMWK DEFICIENCY
|
Fitzgerald Trait
|
|
Congenital High-Molecular-Weight Kininogen Deficiency
|
Flaujeac Factor Deficiency
|
|
Kininogen Deficiency, High Molecular Weight
|
Kininogen Deficiency
|
|
Hmwk
|
High-Molecular-Weight Kininogen Deficiency, Congenital
|
|
|
| Pyruvate Kinase Deficiency Of Red Cells |
|
Pyruvate Kinase Deficiency
|
Pk Deficiency
|
|
Pyruvate Kinase Deficiency Of Erythrocyte
|
Hemolytic Anemia Due To Red Cell Pyruvate Kinase Deficiency
|
|
Pyruvate Kinase Deficiency Of Erythrocytes
|
Pkd
|
|
PKRD
|
Hereditary Non-Spherocytic Hemolytic Anemia Due To Pyruvate Kinase Deficiency
|
|
Hnsha
|
Pyruvate Kinase-Deficient Hemolytic Anemia
|
|
Red Cell Pyruvate Kinase Deficiency
|
Deficiency Of Pyruvate Kinase
|
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
|
|
| Disseminated Intravascular Coagulation |
|
Defibrination Syndrome
|
Dic
|
|
Diffuse Or Disseminated Intravascular Coagulation
|
Fibrinolytic Purpura
|
|
Consumption Coagulopathy
|
Diffuse Intravascular Coagulation
|
|
Dic - [Disseminated Intravascular Coagulation]
|
Disseminated Intravascular Coagulopathy
|
|
Fibrinolysis Nos
|
Thrombolytic Purpura
|
|
|
| Puerperal Pulmonary Embolism |
|
Obstetric Pulmonary Embolism
|
|
|
| Carotid Artery Occlusion |
|
Occlusion And Stenosis Of Carotid Artery
|
|
|
| Congenital Nonspherocytic Hemolytic Anemia |
|
Hereditary Non-Spherocytic Hemolytic Anemia
|
Hereditary Nonspherocytic Hemolytic Anemia
|
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
Congenital Nonspherocytic Hemolytic Anaemia
|
|
Hereditary Nonspherocytic Hemolytic Anaemia
|
Hnsha
|
|
|
| Occlusion Precerebral Artery |
|
Occlusion And Stenosis Of Multiple And Bilateral Precerebral Arteries
|
Occlusion And Stenosis Of Precerebral Artery
|
|
|
| Prothrombin Deficiency |
|
Factor Ii Deficiency
|
Hypoprothrombinemia
|
|
Dysprothrombinemia
|
Deficiency, Prothrombin
|
|
Inherited Factor Ii Deficiency
|
Hereditary Factor Ii Deficiency Disease
|
|
|
| Factor Xii Deficiency |
|
Hageman Factor Deficiency
|
Haf Deficiency
|
|
Factor Xii Deficiency Disease
|
F12 Deficiency
|
|
Deficiency, Hageman
|
Coagulation Factor 12 Deficiency
|
|
Factor 12 Deficiency
|
Congenital Factor Xii Deficiency
|
|
Congenital Hageman Factor Deficiency
|
FA12D
|
|
Factor Xii
|
Deficiency, Factor Xii
|
|
|
| Hemarthrosis |
|
Haemarthrosis Of Shoulder Joint
|
Haemarthrosis Of The Ankle And Foot
|
|
Haemarthrosis Of The Pelvic Region And Thigh
|
Hemarthrosis Involving Ankle And Foot
|
|
Hemarthrosis Involving Forearm
|
Hemarthrosis Involving Hand
|
|
Hemarthrosis Involving Lower Leg
|
Hemarthrosis Involving Pelvic Region And Thigh
|
|
Hemarthrosis Involving Shoulder Region
|
Hemarthrosis Involving Upper Arm
|
|
Hemarthrosis Of Ankle And/Or Foot
|
Hemarthrosis Of Forearm
|
|
Hemarthrosis Of Hand
|
Hemarthrosis Of Lower Leg
|
|
Hemarthrosis Of Shoulder
|
Hemarthrosis Of Shoulder Region
|
|
Hemarthrosis Of The Ankle And Foot
|
Hemarthrosis Of The Ankle And/Or Foot
|
|
Hemarthrosis Of The Forearm
|
Hemarthrosis Of The Hand
|
|
Hemarthrosis Of The Lower Leg
|
Hemarthrosis Of The Pelvic Region And Thigh
|
|
Hemarthrosis Of The Shoulder Region
|
Hemarthrosis Of The Upper Arm
|
|
Hemarthrosis Of Upper Arm
|
|
|
| Hereditary Combined Deficiency Of Vitamin K-Dependent Clotting Factors |
|
Hereditary Combined Deficiency Of Factors Ii, Vii, Ix And X
|
Vkcfd
|
|
|
| Factor Viii Deficiency |
|
Autosomal Hemophilia A
|
Hemophilia A
|
|
Autosomal Factor Viii Deficiency
|
Classic Hemophilia A
|
|
Congenital Factor Viii Disorder
|
Subhemophilia
|
|
Factor 8 Deficiency, Congenital
|
Factor Viii
|
|
|
| Post-Thrombotic Syndrome |
|
Postphlebitic Syndrome
|
Postthrombotic Syndrome
|
|
Postphlebetic Syndrome With Inflammation
|
Postphlebetic Syndrome With Ulcer
|
|
Postphlebetic Syndrome With Ulcer And Inflammation
|
Venous Stress Disorder
|
|
|
| Acquired Von Willebrand Syndrome |
|
Acquired Von Willebrand Disease
|
Willebrand Disease, Acquired
|
|
Avws
|
|
|
| Carotid Artery Thrombosis |
|
|
| Factor Xiii Deficiency |
|
Hereditary Factor Xiii Deficiency Disease
|
Deficiency, Laki-Lorand Factor
|
|
Congenital Factor Xiii Deficiency
|
Fibrin Stabilizing Factor Deficiency
|
|
Deficiency, Factor Xiii
|
Factor Xiii Deficiency Disease
|
|
Deficiency Of Factor Xiii
|
Fibrin-Stabilizing Factor Deficiency
|
|
Factor Xiii Deficiency, Congenital
|
|
|
| Hereditary Angioedema |
|
Hereditary Angioneurotic Edema
|
Hereditary Angioedema Type 1
|
|
Hane
|
Angioedema, Hereditary
|
|
Hae
|
Angioedemas, Hereditary
|
|
Deficiency Of C1 Esterase Inhibitor
|
C1 Esterase Inhibitor Deficiency
|
|
C1 Inhibitor Deficiency
|
Familial Angioneurotic Edema
|
|
Hereditary Bradykinine-Induced Angioedema
|
Hereditary Non Histamine-Induced Angioedema
|
|
Hae 1
|
Hae-I
|
|
Hereditary Angioneurotic Edema Type 1
|
Hereditary C1 Esterase Inhibitor Deficiency - Deficient Factor
|
|
Hereditary Angioedema Types I And Ii
|
Hereditary Angioneurotic Oedema
|
|
Familial Angioedema
|
Hae - [Hereditary Angioneurotic Oedema]
|
|
Bannister Disease, Hereditary
|
Quincke Disease Or Oedema
|
|
Hereditary Quincke Oedema
|
|
|
| Blood Coagulation Disease |
|
Blood Coagulation Disorders
|
Coagulation Protein Disease
|
|
Inherited Blood Coagulation Disease
|
Postpartum Coagulation Defect
|
|
Postpartum Coagulation Defect With Delivery
|
Coagulation Protein Disorders
|
|
Puerperal Coagulopathy
|
|
|
| Intracranial Thrombosis |
|
Cerebral Thrombosis
|
Thrombosis Of Cerebral Veins
|
|
Cerebral Arterial Thrombosis
|
|
|
| Myocardial Infarction |
|
Heart Attack
|
Myocardial Infarction, Susceptibility To
|
|
Myocardial Infarction 1
|
Myocardial Infarction, Protection Against
|
|
Myocardial Infarction, Decreased Susceptibility To
|
Myocardial Infarction, Decreased
|
|
Myocardial Infarct
|
MCI1
|
|
Premature Myocardial Infarction
|
Myocardial Infarction, Susceptibility To, Type 1
|
|
|
| Pulmonary Artery Disease |
|
Abnormality Of The Pulmonary Artery
|
|
|
| Hypotrichosis 13 |
|
HYPT13
|
Hypotrichosis With Woolly Hair
|
|
Hypotrichosis, Type 13
|
|
|
| Bernard-Soulier Syndrome |
|
Giant Platelet Syndrome
|
BSS
|
|
Von Willebrand Factor Receptor Deficiency
|
Bdplt1
|
|
Platelet Glycoprotein Ib Deficiency
|
Bernard-Soulier Syndrome, Type A1
|
|
Bernard-Soulier Syndrome, Type B
|
Bernard Soulier Syndrome
|
|
Deficiency Of Platelet Glycoprotein 1b
|
Hemorrhagiparous Thrombocytic Dystrophy
|
|
Bernard-Soulier Syndrome Type C
|
Bleeding Disorder, Platelet-Type, 1
|
|
Glycoprotein Ib, Platelet, Deficiency Of
|
Giant Platelet Disorder, Isolated
|
|
Giant Platelet Disease
|
Macrothrombocytopenia, Familial Bernard-Soulier Type
|
|
Bernard-Soulier Syndrome, Type C
|
Bernard - Soulier Thrombopathy
|
|
Hemorrhagic Dystrophic Thrombocytopenia
|
Thrombopathy, Bernard-Soulier
|
|
Platelet Glycoprotein 1b, Deficiency Of
|
Hemorrhagioparous Thrombocytic Dystrophy
|
|
Bernard-Soulier Syndrome Type A1
|
Bernard-Soulier Syndrome Type B
|
|
Bleeding Disorder Platelet-Type 1
|
Gpd
|
|
Macrothrombocytopenia, Familial, Bernard-Soulier Type
|
|
|
