| Diseases |
Alias |
|
| 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
|
|
|
| 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
|
|
|
| Scott Syndrome |
|
SCTS
|
Bdplt7
|
|
Prothrombin Consumption Deficiency
|
Bleeding Abnormality Due To Deficiency Of Platelet Binding Of Factor X
|
|
Bleeding Disorder, Platelet-Type, 7
|
Prothrombin Conversion Defect, Familial
|
|
Prothrombin Consumption Inhibitor, Familial
|
Bleeding Abnormality Due To Deficiency Of Platelet Biding Of Factor X
|
|
Familial Prothrombin Consumption Inhibitor
|
Familial Prothrombin Conversion Defect
|
|
Platelet-Type Bleeding Disorder 7
|
Platelet Factor X Receptor Deficiency
|
|
Bleeding Disorder Platelet-Type 7
|
Prothrombin Consumption Inhibitor Familial
|
|
Prothrombin Conversion Defect Familial
|
|
|
| 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
|
|
|
| Hemophilia A |
|
Factor Viii Deficiency
|
Haemophilia A
|
|
Mild Hemophilia A
|
HEMA
|
|
Hemophilia, Classic
|
Classic Hemophilia
|
|
Factor 8 Deficiency
|
Severe Hemophilia A
|
|
Classical Hemophilia
|
Hem A
|
|
Hemophilia A, Congenital
|
Mild Congenital F8 Deficiency
|
|
Mild Congenital Factor Viii Deficiency
|
Severe Congenital F8 Deficiency
|
|
Severe Congenital Factor Viii Deficiency
|
Moderate Hemophilia A
|
|
Moderate Congenital F8 Deficiency
|
Moderate Congenital Factor Viii Deficiency
|
|
Bleeding Disorder In Hemophilia A Carriers
|
Congenital F8 Deficiency
|
|
Congenital Fviii Deficiency
|
Congenital Factor Viii Deficiency
|
|
Mild Hereditary Factor Viii Deficiency Disease
|
Severe Hereditary Factor Viii Deficiency Disease
|
|
Ahg - [Antihaemophilic Globulin] Deficiency
|
Ahg - [Antihaemophilic Globulin] Deficiency Disease
|
|
Congenital Factor Viii Disorder
|
Sex-Linked Factor Viii Deficiency
|
|
Antihaemophilic Globulin Deficiency
|
Classic Haemophilia
|
|
Familial Haemophilia
|
Haemophilia
|
|
Hereditary Haemophilia
|
Subhaemophilia
|
|
Haemophilia Nos
|
|
|
| Carotid Artery Thrombosis |
|
|
| 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
|
|
|
| Antithrombin Iii Deficiency |
|
Hereditary Antithrombin Deficiency
|
Congenital Antithrombin Iii Deficiency
|
|
Hereditary Thrombophilia Due To Congenital Antithrombin Deficiency
|
AT3D
|
|
Thrombophilia Due To Antithrombin Iii Deficiency
|
Thph7
|
|
Hereditary Thrombophilia Due To Congenital Antithrombin 3 Deficiency
|
Thrombophilia 7 Due To Antithrombin Iii Deficiency
|
|
At Iii Deficiency
|
Congenital At-Iii Deficiency
|
|
Inherited Antithrombin Deficiency
|
Antithrombin 3 Deficiency
|
|
Antithrombin Deficiency
|
Antithrombin-Iii Deficiency
|
|
At-Iii Deficiency
|
Thrombophilia Due To Antithrombin-Iii Deficiency
|
|
|
| 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
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| Hemophilia |
|
Haemophilia
|
Hemophilia, Familial
|
|
Hemophilia, Hereditary
|
Hemophilia A
|
|
Hemophilia, Nos
|
|
|
| Antiphospholipid Syndrome |
|
Antiphospholipid Antibody Syndrome
|
Hughes Syndrome
|
|
Familial Antiphospholipid Syndrome
|
Aps
|
|
Lupus Anticoagulant, Familial
|
Anti-Phospholipid Syndrome
|
|
Apls
|
Classic Apls
|
|
Classic Antiphospholipid Syndrome
|
Acromegaloid Facial Appearance Syndrome
|
|
Anticardiolipin Syndrome
|
|
|
| Thrombosis |
|
Thrombosis Of Blood Vessel
|
|
|
| Thrombophilia |
|
|
| Prothrombin Deficiency, Congenital |
|
Dysprothrombinemia
|
Hypoprothrombinemia
|
|
Congenital Factor Ii Deficiency
|
Prothrombin Deficiency
|
|
Factor Ii Deficiency
|
Congenital Prothrombin Deficiency
|
|
FA2D
|
Hypoprothrombinemias
|
|
Inherited Factor Ii Deficiency
|
Hereditary Factor Ii Deficiency Disease
|
|
|
| Factor V Deficiency |
|
Parahemophilia
|
Labile Factor Deficiency
|
|
Proaccelerin Deficiency
|
Owren Disease
|
|
Owren Parahemophilia
|
Quebec Platelet Disorder
|
|
Deficiency, Labile
|
Hereditary Hypoproaccelerinaemia
|
|
Owren'S Disease
|
Congenital Factor V Deficiency
|
|
FA5D
|
Factor 5 Deficiency
|
|
Deficiency, Factor V
|
|
|
| Thrombophilia Due To Thrombin Defect |
|
Venous Thromboembolism
|
Venous Thrombosis
|
|
Thrombophilia Due To Factor 2 Defect
|
Thromboembolism
|
|
THPH1
|
Thromboembolism, Susceptibility To
|
|
Venous Thromboembolism, Susceptibility To
|
Venous Thrombosis, Protection Against
|
|
Prothrombin-Related Thrombophilia
|
Hyperprothrombinemia
|
|
Venous Thrombosis, Susceptibility To
|
Thrombophilia 1 Due To Thrombin Defect
|
|
F2-Related Thrombophilia
|
Factor Ii-Related Thrombophilia
|
|
Prothrombin 20210g>A Thrombophilia
|
Prothrombin G20210a Thrombophilia
|
|
Prothrombin Thrombophilia
|
|
|
| Factor Vii Deficiency |
|
Hypoproconvertinemia
|
F7 Deficiency
|
|
Congenital Proconvertin Deficiency
|
Congenital Factor Vii Deficiency
|
|
Factor 7 Deficiency
|
Deficiency, Stable
|
|
Proconvertin Deficiency
|
Prothrombin Conversion Accelerator Deficiency
|
|
Serum Prothrombin Conversion Accelerator Deficiency
|
Proconvertin Deficiency, Congenital
|
|
FA7D
|
Stable Disease
|
|
Deficiency, Factor Vii
|
|
|
| Quebec Platelet Disorder |
|
Factor V Quebec
|
QPD
|
|
Bdplt5
|
Bleeding Disorder, Platelet-Type, 5
|
|
Platelet-Type Bleeding Disorder 5
|
Bleeding Disorder Platelet-Type 5
|
|
Platelet Disorder, Quebec
|
|
|
| Thrombophilia Due To Activated Protein C Resistance |
|
Activated Protein C Resistance
|
Apc Resistance
|
|
THPH2
|
Thrombophilia Due To Deficiency Of Activated Protein C Cofactor
|
|
Proc Cofactor Deficiency
|
Pccf Deficiency
|
|
Thrombophilia V
|
Thrombophilia, Susceptibility To, Due To Factor V Leiden
|
|
Thrombophilia Due To Factor V Leiden
|
Thrombophilia 2 Due To Activated Protein C Resistance
|
|
Thrombophilia, Susceptibility To, Due To Activated Protein C Resistance
|
|
|
| Atrial Fibrillation |
|
A-Fib
|
Fibrillation, Atrial
|
|
Af - [Atrial Fibrillation]
|
Rapid Atrial Fibrillation
|
|
A Fib - [Atrial Fibrillation]
|
|
|
| Protein Z Deficiency |
|
|
| Protein S Deficiency |
|
Protein S Deficiency Disease
|
Hereditary Thrombophilia Due To Protein S Deficiency
|
|
|
| Pulmonary Embolism |
|
Pulmonary Artery Embolism
|
Pulmonary Embolus
|
|
Pulmonary Emboli
|
|
|
| Afibrinogenemia, Congenital |
|
Congenital Afibrinogenemia
|
Afibrinogenemia
|
|
Factor I Deficiency
|
Familial Afibrinogenemia
|
|
Hypofibrinogenemia, Congenital
|
Fibrinogen Deficiency
|
|
Afibrinogenemia Congenital
|
CAFBN
|
|
Congenital Hypofibrinogenemia
|
Hypofibrinogenemia
|
|
Complement Factor I Deficiency
|
|
|
| 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
|
|
|
| Glanzmann Thrombasthenia 1 |
|
Glanzmann Thrombasthenia
|
Thrombasthenia Of Glanzmann And Naegeli
|
|
Glanzmann'S Thrombasthenia
|
Bdplt2
|
|
Platelet Glycoprotein Iib-Iiia Deficiency
|
Deficiency Of Platelet Fibrinogen Receptor
|
|
GT1
|
Gt
|
|
Platelet Fibrinogen Receptor Deficiency
|
Glycoprotein Complex Iib-Iiia Deficiency
|
|
Deficiency Of Glycoprotein Complex Iib-Iiia
|
Glycoprotein Iib/Iiia Defect
|
|
Glanzmann Thrombasthenia, Type A
|
Thrombasthenia
|
|
Bleeding Disorder, Platelet-Type, 2
|
Gp Iib-Iiia Complex Deficiency
|
|
Deficiency Of Gp Iib-Iiia Complex
|
Platelet-Type Bleeding Disorder 2
|
|
Thrombocytasthenia
|
Deficiency Of Gp 2b 3a Complex
|
|
Diacyclothrombopathia 2b 3a
|
Glanzmann Thrombasthenia Type A
|
|
Platelet Fibrinogen Receptor, Deficiency Of
|
Platelet Glycoprotein 2b 3a Deficiency
|
|
Glanzmann Disease
|
Glanzmann-Naegeli Disorder
|
|
Hereditary Hemorrhagic Thrombasthenia
|
Hereditary Thrombasthenia
|
|
Bleeding Disorder Platelet-Type 2
|
|
|
| Blood Platelet Disease |
|
Platelet Disorder
|
Blood Platelet Disorders
|
|
Thrombocytopathy
|
Platelet Dysfunction
|
|
Platelet Disorders
|
Qualitative Platelet Deficiency
|
|
|
| Puerperal Pulmonary Embolism |
|
Obstetric Pulmonary Embolism
|
|
|
| Acute Myocardial Infarction |
|
Cardiac Attack
|
Heart Attack
|
|
|
| Viral Hepatitis |
|
Animal Viral Hepatitis
|
Hepatitis, Viral, Animal
|
|
Human Viral Hepatitis
|
Viral Hepatitis With Hepatic Coma
|
|
|
| Pulmonary Artery Disease |
|
Abnormality Of The Pulmonary Artery
|
|
|
| Brachydactyly, Type D |
|
Brachydactyly Type D
|
BDD
|
|
Stub Thumb
|
Brachydactyly D
|
|
|
| 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
|
|
|
| Intracranial Thrombosis |
|
Cerebral Thrombosis
|
Thrombosis Of Cerebral Veins
|
|
Cerebral Arterial Thrombosis
|
|
|
| Gastroduodenal Crohn'S Disease |
|
|
| Post-Thrombotic Syndrome |
|
Postphlebitic Syndrome
|
Postthrombotic Syndrome
|
|
Postphlebetic Syndrome With Inflammation
|
Postphlebetic Syndrome With Ulcer
|
|
Postphlebetic Syndrome With Ulcer And Inflammation
|
Venous Stress Disorder
|
|
|
| Prothrombin Deficiency |
|
Factor Ii Deficiency
|
Hypoprothrombinemia
|
|
Dysprothrombinemia
|
Deficiency, Prothrombin
|
|
Inherited Factor Ii Deficiency
|
Hereditary Factor Ii Deficiency Disease
|
|
|
| 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
|
|
|
| Temporal Lobe Neoplasm |
|
Neoplasm Of Temporal Lobe
|
Malignant Neoplasm Of Temporal Lobe
|
|
Tumor Of Temporal Lobe
|
|
|
| Peroxisome Biogenesis Disorder 11a |
|
PBD11A
|
Peroxisome Biogenesis Disorder Complementation Group 13
|
|
PBD-CG13
|
Cg13
|
|
Pbd-Cgh
|
Peroxisome Biogenesis Disorder Complementation Group H
|
|
Peroxisome Biogenesis Disorder, Type 11a
|
Peroxisome Biogenesis Disorder, Complementation Group 13
|
|
|
| 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
|
|
|
| Stroke, Ischemic |
|
Cerebral Infarction
|
Stroke
|
|
Ischemic Stroke
|
Cerebrovascular Accident
|
|
Cerebral Infarction, Susceptibility To
|
Stroke, Ischemic, Susceptibility To
|
|
Cerebral Infarct
|
Ischemic Stroke, Susceptibility To
|
|
Stroke, Susceptibility To
|
Cva - Cerebral Infarction
|
|
ISCHSTR
|
Ischemic Cerebrovascular Accident
|
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| Alpha-2-Plasmin Inhibitor Deficiency |
|
Plasmin Inhibitor Deficiency
|
Antiplasmin Deficiency
|
|
Antiplasmin Defiency
|
Anti-Plasmin Deficiency, Congenital
|
|
Antiplasmin Deficiency, Congenital
|
Congenital Alpha2-Antiplasmin Deficiency
|
|
APLID
|
Congenital Alpha2 Antiplasmin Deficiency
|
|
|
| Lipoprotein Quantitative Trait Locus |
|
Coronary Artery Disease
|
Coronary Artery Anomaly
|
|
Coronary Artery Disease, Susceptibility To
|
Myocardial Ischemia
|
|
Congenital Anomaly Of Coronary Artery
|
Coronary Arteriosclerosis
|
|
Coronary Disease
|
Coronary Heart Disease
|
|
Coronary Artery Disorder
|
LPAQTL
|
|
Lpa Deficiency, Congenital
|
Coronary Artery Abnormality
|
|
Coronary Artery Anomaly, Congenital
|
Chd
|
|
Coronary Syndrome
|
Congenital Malformations Of Coronary Vessels
|
|
Malformation Of Coronary Vessels
|
Congenital Coronary Artery Anomaly
|
|
Congenital Coronary Artery Deformity
|
Congenital Coronary Artery Disorder
|
|
Abnormal Coronary Artery
|
Congenital Coronary Artery Malposition
|
|
Congenital Coronary Disease
|
Congenital Anomaly Of Coronary Arteries
|
|
|
| Patent Foramen Ovale |
|
Atrial Septal Defect Within Oval Fossa
|
Foramen Ovale Patent
|
|
Ostium Secundum Atrial Septal Defect
|
Atrial Septal Defect, Ostium Secundum Type
|
|
Foramen Ovale, Patent
|
Defect, Patent Or Persistent, Ostium Secundum
|
|
Ostium Secundum Type Atrial Septal Defect
|
Persistent Ostium Secundum
|
|
Asd Ostium Secundum Type
|
Ostium Secundum Asd
|
|
Osasd
|
Asd, Ostium Secundum Type
|
|
Pfo - [Patent Foramen Ovale]
|
Open Foramen Ovale
|
|
Open Oval Foramen
|
Persistent Foramen Ovale
|
|
Secundum Atrial Septal Defect
|
|
|
