| Diseases |
Alias |
|
| 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
|
|
|
| Carotid Artery Thrombosis |
|
|
| 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
|
|
|
| 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
|
|
|
| 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 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
|
|
|
| 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
|
|
|
| Heparin-Induced Thrombocytopenia |
|
Hit
|
Hat
|
|
Heparin-Associated Thrombocytopenia
|
Heparin-Induced Thrombocytopenia Type 2
|
|
|
| Covid-19 |
|
2019 Novel Coronavirus
|
2019-Ncov Infection
|
|
Covid19
|
Sars-Cov-2 Infection
|
|
Wuhan Coronavirus Infection
|
Wuhan Seafood Market Pneumonia Virus Infection
|
|
|
| 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
|
|
|
| Pulmonary Embolism |
|
Pulmonary Artery Embolism
|
Pulmonary Embolus
|
|
Pulmonary Emboli
|
|
|
| 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
|
|
|
| Hantavirus Pulmonary Syndrome |
|
Hps
|
Four Corners Hantavirus
|
|
Hards
|
Hantavirus
|
|
Hantavirus-Associated Respiratory Distress Syndrome
|
Hanta Virus
|
|
Hantavirus Cardiopulmonary Syndrome
|
Hps - [Hantavirus Pulmonary Syndrome]
|
|
Hcps - [Hantavirus Cardiopulmonary Syndrome]
|
|
|
| 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
|
|
|
| Intracranial Hypertension |
|
Raised Intracranial Pressure
|
|
|
| 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
|
|
|
| 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
|
|
|
| Pulmonary Artery Disease |
|
Abnormality Of The Pulmonary Artery
|
|
|
| Afibrinogenemia, Congenital |
|
Congenital Afibrinogenemia
|
Afibrinogenemia
|
|
Factor I Deficiency
|
Familial Afibrinogenemia
|
|
Hypofibrinogenemia, Congenital
|
Fibrinogen Deficiency
|
|
Afibrinogenemia Congenital
|
CAFBN
|
|
Congenital Hypofibrinogenemia
|
Hypofibrinogenemia
|
|
Complement Factor I Deficiency
|
|
|
| Thrombotic Thrombocytopenic Purpura |
|
Purpura, Thrombotic Thrombocytopenic
|
Ttp
|
|
Thrombotic Thrombocytopenic Purpura, Acquired
|
Idiopathic Thrombotic Thrombocytopenic Purpura
|
|
Moschcowitz Disease
|
Moschcowitz'S Syndrome
|
|
Moschowitz Syndrome
|
Chronic Relapsing Thrombotic Thrombocytopenic Purpura
|
|
Familial Thrombotic Thrombocytopenia Purpura
|
Moschkowitz Disease
|
|
Purpura Thrombotic Thrombocytopenic
|
Familial Thrombotic Thrombocytopenic Purpura
|
|
Microangiopathic Hemolytic Anemia
|
Congenital Thrombotic Thrombocytopenic Purpura
|
|
Autoimmune Thrombotic Thrombocytopenic Purpura
|
Ttp - [Thrombotic Thrombocytopenic Purpura]
|
|
Moschcowitz Syndrome
|
|
|
| Protein S Deficiency |
|
Protein S Deficiency Disease
|
Hereditary Thrombophilia Due To Protein S Deficiency
|
|
|
| Thrombophilia |
|
|
| Sagittal Sinus Thrombosis |
|
Thrombosis Of Superior Longitudinal Sinus
|
Thrombosis Of Superior Sagittal Sinus
|
|
Thrombosis Superior Sagittal Sinus
|
|
|
| Thrombosis |
|
Thrombosis Of Blood Vessel
|
|
|
| Liver Disease |
|
Liver Failure
|
Liver Diseases
|
|
Abnormality Of The Liver
|
Liver Dysfunction
|
|
Disorder Of Liver
|
Hepatic Disorder
|
|
Hepatic Disease
|
Disease Of Bilirubin Metabolism
|
|
Disorder Of Bilirubin Metabolism
|
Liver Decompensation
|
|
Liver Function Failure
|
Hepatic Failure Nos
|
|
Liver Failure Nos
|
End Stage Liver Disease
|
|
Decompensated Liver Failure
|
Decompensation Of Liver Function
|
|
Hepatic Decompensation
|
Hepatic Insufficiency
|
|
Liver Cell Necrosis With Hepatic Failure
|
Liver Insufficiency
|
|
Decompensated Liver Disease
|
End Stage Liver Failure
|
|
Liver Necrosis With Hepatic Failure
|
|
|
| Nonbacterial Thrombotic Endocarditis |
|
Non-Bacterial Thrombotic Endocarditis
|
Marantic Endocarditis
|
|
Non-Infective Endocarditis
|
|
|
| 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
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| Scrub Typhus |
|
Tsutsugamushi Disease
|
Tsutsugamushi Fever
|
|
Typhus Fever Due To Rickettsia Tsutsugamushi
|
Chigger-Borne Rickettsiosis
|
|
Chigger-Borne Typhus
|
Japanese River Fever
|
|
Kedani Fever
|
Mite-Borne Rickettsiosis
|
|
Mite-Borne Typhus
|
Scrub Typhus
|
|
Scrub Mite-Borne Typhus
|
Tropical Typhus
|
|
Tsutsugamushi
|
|
|
| Intracranial Thrombosis |
|
Cerebral Thrombosis
|
Thrombosis Of Cerebral Veins
|
|
Cerebral Arterial Thrombosis
|
|
|
| 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
|
|
|
| Thrombocytosis |
|
|
| Blood Platelet Disease |
|
Platelet Disorder
|
Blood Platelet Disorders
|
|
Thrombocytopathy
|
Platelet Dysfunction
|
|
Platelet Disorders
|
Qualitative Platelet Deficiency
|
|
|
| Hepatic Veno-Occlusive Disease |
|
Veno-Occlusive Disease
|
Sinusoidal Obstruction Syndrome
|
|
Hepatic Venoocclusive Disease
|
Venoocclusive Disease
|
|
Hepatic Vein Thrombosis
|
Budd-Chiari Syndrome
|
|
Hepatic Vein Occlusion
|
Veno-Occlusive Disease Of The Liver
|
|
|
| Purpura Fulminans |
|
|
| Acute Myocardial Infarction |
|
Cardiac Attack
|
Heart Attack
|
|
|
| Purpura |
|
|
| Prothrombin Deficiency |
|
Factor Ii Deficiency
|
Hypoprothrombinemia
|
|
Dysprothrombinemia
|
Deficiency, Prothrombin
|
|
Inherited Factor Ii Deficiency
|
Hereditary Factor Ii Deficiency Disease
|
|
|
| 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
|
|
|
| Coronary Thrombosis |
|
Coronary Artery Thrombosis
|
|
|
| Budd-Chiari Syndrome |
|
Hepatic Vein Thrombosis
|
Chiari Syndrome
|
|
BDCHS
|
Membranous Obstruction Of The Inferior Vena Cava
|
|
Budd-Chiari Syndrome, Somatic
|
Movc
|
|
Budd-Chiari Syndrome, Susceptibility To, Somatic
|
Budd-Chiari Syndrome, Susceptibility To
|
|
Membranous Obstruction Of Inferior Vena Cava
|
Hepatic Vein Block
|
|
Obstruction Of Hepatic Veins
|
Hepatic Vein Obstruction
|
|
Hepatic Venous Block
|
|
|
| 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
|
|
|
| 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
|
|
|
| Achenbach Syndrome |
|
Paroxysmal Hematoma Of The Finger
|
|
|
| Hemolytic-Uremic Syndrome |
|
Hemolytic Uremic Syndrome
|
Haemolytic-Uraemic Syndrome
|
|
Hus
|
Acute Renal Failure, Thrombocytopenia, And Microangiopathic Hemolytic Anemia Associated With Distorted Erythrocytes
|
|
Typical Haemolytic Uraemic Syndrome
|
Gasser Syndrome
|
|
Hus - [Haemolytic Uraemic Syndrome]
|
|
|
| Qualitative Platelet Defect |
|
Qualitative Platelet Defects
|
Qualitative Platelet Deficiency
|
|
Thrombocytopathy
|
Platelet Defect
|
|
Platelet Disorder
|
Thrombopathy
|
|
Platelet Granule Defect
|
Thrombocytasthenia
|
|
Thromboasthenia
|
Dystrophic Thrombocytopathy
|
|
Haemorrhagic Thrombasthenia
|
Granulopenic Thrombocytopathy
|
|
|
| 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
|
|
|
| Chronic Urticaria |
|
Urticaria Chronic
|
Chronic Spontaneous Urticaria
|
|
Chronic Ordinary Urticaria
|
|
|
| Pyoderma |
|
|
| Femoral Neuropathy |
|
Femoral Nerve Dysfunction
|
Femoral Nerve Lesions
|
|
|
| Monocytic Leukemia |
|
Monocytic Leukaemia
|
Schilling'S Leukaemia
|
|
Schilling'S Leukemia
|
M5b Acute Differentiated Monocytic Leukemia
|
|
|
| Placental Insufficiency |
|
Uteroplacental Vascular Insufficiency
|
|
|
| Compartment Syndrome |
|
Compartment Syndromes
|
Compartmental Syndrome
|
|
|
| Intracranial Embolism |
|
Cerebral Embolism
|
Cerebral Embolism With Cerebral Infarction
|
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
| Retinal Vein Occlusion |
|
Occlusion, Of Retinal Vein
|
|
|
| Hepatitis A |
|
Viral Hepatitis A
|
Viral Hepatitis, Type A
|
|
|
| Buruli Ulcer |
|
Buruli Ulcer, Susceptibility To
|
Buruli Ulcer Disease
|
|
Mycobacterium Ulcerans
|
Mycobacterium Ulcerans, Susceptibility To
|
|
Bairnsdale Ulcer
|
Daintree Ulcer
|
|
Mossman Ulcer
|
Searl Ulcer
|
|
Searle'S Ulcer
|
Bud
|
|
|
| Pyoderma Gangrenosum |
|
Phagedenic Pyoderma
|
Phagedena Geometric
|
|
|
| Angina Pectoris |
|
Prinzmetal'S Variant Angina
|
Angina
|
|
Prinzmetal Angina
|
Variant Angina
|
|
Angina Inversa
|
Prinzmetal'S Angina
|
|
Coronary Artery Vasospasm
|
Angina Pectoris, Variant
|
|
Variant Angina Pectoris
|
Vasospastic Angina
|
|
Angor Pectoris
|
Anginal Syndrome
|
|
Ischaemic Chest Pain
|
Angina Pectoris Syndrome
|
|
Angina Syndrome
|
Cardiac Angina Syndrome
|
|
Ap - [Angina Pectoris]
|
Angina Nos
|
|
Ap - [Angina Pectoris] Syndrome
|
Ischaemic Heart Disease With Angina
|
|
Heart Angina
|
Chest Angina
|
|
Angina Attack
|
Anginal Cardiopathy
|
|
Coronary Pain Nos
|
|
|
| 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
|
|
|
| Acquired Von Willebrand Syndrome |
|
Acquired Von Willebrand Disease
|
Willebrand Disease, Acquired
|
|
Avws
|
|
|
| Hemopneumothorax |
|
|
| Hellp Syndrome |
|
Hemolysis, Elevated Liver Enzymes, Lowered Platelets
|
Hemolysis, Elevated Liver Enzymes, Low Platelets In Pregnancy
|
|
Hemolysis-Elevated Liver Enzymes-Low Platelets Syndrome
|
Hellp - [Syndrome Of Haemolysis, Elevated Liver Enzymes And Low Platelet]
|
|
Haemolysis-Elevated Liver Enzymes-Low Platelet Count Syndrome
|
|
|
| Acute Cor Pulmonale |
|
|
| Acute Promyelocytic Leukemia |
|
Leukemia, Acute Promyelocytic
|
Acute Myeloblastic Leukemia Type 3
|
|
Aml M3
|
APL
|
|
Leukemia, Acute Promyelocytic, Somatic
|
Aml With T(15
|
|
17)(Q22
|
Q12)
|
|
(Pml/Raralpha) And Variants
|
Apml
|
|
Acute Myeloblastic Leukemia 3
|
Acute Myeloid Leukemia With T(15
|
|
17)(Q22
|
Q12)
|
|
(Pml/Raralpha) And Variants
|
Acute Myeloblastic Leukaemia Type 3
|
|
Acute Myeloid Leukaemia M3
|
Acute Myeloid Leukemia M3
|
|
Acute Promyelocytic Leukaemia
|
M3 Anll
|
|
Myeloid Leukemia, Acute, M3
|
Leukemia Promyelocytic Acute
|
|
Leukemia, Promyelocytic, Acute
|
Leukemia, Acute, Promyelocytic
|
|
|
| Crimean-Congo Hemorrhagic Fever |
|
Crimean Hemorrhagic Fever
|
Cchf
|
|
Congo Hemorrhagic Fever
|
Hemorrhagic Fever, Crimean
|
|
Chf Congo Virus
|
Congo-Crimean Hemorrhagic Fever
|
|
Congo Fever
|
Hemorrhagic Fever Crimean-Congo
|
|
Cchf - [Crimean-Congo Haemorrhagic Fever]
|
Kara Mikh Typhoid Fever
|
|
Xīnjiāng Haemorrhagic Fever
|
|
|
| Intracranial Sinus Thrombosis |
|
Sinus Thrombosis, Intracranial
|
|
|
| Giant Hemangioma |
|
|
| Hemopericardium |
|
Haemopericardium
|
Pericardial Effusion
|
|
Haematopericardium
|
Pneumohemopericardium
|
|
Pericardium Haemorrhage
|
Haemorrhagic Pericarditis
|
|
|
| Erythema Multiforme |
|
Dermatostomatitis, Erythema Multiforme Type
|
Em
|
|
Erythema Multiforme Bullosum
|
Erythema Polymorphe, Erythema Multiforme Type
|
|
Febrile Mucocutaneous Syndrome
|
Herpes Iris, Erythema Multiforme Type
|
|
Stevens-Johnson Syndrome
|
Em - [Erythema Multiforme]
|
|
|
| Liver Cirrhosis |
|
Cirrhosis
|
Cirrhosis Of Liver
|
|
CIRRH
|
Cryptogenic Cirrhosis
|
|
Cirrhosis, Cryptogenic
|
Cirrhosis Nos
|
|
|
| Vein Disease |
|
|
| Cavernous Sinus Thrombosis |
|
Thrombosis Of Cavernous Venous Sinus
|
|
|
| Placenta Disease |
|
Placenta Diseases
|
Placenta Disorder
|
|
Pregnancy Complications
|
Placenta Disorders
|
|
|
| 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
|
|
|
| Hemolytic Anemia |
|
Anemia, Hemolytic
|
Anemia Hemolytic
|
|
Anaemia Due To Other Disorders Of Glutathione Metabolism
|
Chronic Non Spherocytic Anaemia
|
|
G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia
|
Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency
|
|
Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia
|
Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia
|
|
Favism Anaemia
|
Haemolytic Anaemia Due Tog6pd Deficiency
|
|
Favism
|
Pentose Phosphate Pathway Disorder Anaemia
|
|
Anaemia Due To Pentose Phosphate Pathway Defect
|
|
|
| Post-Thrombotic Syndrome |
|
Postphlebitic Syndrome
|
Postthrombotic Syndrome
|
|
Postphlebetic Syndrome With Inflammation
|
Postphlebetic Syndrome With Ulcer
|
|
Postphlebetic Syndrome With Ulcer And Inflammation
|
Venous Stress Disorder
|
|
|
| Pre-Eclampsia |
|
Preeclampsia
|
Gestational Hypertension
|
|
Hypertension Induced By Pregnancy
|
Pre-Eclamptic Toxaemia
|
|
Pregnancy Associated Hypertension
|
Proteinuric Hypertension Of Pregnancy
|
|
Hypertension, Pregnancy-Induced, Susceptibility To
|
Preeclampsia/Eclampsia
|
|
Pregnancy Toxemia
|
Toxaemia Of Pregnancy
|
|
Gestational Proteinuric Hypertension
|
Pregnancy-Induced Hypertension
|
|
Toxemia Of Pregnancy
|
Preeclampsia, Susceptibility To
|
|
Transient Hypertension Of Pregnancy
|
Gestational [Pregnancy-Induced] Hypertension Without Significant Proteinuria
|
|
Gestational Hypertension Nos
|
Mild Proteinuric Hypertension Of Pregnancy
|
|
Pih - [Pregnancy-Induced Hypertension]
|
Pregnancy-Induced Hypertension Nos
|
|
Gestational [Pregnancy-Induced] Hypertension With Significant Proteinuria
|
Pe - [Pre-Eclampsia]
|
|
Pre-Eclampsia Nos
|
Pre-Eclamptic Nos
|
|
Pregnancy Pre-Eclampsia
|
Puerperal Pre-Eclampsia
|
|
Pre-Eclampsia Toxaemia
|
Toxaemia In Pregnancy
|
|
Pet - [Pre-Eclamptic Toxaemia]
|
Maternal Toxaemia
|
|
|
| Waterhouse-Friderichsen Syndrome |
|
Fatal Pneumococcal Waterhouse-Friderichsen Syndrome
|
Meningococcal Hemorrhagic Adrenalitis
|
|
Waterhouse-Friderichsen Syndrome, Meningococcal
|
Meningococcal Haemorrhagic Adrenalitis
|
|
Meningococcal Adrenal Syndrome
|
Acute Adrenal Insufficiency With Meningococcal Septicaemia
|
|
Adrenal Haemorrhage Syndrome
|
Waterhouse-Friderichsen Disease
|
|
Meningococcal Waterhouse-Friderichsen Syndrome
|
Haemorrhagic Meningococcal Adrenitis
|
|
|
| Acute Pulmonary Heart Disease |
|
|
| Autoimmune Disease Of Cardiovascular System |
|
|
| Splenic Infarction |
|
Splenic Infarct
|
Splenic Infarcts
|
|
Infarct Of The Spleen
|
|
|
| Arteriosclerosis |
|
Arteriosclerotic Vascular Disease
|
|
|
| Subclavian Steal Syndrome |
|
Subclavian Artery Stenosis
|
Subclavian Steal Phenomenon
|
|
Subclavian Steal Steno-Occlusive Disease
|
Subclavian Steal
|
|
|
| Nephrosclerosis |
|
|
| Shwartzman Phenomenon |
|
|
| Eclampsia |
|
Eclampsia In Puerperium
|
Postpartum Eclampsia
|
|
Eclampsia, Postpartum
|
Puerperal Eclampsia
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Active Peptic Ulcer Disease |
|
Gi Bleeding
|
Active Peptic Ulcer
|
|
Gastrointestinal Hemorrhage
|
|
|
| Synovial Angioma |
|
Hemangioma Of Synovium
|
Synovial Hemangioma
|
|
|
| Toxic Shock Syndrome |
|
Septic Shock
|
Toxic Shock
|
|
Tss
|
Shock, Septic
|
|
Staphylococcal Toxic Shock Syndrome
|
Tss - [Toxic Shock Syndrome]
|
|
|
| Peripheral Vascular Disease |
|
Peripheral Arterial Disease
|
Arterial Occlusive Disease
|
|
Arterial Occlusive Diseases
|
Pad
|
|
Peripheral Vascular Diseases
|
Peripheral Occlusive Disease
|
|
Peripheral Arterial Diseases
|
Helicobacter Infections
|
|
|
| Hepatic Vascular Disease |
|
Vascular Disorder Of Liver
|
|
|
| Lemierre'S Syndrome |
|
Lemierre Syndrome
|
Lemierre Postanginal Sepsis
|
|
Necrobacillosis
|
Postanginal Sepsis Secondary To Orophyngeal Infection
|
|
Septic Phlebitis Of The Internal Jugular Vein
|
Fusobacterium Infections
|
|
Acute Sore Throat
|
Human Necrobacillosis
|
|
Postanginal Sepsis
|
Oropharyngeal Infection Leading To Secondary Septic Thrombophlebitis Of The Internal Jugular Vein
|
|
|
| Atrial Fibrillation |
|
A-Fib
|
Fibrillation, Atrial
|
|
Af - [Atrial Fibrillation]
|
Rapid Atrial Fibrillation
|
|
A Fib - [Atrial Fibrillation]
|
|
|
| Endocardium Disease |
|
|
| Pericardium Disease |
|
|
| Pulmonary Hypertension |
|
Primary Pulmonary Hypertension
|
Hypertension Pulmonary
|
|
Hypertension, Pulmonary
|
Hypertension, Pulmonary, Primary
|
|
Idiopathic Pulmonary Hypertension
|
Idiopathic Pulmonary Arterial Hypertension
|
|
Pulmonary Htn - [Hypertension]
|
|
|
| Severe Acute Respiratory Syndrome |
|
Sars
|
Sars-Cov Infection
|
|
Sars-1
|
Sar Deficiency
|
|
Sars - [Severe Acute Respiratory Syndrome]
|
|
|
| Vitamin K Deficiency Bleeding |
|
Vitamin K Deficiency
|
Deficiency Of Vitamin K
|
|
Vitamin K
|
Vitamin K Deficiency Hemorrhagic Disease
|
|
|
| Cardiac Tamponade |
|
Pericardial Tamponade
|
Rose'S Tamponade
|
|
|
| Primary Thrombocytopenia |
|
|
| Esophageal Varix |
|
Esophageal Varices
|
Bleeding Esophageal Varices
|
|
Bleeding Oesophageal Varices
|
Esophageal Varices In Disease Classified Elsewhere, With Bleeding
|
|
Esophageal Varices With Bleeding
|
Esophageal Varices With Bleeding In Disease Ec
|
|
Esophageal Varices Without Bleeding
|
Esophageal Varices Without Mention Of Bleeding
|
|
|
| Cholangitis |
|
Acute Cholangiolitis
|
Ascending Cholangitis
|
|
Cholangiolitis
|
Cholangitis Nos
|
|
Chronic Cholangiolitis
|
Hepatic Duct Inflammation
|
|
Acute Cholangitis
|
Bile Duct Inflammation
|
|
|
| Polycythemia |
|
Erythrocythemia
|
Polycythemia Vera
|
|
Polycythaemia Due To High Altitude
|
|
|
| Myocarditis |
|
Myocardial Inflammation
|
Inflammatory Cardiomyopathy
|
|
|
| Hemangioma |
|
|
| 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
|
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| Epidural Abscess |
|
|
| Infective Endocarditis |
|
Bacterial Endocarditis
|
Endocarditis, Infective
|
|
Infectious Endocarditis
|
Endocarditis Infective
|
|
|
| Systemic Lupus Erythematosus |
|
Lupus Nephritis
|
SLE
|
|
Disseminated Lupus Erythematosus
|
Systemic Lupus Erythematosus, Susceptibility To
|
|
Lupus Erythematosus, Systemic
|
Lupus Nephritis, Susceptibility To
|
|
Libman-Sacks Disease
|
Systemic Lupus Erythematosus Susceptibility To
|
|
Sle - Lupus Erythematosus, Systemic
|
Le Syndrome
|
|
Lupus
|
Lupus Erythematosus Systemic
|
|
Lupus Erythematosus, Systemic, Susceptibility To
|
Lupus Vulgaris
|
|
Lupus Erythematosus, Discoid
|
Lupus Erythematosus
|
|
Systemic Lupus Erythematosus Nos
|
Sle - [Systemic Lupus Erythematosus]
|
|
|
| Emphysematous Cholecystitis |
|
Gaseous Pericholecystitis
|
|
|
| Aortic Aneurysm |
|
Aortic Rupture
|
Thoracoabdominal Aortic Aneurysm, Ruptured
|
|
Ruptured Aortic Aneurysm
|
Aortic Aneurysms
|
|
Aortic Aneurysm Without Mention Of Rupture Nos
|
Ruptured Abdominal Aortic Aneurysm
|
|
Aortic Aneurysm, Ruptured
|
Ruptured Thoracic Aortic Aneurysm
|
|
|
| Intracranial Hypotension |
|
|
| Portal Vein Thrombosis |
|
Phlebitis Of Portal Vein
|
Deep Vein Thrombosis Of Portal Vein
|
|
Portal Thrombosis
|
Pvt - [Portal Vein Thrombosis]
|
|
Portal Venous Thrombosis
|
Portal Venous Embolism
|
|
Portal Venous Obstruction
|
Portal Venous Block
|
|
Portal Vein Embolism
|
Portal Vein Block
|
|
Portal Obstruction
|
Portal Embolism
|
|
Portal Block
|
Hepatic Portal Vein Obstruction
|
|
Occlusion Of Hepatic Portal Vein
|
Portal Vein Obstruction
|
|
|
| Thrombophlebitis |
|
Phlebitis And Thrombophlebitis Of Superficial Vessels Of Lower Extremities
|
Superficial Thrombophlebitis Of Leg
|
|
Thrombophlebitis Of A Superficial Leg Vein
|
Thrombophlebitis Of Superficial Veins Of Lower Extremity
|
|
|
| Bacterial Sepsis |
|
|
| Thrombasthenia |
|
|
| Polycythemia Vera |
|
PV
|
Polycythemia Rubra Vera
|
|
Prv
|
Osler-Vaquez Disease
|
|
Chronic Erythremia
|
Polycythaemia Rubra Vera
|
|
Primary Polycythemia
|
Vaquez Disease
|
|
Polycythemia Vera, Somatic
|
Osler-Vaquez Syndrome
|
|
Proliferative Polycythaemia
|
Polycythemia Ruba Vera
|
|
Acquired Primary Erythrocytosis
|
Heilmeyer-Schoner Disease
|
|
Vaquez Osler Disease
|
Primary Polycythaemia
|
|
|
| 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
|
|
|
| Speech And Communication Disorders |
|
Language Disorder
|
Communication Disorder
|
|
Language Disorders
|
Communication Disorders
|
|
Speech Language Disorder
|
Speech-Language Disorder
|
|
Communication Impairment
|
Speech And Language Disorder
|
|
|
| Atherosclerosis Susceptibility |
|
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
|
Alp
|
Arteriosclerosis
|
|
|
| Splenic Sequestration |
|
|
| Hepatic Infarction |
|
Infarct Of Liver
|
Hepatic Infarct
|
|
Liver Infarct
|
Liver Infarction
|
|
|
| Von Willebrand Disease, Type 1 |
|
Von Willebrand Disease Type 1
|
VWD1
|
|
Von Willebrand'S Disease 1
|
Von Willebrand Disease Type I
|
|
Von Willebrand Disease, Type I
|
Vwd, Type 1
|
|
Vwd Type 1
|
Von Willebrand Disease 1
|
|
Von Willebrand Factor Deficiency Type 1
|
Von Willebrand Disease, Type 1, Susceptibility To
|
|
|
| Ureteric Orifice Cancer |
|
Malignant Neoplasm Of Ureteric Orifice Of Urinary Bladder
|
Malignant Tumor Of Ureteric Orifice
|
|
Orifice Of The Ureter
|
|
|
| Hepatic Coma |
|
Hepatic Encephalopathy
|
Hepatocerebral Intoxication
|
|
|
| Non-Severe Covid-19 |
|
|
| Brachydactyly, Type D |
|
Brachydactyly Type D
|
BDD
|
|
Stub Thumb
|
Brachydactyly D
|
|
|
| Splenic Abscess |
|
|
| Vertical Talus, Congenital |
|
Congenital Vertical Talus
|
CVT
|
|
Congenital Convex Pes Valgus
|
Rocker-Bottom Foot Deformity
|
|
Vertical Talus
|
Pes Valgus, Congenital Convex
|
|
Congenital Convex Foot
|
Congenital Rocker-Bottom Foot
|
|
Rocker Bottom Foot
|
Flatfoot
|
|
Rocker-Bottom Foot
|
Charcot-Marie-Tooth Disease, Foot Deformity Of
|
|
|
| Malaria |
|
Malaria, Susceptibility To
|
Malaria, Resistance To
|
|
Malaria, Cerebral
|
Cerebral Malaria
|
|
Malaria, Severe, Susceptibility To
|
Malaria, Severe, Resistance To
|
|
Malaria, Cerebral, Susceptibility To
|
Induced Malaria
|
|
Malaria, Vivax, Protection Against
|
Malaria, Severe
|
|
Malaria, Cerebral, Reduced Risk Of
|
Malaria, Protection Against
|
|
Resistance To Malaria Due To G6pd Deficiency
|
Malaria Due To G6pd Deficiency
|
|
Malarial Encephalitis
|
CM
|
|
Malaria Cerebral
|
Susceptibility To Malaria
|
|
Acute Pernicious Fever
|
Aestivo-Autumnal Fever
|
|
Aestivo Autumnal Malaria
|
Chagres Fever
|
|
Continued Malaria Fever
|
Estivo-Autumnal Fever
|
|
Estivo-Autumnal Malaria
|
Estivo-Autumnal Malarial Fever
|
|
Falciparum Fever
|
Malignant Tertian Fever
|
|
Malignant Tertian Malaria
|
Pernicious Intermittent Fever
|
|
Pernicious Malaria
|
Quotidian Malaria
|
|
Subtertian Fever
|
Subtertian Malaria Fever
|
|
Subtertian Malignant Tertian Malaria
|
Tropical Malaria
|
|
Algid Malaria
|
Bilious Haemoglobinuric Fever
|
|
Black Water Fever
|
Blackwater Fever
|
|
Malarial Blackwater Fever
|
Severe Malarial Falciparum
|
|
West African Fever
|
Malarial Haematinuria
|
|
Haemoglobinuric Fever
|
Haemoglobinuric Malaria
|
|
Severe Plasmodium Falciparum Malaria
|
Malarial Haemoglobinuria
|
|
Malarial Haematuria
|
Falciparum Malaria [Malignant Tertian]
|
|
Malaria Tropica
|
Malarial Shock
|
|
Chagres Virus Disease
|
Malignant Malaria
|
|
Mtm - [Malignant Tertian Malaria]
|
Tm -[Malignant Tertian Malaria]
|
|
Panama Fever
|
St - [Subtertian Malaria]
|
|
Malarial Quotidian
|
Benign Tertian Malaria
|
|
Tertian Ague
|
Vivax Fever
|
|
Plasmodium Vivax Malaria Nos
|
Btm - [Benign Tertian Malaria]
|
|
Bt - [Benign Tertian Malaria]
|
Vivax Malaria
|
|
Benign Tertian Vivax Malaria
|
Tertian Malaria
|
|
Quartan Malaria
|
Quartan Ague
|
|
Quartan Fever
|
Plasmodium Malariae Malaria Nos
|
|
Quartan Malarial
|
Malaria By Plasmodium Malariae
|
|
Malariae Malaria
|
Ovale Tertian Malaria
|
|
Plasmodium Ovale Fever
|
Malaria Fever By Plasmodium Ovale
|
|
Ovale Malaria
|
Malaria By Plasmodium Ovale
|
|
Malarial Ovale
|
Marsh Fever
|
|
Remittent Congestive Fever
|
Coastal Fever
|
|
Remittent Gastric Fever
|
Miasmatic Fever
|
|
Congestive Remittent Fever
|
Intermittent Fever
|
|
Jungle Fever
|
Paludism
|
|
Cameroon Fever
|
Ague
|
|
Corsican Fever
|
Intermittent Bilious Fever
|
|
Disease Due To Plasmodiidae
|
Malarial Fever
|
|
Plasmodiosis
|
Remittent Fever
|
|
Roman Fever
|
Malaria Fever Nos
|
|
Malaria Nos
|
Paludal Fever
|
|
Clinically Diagnosed Malaria
|
Clinically Diagnosed Malaria Without Parasitological Confirmation
|
|
Congestive Fever
|
Malarial Cachexia
|
|
Marsh Cachexia
|
Paludal Cachexia
|
|
Recurrent Malaria
|
Remittent Malaria
|
|
|
| Papilledema |
|
Choked Disk
|
Edema Of The Optic Disc
|
|
|
| Blue Toe Syndrome |
|
|
| Coronavirus Infectious Disease |
|
|
| Carotid Artery Disease |
|
Carotid Artery Diseases
|
Disorder Of Carotid Artery
|
|
|
| Leech Infestation |
|
|
| Placental Abruption |
|
Abruptio Placentae
|
Abruptio Placenta
|
|
Abortion, Threatened
|
Threatened Miscarriage
|
|
Haemorrhage Specified As Due To Threatened Abortion
|
Spontaneous Threatened Abortion
|
|
|
| Tricuspid Valve Disease |
|
Rheumatic Tricuspid Valve Disease
|
Disease Of Tricuspid Valve
|
|
Rh. Tricuspid Valve Disease
|
Rheumatic Disease Of Tricuspid Valve
|
|
Tricuspid Disease
|
Tricuspid Valve Disorder
|
|
|
| Severe Covid-19 |
|
|
| Intermediate Coronary Syndrome |
|
Unstable Angina
|
Angina At Rest
|
|
Anginal Chest Pain At Rest
|
Impending Infarction
|
|
Preinfarction Angina
|
Worsening Angina
|
|
Angina, Unstable
|
Myocardial Preinfarction Syndrome
|
|
Angina Unstable
|
Crescendo Angina
|
|
Angina Decubitus
|
Acute Coronary Insufficiency
|
|
Unstable Angina Pectoris
|
Preinfarctional Angina Pectoris
|
|
Worsening Effort Angina
|
Preinfarction Syndrome
|
|
Unstable Angina Pectoris Syndrome
|
Unstable Anginal Attack
|
|
Unstable Cardiac Angina
|
Unstable Chest Angina
|
|
Unstable Heart Angina
|
De Novo Effort Angina Pectoris
|
|
Crescendo Angina Pectoris
|
Ua - [Unstable Angina]
|
|
|
| Anuria |
|
Suppression Of Urinary Secretion
|
|
|
| Autoimmune Disease Of Blood |
|
|
| Central Retinal Artery Occlusion |
|
|
| Occlusion Precerebral Artery |
|
Occlusion And Stenosis Of Multiple And Bilateral Precerebral Arteries
|
Occlusion And Stenosis Of Precerebral Artery
|
|
|
| Angioedema, Hereditary, 3 |
|
Angioedema, Hereditary, Type Iii
|
Hereditary Angioedema Type Iii
|
|
Hereditary Angioedema Type 3
|
HAE3
|
|
Estrogen-Related Hae
|
Estrogen-Sensitive Hae
|
|
Angioneurotic Edema, Hereditary, With Normal C1 Inhibitor Concentration And Function
|
Hae With Normal C1 Inhibitor Concentration And Function
|
|
Hereditary Angioedema With Normal C1 Inhibitor Activity
|
F12-Related Hereditary Angioedema With Normal C1inh
|
|
F12-Related Hae With Normal C1 Inhibitor
|
Hae 3
|
|
Hae-Iii
|
Hereditary Angioneurotic Edema Type 3
|
|
Inherited Estrogen-Associated Angioedema
|
Inherited Estrogen-Associated Angioneurotic Edema
|
|
Inherited Estrogen-Dependent Angioedema
|
Inherited Estrogen-Dependent Angioneurotic Edema
|
|
Angioneurotic Edema Hereditary With Normal C1 Inhibitor Concentration And Function
|
Hereditary Angioedema With Normal C1 Esterase Inhibitor Activity
|
|
|
| Chronic Venous Insufficiency |
|
|
| Branch Retinal Artery Occlusion |
|
Retinal Artery Occlusion
|
Arterial Retinal Branch Occlusion
|
|
Retinal Arterial Branch Occlusion
|
|
|
| Pericardial Effusion |
|
Noninflammatory Pericardial Effusion
|
Pericardium Effusion
|
|
|
| Ankylosing Spondylitis 1 |
|
Ankylosing Spondylitis, Susceptibility To, 1
|
|
|
| Limb Ischemia |
|
|
| Critical Illness Polyneuropathy |
|
Polyneuropathy, Critical Illness
|
|
|
| Vertebral Artery Occlusion |
|
Occlusion And Stenosis Of Vertebral Artery
|
|
|
| Mediastinitis |
|
|
| Acalculous Cholecystitis |
|
Acute Cholecystitis Without Calculus
|
Acute Acalculous Cholecystitis
|
|
Cholecystitis Without Calculus
|
|
|
| Tricuspid Valve Insufficiency |
|
Tricuspid Regurgitation
|
Tricuspid Valve Regurgitation
|
|
Tricuspid Incompetence
|
Tr - [Tricuspid Regurgitation]
|
|
Tricuspid Valve Incompetency
|
Tricuspid Valve Annular Incompetency
|
|
|
| Middle Cerebral Artery Infarction |
|
Infarction, Middle Cerebral Artery
|
Infarction Middle Cerebral Artery
|
|
|
| Angiodysplasia |
|
Angiodysplasia Of Colon
|
Angiodysplasia Of Stomach And Duodenum With Hemorrhage
|
|
Angiodysplasia Of Large Intestine
|
Telangiectasia Of Colon
|
|
Vascular Ectasia Of Colon
|
Av - [Angiodysplasia Malformation Of Colon]
|
|
Colon Angiodysplasia
|
Colonic Angiodysplasia
|
|
Vascular Ectasia Of Large Intestine
|
|
|
| Mastoiditis |
|
|
| Rocky Mountain Spotted Fever |
|
Brazillian Spotted
|
Choix
|
|
Exanthematic Typhus Of Sao Paulo
|
Fiebre Maculosa
|
|
Fiebre Manchada
|
Sao Paulo Typhus
|
|
So Paulo Fever
|
Tick Typhus
|
|
Tobia Fever
|
Rmsf
|
|
Typhus, Tick
|
|
|
| Cholesterol Embolism |
|
Atheroembolism
|
Trash Foot
|
|
Cholesterol Crystal Embolism
|
Purple Toe Syndrome
|
|
Warfarin Blue Toe Syndrome
|
Embolism, Cholesterol
|
|
Cholesterol Embolus Syndrome
|
|
|
| Mitral Valve Stenosis |
|
Mitral Stenosis
|
Rheumatic Mitral Stenosis
|
|
Ms - [Mitral Stenosis]
|
Mitral Valvular Stricture
|
|
Mitral Valve Stricture
|
Mitral Stricture
|
|
Chronic Mitral Stenosis
|
Mitral Obstruction
|
|
Mitral Valve Obstruction
|
Mitral Stenosis With Incompetence
|
|
Mitral Stenosis With Regurgitation
|
Rheumatic Mitral Insufficiency With Obstruction
|
|
|
| Astrakhan Spotted Fever |
|
|
| Tricuspid Valve Stenosis |
|
Tricuspid Stenosis
|
Tricuspid Stricture
|
|
Tricuspid Valve Stricture
|
Tricuspid Insufficiency With Obstruction
|
|
Tricuspid Insufficiency With Stenosis
|
|
|
| Basilar Artery Occlusion |
|
|
| Acquired Thrombocytopenia |
|
Secondary Thrombocytopenia
|
|
|
| Viral Pneumonia |
|
Pneumonia, Viral
|
Acute Viral Pneumonia
|
|
Bronchopneumonia Due To Viruses Other Than Influenza Viruses
|
Interstitial Viral Pneumonia
|
|
Viral Bronchopneumonia
|
Viral Double Pneumonia
|
|
Viral Lobar Pneumonia
|
Viral Purulent Pneumonia
|
|
Virus Interstitial Pneumonia
|
Virus Lobar Pneumonia
|
|
|
| Cecal Disease |
|
Cecal Diseases
|
Disorder Of Cecum
|
|
|
| Mitral Valve Disease |
|
Chronic Rheumatic Mitral Valve
|
Rheumatic Mitral Insufficiency
|
|
Disease Of Mitral Valve
|
Mitral Rh Valve Dis.
|
|
Rheumatic Disease Of Mitral Valve
|
Rheumatic Mitral Valve Changes
|
|
Rheumatic Mitral Valve Incompetence
|
Rheumatic Mitral Valve Regurgitation
|
|
Abnormality Of The Mitral Valve
|
Diseases Of Mitral Valve
|
|
Rheumatic Mitral Regurgitation
|
|
|
| Livedoid Vasculitis |
|
Livedoid Vasculopathy
|
Livedo Reticularis With Summer Ulcerations
|
|
Livedo Vasculitis
|
Livedo Reticularis With Winter Ulcerations
|
|
Segmental Hyalinizing Vasculopathy
|
Milian Atrophie Blanche
|
|
Segmental Hyalinizing Vasculitis
|
Livedo Reticularis With Summer Ulceration
|
|
|
| Aspiration Pneumonitis |
|
Chemical Pneumonitis
|
Mendelson'S Syndrome
|
|
Aspiration Pneumonia
|
Pneumonitis Due To Fumes And/Or Vapors
|
|
Toxic Pneumonitis
|
Mendelson'S Syndrome Resulting From A Procedure
|
|
Mendelson Syndrome Resulting From A Procedure
|
Pulmonary Acid Aspiration Syndrome
|
|
Pneumonitis Due To Inhalation Of Gastric Secretions
|
Mendelson Syndrome Due To Anaesthesia During Labour And Delivery
|
|
Inhalation Of Stomach Contents Or Secretions, Nos Due To Anaesthesia During Labour And Delivery
|
|
|
| Aspiration Pneumonia |
|
Pneumonia, Aspiration
|
Pneumonia Aspiration
|
|
Aspiration Pneumonitis
|
|
|
| Aortic Valve Insufficiency |
|
Aortic Regurgitation
|
Rheumatic Aortic Regurgitation
|
|
Aortic Insufficiency
|
Rheumatic Aortic Insufficiency
|
|
Rheumatic Aortic Valve Insufficiency
|
Aortic Incompetence
|
|
Corrigan'S Disease
|
Rheumatic Aortic Valve Regurgitation
|
|
Aortic Valve Incompetency
|
Ai - [Aortic Incompetence]
|
|
Incompetent Aortic Valve
|
Ar - [Aortic Regurgitation]
|
|
Calcific Aortic Valve Regurgitation
|
Myxomatous Aortic Valve Regurgitation
|
|
Annular Incompetency Of Aortic Valve
|
Austin Flint Murmur
|
|
Flint Murmur
|
Rheumatic Aortic Incompetence
|
|
Rheumatic Ai - [Aortic Insufficiency]
|
|
|
| Hypothyroidism |
|
Thyroid Diseases
|
Thyroid Disease
|
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
|
Dysfunction Thyroid
|
Thyroid Dysfunction
|
|
|
| Thrombocytopenic Purpura, Autoimmune |
|
Idiopathic Thrombocytopenic Purpura
|
Autoimmune Thrombocytopenic Purpura
|
|
Immune Thrombocytopenic Purpura
|
Itp
|
|
Idiopathic Purpura
|
AITP
|
|
Ideopath Thrombocytopenic Pur
|
Primary Thrombocytopenic Purpura
|
|
Werlhof'S Disease
|
Thrombocytopenic Purpura Autoimmune
|
|
Purpura Thrombocytopenic Idiopathic
|
Purpura, Thrombocytopenic, Idiopathic
|
|
Autoimmune Thrombocytopenia
|
Thrombocytopenia Due To Platelet Alloimmunization
|
|
Idiopathic Thrombocytopenia
|
Idiopathic Thrombocytopenia Purpura
|
|
Frank'S Essential Thrombocytopenia
|
Itp - [Idiopathic Thrombocytopenia Purpura]
|
|
Werlhof Disease
|
Primary Autoimmune Thrombocytopenic Purpura
|
|
Haemorrhagic Purpura
|
Essential Thrombocytopenia
|
|
Purpura Haemorrhagica
|
|
|
| Critical Covid-19 |
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| Thrombocytopenia Due To Platelet Alloimmunization |
|
Immune Thrombocytopenia
|
Autoimmune Thrombocytopenia
|
|
Immune Thrombocytopenic Purpura
|
Itp
|
|
Auto-Immune Thrombocytopenia
|
Thrombocytopenia Due To Immune Destruction
|
|
Autoimmune Thrombocytopenic Purpura
|
Idiopathic Thrombocytopenic Purpura
|
|
Werlhof Disease
|
|
|
| Central Retinal Vein Occlusion |
|
|
| Marburg Hemorrhagic Fever |
|
Marburg Virus Disease
|
Marburg Disease
|
|
Green Monkey Disease
|
Mhf
|
|
Vervet Monkey Disease
|
Mard - [Marburg Disease]
|
|
Mvd - [Marburg Virus Disease]
|
Marburg Haemorrhagic Fever
|
|
Mhf - [Marburg Haemorrhagic Fever]
|
|
|
| Volvulus Of Midgut |
|
Volvulus
|
Intestinal Volvulus
|
|
Intestinal Malrotation, Familial
|
Familial Intestinal Malrotation
|
|
Twist Of Intestine, Bowel, Or Colon
|
|
|
| Necrotizing Fasciitis |
|
|
| Transient Cerebral Ischemia |
|
Transient Ischemic Attack
|
Transient Ischemic Attacks
|
|
Tia
|
Tia - Transient Ischaemic Attack
|
|
Transient Cerebral Ischaemia
|
Ischemic Attack, Transient
|
|
Intermittent Cerebral Ischemia
|
Tia - [Transient Ischaemic Attack]
|
|
Intermittent Cerebral Ischaemia
|
Transient Cerebral Ischaemic Attack, Unspecified, Course Of Resolution Unspecified
|
|
|
| Severe Pre-Eclampsia |
|
Severe Preeclampsia
|
Antepartum Severe Pre-Eclampsia
|
|
Postpartum Severe Pre-Eclampsia
|
Severe Pre-Eclampsia, With Delivery
|
|
Severe Toxemia
|
Severe Pre-Eclampsia, Antepartum Condition Or Complication
|
|
Severe Pre-Eclampsia, Postpartum Condition Or Complication
|
Severe Puerperal Pre-Eclampsia
|
|
Severe Pre-Eclamptic Toxaemia
|
Severe Pet - [Pre-Eclamptic Toxaemia]
|
|
|
| Hypersplenism |
|
Hypersplenia
|
Big Spleen Syndrome
|
|
Hyperfunction Of Spleen
|
Increased Splenic Activity
|
|
Spleen Metaplasia
|
Splenic Metaplasia
|
|
|
| Kidney Cortex Necrosis |
|
|
| Nephrotic Syndrome |
|
Finnish Congenital Nephrotic Syndrome
|
Ns - [Nephrotic Syndrome]
|
|
Nephrosis Syndrome
|
Nephrosis Nos
|
|
Glomerular Lesion Nephrosis
|
|
|
| Medulloadrenal Hyperfunction |
|
|
| Acquired Polycythemia |
|
Secondary Polycythemia
|
Polycythemia, Secondary
|
|
Secondary Erythrocytosis
|
Polycythemia Secondary
|
|
|
| Peptic Ulcer Disease |
|
Peptic Ulcer
|
Acute Peptic Ulcer With Hemorrhage
|
|
Acute Peptic Ulcer With Hemorrhage And Perforation
|
Acute Peptic Ulcer Without Hemorrhage And Without Perforation
|
|
|
| Splenic Disease |
|
Splenic Diseases
|
Dyssplenism
|
|
Spleen Disease
|
Abnormality Of The Spleen
|
|
Spleen Diseases
|
|
|
| Pericoronitis |
|
|
| Mitral Valve Insufficiency |
|
Mitral Regurgitation
|
Congenital Insufficiency Of Mitral Valve
|
|
Congenital Mitral Insufficiency
|
Congenital Mitral Regurgitation
|
|
Mitral Valve Incompetence
|
Mitral Valve Regurgitation
|
|
Mr - [Mitral Regurgitation]
|
Mi - [Mitral Incompetence]
|
|
Mitral Valve Annular Incompetency
|
Congenital Mitral Valve Incompetence
|
|
Congenital Mitral Valve Insufficiency
|
Congenital Mitral Valve Regurgitation
|
|
Congenital Mitral Incompetence
|
|
|
| Dic In Newborn |
|
Disseminated Intravascular Coagulation In Newborn
|
|
|
| Ischemic Colitis |
|
Colitis, Ischemic
|
Irreversible Ischaemic Colitis
|
|
|
| Exanthem |
|
|
| Heart Aneurysm |
|
|
| Retinal Vascular Occlusion |
|
Retinal Vasc. Occlusion
|
Occlusion Of Retinal Vessels
|
|
Retinal Obstruction
|
|
|
| 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
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Cellulitis |
|
|
| Blood Protein Disease |
|
Blood Protein Disorders
|
Blood Protein Disorder
|
|
|
| Coronary Aneurysm |
|
Aneurysm Of Coronary Vessels
|
Aneurysmal Lesion Of Coronary Artery
|
|
Arteriovenous Aneurysm Of Coronary Vessels
|
|
|
| Autoimmune Disease |
|
Autoimmune Diseases
|
Autoimmune Hypersensitivity Disease
|
|
Hypersensitivity Reaction Type Ii Disease
|
Type Ii Hypersensitivity Reaction Disease
|
|
|
| Horner'S Syndrome |
|
Horner Syndrome
|
Bernard-Horner Syndrome
|
|
Oculosympathetic Palsy
|
Bernard Horner Syndrome
|
|
Cervical Sympathetic Paralysis
|
Von Passow Syndrome
|
|
Cervical Sympathetic Dystrophy
|
|
|
| Cavernous Hemangioma |
|
Hemangioma, Cavernous
|
Cavernoma
|
|
Cavernous Haemangioma
|
|
|
| Paralytic Ileus |
|
Adynamic Ileus
|
Paralytic Ileus Of Bowel
|
|
Ileus Nos
|
Paralysis Of Bowel
|
|
Paralysis Of Intestine
|
Adynamic Intestinal Obstruction
|
|
Paralytic Intestinal Ileus
|
|
|
| Hemorrhoid |
|
Hemorrhoids
|
Hemorrhoidal Disease
|
|
Rectal Diseases
|
Piles
|
|
Unspecified Haemorrhoids Without Complication
|
|
|
| Arteriovenous Malformation |
|
Arteriovenous Malformations
|
Arteriovenous Hemangioma
|
|
Cirsoid Aneurysm
|
Racemose Aneurysm
|
|
Racemose Angioma
|
Racemose Hemangioma
|
|
Congenital Arteriovenous Malformation
|
|
|
| Spotted Fever |
|
Spotted Fevers
|
Spotted Fever Group Rickettsial Disease
|
|
Tick-Borne Rickettsioses
|
Tick-Borne Typhus Nos
|
|
Rocky Mountain Spotted Fever
|
Sao Paulo Fever
|
|
Sao Paulo Typhus
|
Lone Star Spotted Fever
|
|
Colombian Spotted Fever
|
American Spotted Fever
|
|
Tick Typhus Due To Rickettsia Rickettsii
|
Rocky Mountain Tick Fever
|
|
Boutonneuse Fever
|
Mediterranean Tick Fever
|
|
Fièvre Boutonneuse
|
Mediterranean Spotted Fever
|
|
Tick Typhus Due To Rickettsia Conorii
|
African Tick Typhus
|
|
Indian Tick Typhus
|
Kenya Tick Typhus
|
|
North Asian Tick Fever
|
Siberian Tick Typhus
|
|
Tick Typhus Due To Rickettsia Siberica
|
North Asian Spotted Fever
|
|
Queensland Tick Typhus
|
Queensland Fever
|
|
|
| Analbuminemia |
|
ANALBA
|
Congenital Analbuminemia
|
|
Hypoalbuminemia
|
|
|
| Coronary Artery Vasospasm |
|
Coronary Vasospasm
|
Coronary Artery Spasm
|
|
|
| Vulvar Angiokeratoma |
|
Fordyce Angiokeratoma Of Vulva
|
Angiokeratoma Of Vulva
|
|
|
| Kidney Papillary Necrosis |
|
Necrotizing Renal Papillitis
|
Papillary Necrosis
|
|
Renal Papillitis Necrotizing
|
|
|
| Dengue Hemorrhagic Fever |
|
Severe Dengue
|
Dengue Haemorrhagic Fever
|
|
Dhf
|
Severe Dengue Haemorrhagic Fever
|
|
Severe Dengue Fever
|
Dengue Shock Syndrome
|
|
|
| Heart Valve Disease |
|
Heart Valve Diseases
|
Valvular Heart Disease
|
|
Valvular Heart Diseases
|
Heart Valve Prolapse
|
|
|
| Atrial Heart Septal Defect |
|
Atrial Septal Defect
|
Atrial Septal Defects
|
|
Atrioseptal Defect
|
Auricular Septal Defect
|
|
Congenital Atrial Septal Defect
|
Interatrial Septal Defect
|
|
Interauricular Septal Defect
|
Heart Septal Defects, Atrial
|
|
Septal Defect, Atrial
|
|
|
| Cauda Equina Syndrome |
|
Cauda Equina
|
Polyradiculopathy
|
|
|
| Bilirubin Metabolic Disorder |
|
Hyperbilirubinemia
|
Hereditary Hyperbilirubinemia
|
|
Hyperbilirubinemia, Hereditary
|
Hyperbilirubinaemia
|
|
|
| Klebsiella Pneumonia |
|
Pneumonia Due To Klebsiella Pneumoniae
|
Klebsiella Infections
|
|
Doid:13272
|
Klebsiella Lobar Pneumonia
|
|
|
| Hypertension, Essential |
|
Essential Hypertension
|
Hypertension
|
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
|
Hypertensive Disease
|
Primary Hypertension
|
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
|
Hyperpiesia
|
Idiopathic Hypertension
|
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
|
Htn
|
Vascular Hypertensive Disorder
|
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
|
Arterial Hypertension Nos
|
Hypertension Nos
|
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
|
Systemic Hypertension
|
Artery Htn
|
|
Benign Htn
|
Vascular Htn
|
|
Vascular Hypertension
|
Cholesterol Hypertension
|
|
Cholesterol Htn
|
Idiopathic Htn
|
|
Malignant Hypertension
|
Malignant Htn
|
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
|
Hypertensive Vascular Degeneration
|
|
|
| Aortic Dissection |
|
|
| 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
|
|
|
| Renal Pelvis Squamous Cell Carcinoma |
|
Epidermoid Carcinoma Of The Kidney Pelvis
|
Squamous Cell Carcinoma Of Renal Pelvis
|
|
|
| Gastric Hemangioma |
|
|
| Respiratory Failure |
|
Acute Respiratory Failure
|
Chronic Respiratory Failure
|
|
Respiratory Insufficiency
|
Acute-On-Chronic Respiratory Failure
|
|
Respiratory Disease
|
Acute And Chronic Respiratory Failure
|
|
Respiratory Insufficiency/Failure
|
Chronic Respiratory Disease
|
|
Pulmonary Valve Insufficiency
|
Chronic Disease Of Respiratory System
|
|
Respiration Disorders
|
Respiratory Tract Diseases
|
|
Lung Failure Nos
|
Pulmonary Failure
|
|
Arf - [Acute Respiratory Failure]
|
Acute Respiratory Insufficiency
|
|
Acute Pulmonary Insufficiency
|
Acute Respiration Failure
|
|
Chronic Respiration Failure
|
|
|
| Extrinsic Cardiomyopathy |
|
|
| Pleural Disease |
|
Pleural Diseases
|
Disorder Of Pleura
|
|
Non-Neoplastic Pleural Disease
|
Pleural Disorders
|
|
Non-Neoplastic Pleural Disorder
|
|
|
| Type 2 Diabetes Mellitus |
|
Insulin Resistance
|
NIDDM
|
|
Type 2 Diabetes
|
Diabetes Mellitus, Non-Insulin-Dependent
|
|
T2D
|
Noninsulin-Dependent Diabetes Mellitus
|
|
Diabetes Mellitus, Type Ii
|
Maturity-Onset Diabetes
|
|
Insulin Resistance, Severe, Digenic
|
Diabetes Mellitus, Type 2
|
|
Diabetes Mellitus, Noninsulin-Dependent
|
Diabetes Mellitus, Noninsulin-Dependent, Association With
|
|
Diabetes Mellitus, Noninsulin-Dependent, Late Onset
|
Hypertension, Insulin Resistance-Related, Susceptibility To
|
|
Insulin Resistance, Susceptibility To
|
Non-Insulin-Dependent Diabetes Mellitus
|
|
Type Ii Diabetes Mellitus
|
Adult-Onset Diabetes Mellitus
|
|
Maturity-Onset Diabetes Mellitus
|
Diabetes Mellitus Type 2
|
|
Type Ii Diabetes
|
Type 2 Diabetes Mellitus, Susceptibility To
|
|
Diabetes, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To
|
|
Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 2, Susceptibility To
|
|
Diabetes Mellitus, Noninsulin-Dependent, 2
|
Diabetes Mellitus, Type Ii, Susceptibility To
|
|
Hypertension, Insulin Resistance-Related
|
Adult-Onset Diabetes
|
|
Aodm
|
Diabetes Mellitus, Adult-Onset
|
|
Diabetes Mellitus Type Ii
|
Diabetes Mellitus Type 2, Susceptibility To
|
|
Diabetes, Type Ii, Susceptibility To
|
Diabetes Type 2
|
|
Diabetes Mellitus
|
Adult Onset Diabetes
|
|
Maturity Onset Diabetes
|
Nonketotic Diabetes
|
|
Non-Insulin Dependent Diabetes Mellitus
|
T2dm - [Type 2 Diabetes Mellitus]
|
|
Niddm - [Non Insulin Dependent Diabetes Mellitus]
|
Dm2
|
|
Dm Type Ii
|
Diabetic Type 2
|
|
Insulin Requiring Type 2 Diabetes
|
Noninsulin Dependent Diabetes
|
|
Non-Insulin-Dependent Diabetes Mellitus Without Complications
|
Diabetes Due To Insulin Secretory Defect
|
|
Diabetes Mellitus Due To Insulin Secretory Defect
|
Non-Insulin-Dependent Diabetes Of The Young
|
|
Senile Diabetes
|
Nonketotic Hyperglycaemia
|
|
Stable Diabetes
|
|
|
| Hemolytic Uremic Syndrome, Atypical 1 |
|
Atypical Hemolytic-Uremic Syndrome
|
Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1
|
|
Atypical Hemolytic Uremic Syndrome
|
Hemolytic Uremic Syndrome, Atypical, Susceptibility To
|
|
Ahus
|
AHUS1
|
|
Hemolytic-Uremic Syndrome
|
Ahus 1
|
|
Ahus, Susceptibility To, 1
|
Hemolytic Uremic Syndrome, Atypical
|
|
Non-Shiga-Like Toxin-Associated Hus
|
Non-Stx-Hus
|
|
Nonenteropathic Hus
|
Atypical Hus
|
|
Shiga Toxin-Associated Hemolytic Uremic Syndrome
|
D+ Hus
|
|
Ehec-Hus
|
Hemolytic Uremic Syndrome Associated With Shiga Toxin-Producing Escherichia Coli
|
|
Hemolytic Uremic Syndrome With Diarrhea
|
Stec-Hus
|
|
Shiga-Like Toxin-Associated Hus
|
Stx-Hus
|
|
Typical Hus
|
Typical Hemolytic Uremic Syndrome
|
|
Atypical Hemolytic Uremic Syndrome With Anti-Factor H Antibodies
|
Atypical Hus With Anti-Factor H Antibodies
|
|
Ahus With Anti-Factor H Antibodies
|
Ahus With Neutralizing Autoantibodies Against Factor H
|
|
Hemolytic Uremic Syndrome Atypical 1
|
Atypical Hemolytic Uremic Syndrome With H Factor Anomaly
|
|
D Hus
|
Hemolytic-Uremic Syndrome Without Diarrhea
|
|
Hemolytic-Uremic Syndrome, Atypical, Type 1
|
Hemolytic Uremic Syndrome, Typical
|
|
|
| Urinary Tract Infection |
|
Urinary Tract Infections
|
Uti
|
|
Urinary Tract Infection Nos
|
Uti - [Urinary Tract Infection]
|
|
Uti Nos - [Urinary Tract Infection Nos]
|
Urosepsis Nos
|
|
E Coli Uti
|
E Coli Urinary Tract Infection
|
|
Escherichia Coli Uti
|
|
|
| Hemophagocytic Lymphohistiocytosis |
|
Lymphohistiocytosis, Hemophagocytic
|
Haemophagocytic Syndrome
|
|
Lymphohistiocytosis Hemophagocytic
|
Hemophagocytic Syndrome
|
|
Familial Hemophagocytic Lymphocytosis
|
Histiocytoses Of Mononuclear Phagocytes
|
|
Haemophagocytic Lymphohistiocytosis Nos
|
|
|
| Sickle Cell Anemia |
|
Hemoglobin Sc Disease
|
Anemia, Sickle Cell
|
|
Hbsc Disease
|
Sickle Cell-Hemoglobin C Disease Syndrome
|
|
Hb Ss Disease
|
Sickle Cell Trait
|
|
Drepanocytosis
|
Haemoglobin Sc Disease
|
|
Hb Sc Disease
|
Hb-S/Hb-C Disease
|
|
Hb-Ss Disease Without Crisis
|
Hemoglobin S Disease Without Crisis
|
|
Sickle Cell Anaemia
|
Sickle-Cell/Hb-C Disease Without Crisis
|
|
Sickle Cell - Hemoglobin C Disease
|
Hbs Disease
|
|
Hemoglobin S Disease
|
Sickling Disorder Due To Hemoglobin S
|
|
SKCA
|
Sickle Cell Disease
|
|
Sickle Cell-Hemoglobin C Disease
|
Sickle-Cell Disease Carrier
|
|
Sickle-Cell Heterozygous Disorder
|
Haemoglobin A-S Genotype
|
|
Hb-S - [Sickle Cell Haemoglobin] Carrier
|
Sickle Cell Haemoglobin Trait
|
|
As - [Sickle Cell Trait]
|
Hbas - [Sickle Cell Haemoglobin Trait]
|
|
Sickle-Cell Trait Haemoglobin Disease
|
Haemoglobin Sickle Cell Trait Disorder
|
|
Heterozygous Sickle Cell Trait
|
Hbas - [Heterozygous Haemoglobin S]
|
|
|
| Diabetes Mellitus |
|
|
| Acute Hemorrhagic Encephalitis |
|
|
| Heart Septal Defect |
|
Septal Defect
|
Heart Septal Defects
|
|
Cardiac Septal Defects
|
Congenital Septal Defect Of Heart
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Moyamoya Disease 1 |
|
Moyamoya Disease
|
Spontaneous Occlusion Of The Circle Of Willis
|
|
Mymy
|
Progressive Intracranial Arterial Occlusion
|
|
Moyamoya Syndrome
|
MYMY1
|
|
Cerebrovascular Moyamoya Disease
|
Moya-Moya Disease
|
|
Progressive Intracranial Occlusive Arteropathy
|
Idiopathic Moyamoya Disease
|
|
|
| Intracranial Berry Aneurysm |
|
Familial Aneurysmal Subarachnoid Hemorrhage
|
Familial Berry Aneurysm
|
|
Familial Intracranial Saccular Aneurysm
|
Saccular Cerebral Aneurysm
|
|
Aneurysm, Intracranial Berry
|
Aneurysmal Subarachnoid Hemorrhage
|
|
Aneurysm, Intracranial Berry, 1
|
|
|
| Osteoporosis |
|
Postmenopausal Osteoporosis
|
Osteoporosis, Postmenopausal
|
|
Bone Mineral Density Quantitative Trait Locus
|
Bmnd
|
|
Osteoporosis, Involutional
|
Osteoporosis, Susceptibility To
|
|
Osteoporosis, Postmenopausal, Susceptibility
|
Bone Mineral Density Variation Qtl, Osteoporosis
|
|
OSTEOP
|
Involutional Osteoporosis
|
|
Senile Osteoporosis
|
Osteoporosis Postmenopausal
|
|
Bone Mineral Density, Quantitative Trait Locus
|
Osteoporosis, Senile
|
|
Idiopathic Osteoporosis
|
Bone Rarefaction Nos
|
|
Type 1 Osteoporosis
|
|
|
| Heart Disease |
|
Heart Failure
|
Congenital Heart Disease
|
|
Heart Diseases
|
Congenital Heart Defects
|
|
Congenital Heart Defect
|
Heart Malformation
|
|
Congenital Anomaly Of Heart
|
Heart Defect
|
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
|
Heart Defects
|
Heart Disease, Congenital
|
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
| Inguinal Hernia |
|
Hernia Inguinal
|
Hernia, Inguinal
|
|
Inguinal Hernias
|
Bubonocele
|
|
Indirect Inguinal Hernia
|
Direct Inguinal Hernia
|
|
Oblique Inguinal Hernia
|
Scrotal Hernia
|
|
Ih - [Inguinal Hernia]
|
|
|
| Aortic Aneurysm, Familial Abdominal, 1 |
|
Abdominal Aortic Aneurysm
|
Aortic Aneurysm, Familial Abdominal 1
|
|
Aneurysm, Abdominal Aortic
|
AAA
|
|
Aortic Aneurysm, Abdominal
|
AAA1
|
|
Aortic Aneurysm, Familial Abdominal
|
Aortic Aneurysm Abdominal
|
|
Abdominal Aortic Aneurysms
|
Abdominal Aortic Aneurysm Without Mention Of Perforation Or Rupture
|
|
Abdomen Aneurysm
|
Abdominal Aorta Aneurysm
|
|
Aneurysm Of Abdominal Aorta
|
Aortic Abdomen Aneurysm
|
|
Aaa - [Abdominal Aortic Aneurysm]
|
Abdominal Aneurysm
|
|
Abdominal Aorta Aneurysm Rupture
|
Abdominal Aorta Aneurysm Ruptured
|
|
Abdominal Aortic Aneurysm Which Has Ruptured
|
Ruptured Aaa
|
|
Abdomen Aorta Aneurysm Ruptured
|
Abdomen Aorta Rupture
|
|
Abdomen Aortic Aneurysm Rupture
|
Abdomen Aneurysm Rupture
|
|
Abdomen Aortic Aneurysm Ruptured
|
Abdomen Aortic Rupture
|
|
Abdominal Aorta Rupture
|
Abdominal Aortic Rupture
|
|
Rupture Abdomen Aorta Aneurysm
|
Rupture Abdominal Aortic Aneurysm
|
|
Ruptured Abdomen Aneurysm
|
Ruptured Abdomen Aorta
|
|
Ruptured Abdomen Aortic
|
Ruptured Abdominal Aneurysm
|
|
Ruptured Abdominal Aorta
|
Ruptured Abdominal Aortic
|
|
Ruptured Aorta Abdominalis Aneurysm
|
False Abdomen Aorta Aneurysm Ruptured
|
|
False Abdominal Aortic Aneurysm Ruptured
|
False Abdominal Aorta Aneurysm Ruptured
|
|
False Abdomen Aortic Aneurysm Ruptured
|
|
|
| Patent Ductus Arteriosus 1 |
|
Patent Ductus Arteriosus
|
PDA1
|
|
Pda
|
Ductus Arteriosus, Patent
|
|
Patent Ductus Arteriosus, Susceptibility To
|
Patent Ductus Botalli
|
|
Patency Of The Ductus Arteriosus
|
Patent Ductus Arteriosus Familial
|
|
Ductus Arteriosus Patent
|
Patent Ductus Arteriosus - Persisting Type
|
|
|
| Behcet Syndrome |
|
Behcet Disease
|
Behcet'S Syndrome
|
|
Behcet'S Disease
|
Behçet Disease
|
|
Bd
|
Adamantiades-Behcet Disease
|
|
Triple Symptom Complex
|
Behçet'S Disease
|
|
Behet'S Syndrome
|
Bd Syndrome
|
|
Behçet Syndrome
|
Behçet'S Syndrome
|
|
Behcet Triple Symptom Complex
|
Malignant Aphthosis
|
|
Old Silk Route Disease
|
Adamantiades-Behçet Disease
|
|
|
| Migraine With Or Without Aura 1 |
|
Migraine
|
Migraine With Or Without Aura, Susceptibility To, 1
|
|
Migraine Disorder
|
Migraine Variant
|
|
Migraines
|
Migraine Disorders
|
|
Mgr1
|
Mgau
|
|
Ma
|
Migraine With Or Without Aura
|
|
Classic Migraine
|
Common Migraine
|
|
Disorder, Migraine
|
Headache Migraine
|
|
Headache Migrainous
|
Migraine Headache
|
|
Migraine Syndrome
|
Headache Including Migraine
|
|
Migraine, Susceptibility To
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Peripheral Nervous System Disease |
|
Peripheral Neuropathy
|
Peripheral Nerve Disease
|
|
Peripheral Nerve Disorders
|
Neuropathy, Peripheral
|
|
Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
|
|
|
