| Diseases |
Alias |
|
| 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
|
|
|
| Von Willebrand Disease, Type 2 |
|
Von Willebrand Disease Type 2m
|
Von Willebrand Disease Type 2
|
|
Von Willebrand Disease Type 2a
|
Von Willebrand Disease Type 2b
|
|
Von Willebrand Disease Type 2n
|
VWD2
|
|
Von Willebrand'S Disease 2
|
Von Willebrand Disease Type Ii
|
|
Von Willebrand Disease, Type Ii
|
Vwd, Type 2
|
|
Von Willebrand Disease, Types 2a, 2b, 2m, And 2n
|
Vwd Type 2
|
|
Von Willebrand Disease 2
|
Von Willebrand Disease Normandy Variant
|
|
Von Willebrand Disease Type 2 Malmo
|
Von Willebrand Disease Type I New York
|
|
Von Willebrand Factor Deficiency Type 2
|
Vwd2a
|
|
Vwd2b
|
Vwd2m
|
|
Vwd2n
|
Von Willebrand Disease, Type 2a, 2b, 2m, And 2n
|
|
Von Willebrand Disease, Type 2a
|
Von Willebrand Disease, Type 2b
|
|
Von Willebrand Disease, Type 2n
|
|
|
| Von Willebrand Disease, Type 3 |
|
Von Willebrand Disease Type 3
|
VWD3
|
|
Von Willebrand'S Disease 3
|
Von Willebrand Disease Type Iii
|
|
Von Willebrand Disease, Type Iii
|
Vwd, Type 3
|
|
Vwd Type 3
|
Von Willebrand Disease 3
|
|
Von Willebrand Disease Recessive Form
|
Von Willebrand Factor Deficiency Type 3
|
|
|
| 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
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| 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
|
|
|
| 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
|
|
|
| Peripheral Vascular Disease |
|
Peripheral Arterial Disease
|
Arterial Occlusive Disease
|
|
Arterial Occlusive Diseases
|
Pad
|
|
Peripheral Vascular Diseases
|
Peripheral Occlusive Disease
|
|
Peripheral Arterial Diseases
|
Helicobacter Infections
|
|
|
| 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
|
|
|
| Intermittent Claudication |
|
Charcot'S Syndrome
|
Amyotrophic Lateral Sclerosis
|
|
|
| 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
|
|
|
| Pseudo-Von Willebrand Disease |
|
Bdplt3
|
Von Willebrand Disease, Platelet-Type
|
|
VWDP
|
Platelet-Type Bleeding Disorder 3
|
|
Platelet Type-Von Willebrand Disease
|
Pt-Vwd
|
|
Von Willebrand Disease Platelet-Type
|
Von Willebrand Disease, Platelet Type
|
|
Pseudo Von Willebrand Disease
|
Bleeding Disorder, Platelet-Type, 3
|
|
Pseudo-Von Willebrand Disease Type 2b
|
Bleeding Disorder Platelet-Type 3
|
|
Pseudo-Vwd
|
|
|
| Blood Platelet Disease |
|
Platelet Disorder
|
Blood Platelet Disorders
|
|
Thrombocytopathy
|
Platelet Dysfunction
|
|
Platelet Disorders
|
Qualitative Platelet Deficiency
|
|
|
| Hypertensive Retinopathy |
|
|
| 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
|
|
|
| Hemophilia |
|
Haemophilia
|
Hemophilia, Familial
|
|
Hemophilia, Hereditary
|
Hemophilia A
|
|
Hemophilia, 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
|
|
|
| Acquired Von Willebrand Syndrome |
|
Acquired Von Willebrand Disease
|
Willebrand Disease, Acquired
|
|
Avws
|
|
|
| Eisenmenger Syndrome |
|
|
| 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 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
|
|
|
| Afibrinogenemia, Congenital |
|
Congenital Afibrinogenemia
|
Afibrinogenemia
|
|
Factor I Deficiency
|
Familial Afibrinogenemia
|
|
Hypofibrinogenemia, Congenital
|
Fibrinogen Deficiency
|
|
Afibrinogenemia Congenital
|
CAFBN
|
|
Congenital Hypofibrinogenemia
|
Hypofibrinogenemia
|
|
Complement Factor I Deficiency
|
|
|
| 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
|
|
|
| Venous Insufficiency |
|
Peripheral Venous Insufficiency
|
|
|
| Uremia |
|
|
| 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]
|
|
|
| Thrombophilia |
|
|
| 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
|
|
|
| Thrombosis |
|
Thrombosis Of Blood Vessel
|
|
|
| Purpura |
|
|
| Platelet Aggregation, Spontaneous |
|
|
| Malignant Hypertension |
|
Hypertension, Malignant
|
Hypertension Malignant
|
|
|
| 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
|
|
|
| Gray Platelet Syndrome |
|
Platelet Alpha-Granule Deficiency
|
GPS
|
|
Bdplt4
|
Bleeding Disorder, Platelet-Type, 4
|
|
Grey Platelet Syndrome
|
Platelet-Type Bleeding Disorder 4
|
|
Marked Decrease Or Absence Of Alpha-Granules And Of Platelet-Specific Alpha-Granule Proteins
|
Deficient Alpha Granule Syndrome
|
|
Platelet Alpha Granule Deficiency
|
Platelet Granule Defect
|
|
Alpha Storage Pool Deficiency
|
Bleeding Disorder Platelet-Type 4
|
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
| Essential Thrombocythemia |
|
Essential Thrombocytosis
|
Familial Thrombocytosis
|
|
Hemorrhagic Thrombocythemia
|
Hereditary Thrombocythemia
|
|
Primary Thrombocytosis
|
Idiopathic Thrombocythemia
|
|
Primary Thrombocythemia
|
Thrombocythemia, Essential
|
|
Essential Thrombocythaemia
|
Et
|
|
Familial Thrombocythemia
|
Thrombocythemia Essential
|
|
|
| Vasculitis |
|
Angiitis
|
Autoimmune Vasculitis
|
|
Systemic Vasculitis
|
Vasculitis, Autoimmune
|
|
|
| Intracranial Thrombosis |
|
Cerebral Thrombosis
|
Thrombosis Of Cerebral Veins
|
|
Cerebral Arterial Thrombosis
|
|
|
| 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
|
|
|
| Coronary Thrombosis |
|
Coronary Artery Thrombosis
|
|
|
| Carotid Stenosis |
|
Carotid Artery Stenosis
|
Stenosis, Carotid Artery
|
|
|
| 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
|
|
|
| Varicose Veins |
|
Varices
|
Varix
|
|
Venous Ectasia
|
Venous Varices
|
|
Varicosity
|
|
|
| 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
|
|
|
| Pulmonary Embolism |
|
Pulmonary Artery Embolism
|
Pulmonary Embolus
|
|
Pulmonary Emboli
|
|
|
| Raynaud Disease |
|
Raynaud'S Disease
|
Raynaud Phenomenon
|
|
Raynaud'S Syndrome
|
Raynaud'S
|
|
Cold Fingers, Hereditary
|
Raynaud'S Phenomenon
|
|
Raynaud'S Disease/Phenomenon
|
Raynauds Syndrome
|
|
Raynauds Phenomenon
|
Secondary Raynaud'S Phenomenon
|
|
Raynaud Syndrome
|
|
|
| Hepatopulmonary Syndrome |
|
|
| Microcephaly 4, Primary, Autosomal Recessive |
|
MCPH4
|
Primary Autosomal Recessive Microcephaly 4
|
|
Microcephaly, Primary Autosomal Recessive, 4
|
Microcephaly, Type 4, Primary, Autosomal Recessive
|
|
|
| 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
|
|
|
| Coronary Stenosis |
|
|
| Acute Myocardial Infarction |
|
Cardiac Attack
|
Heart Attack
|
|
|
| Hyperhomocysteinemia |
|
|
| Atrial Fibrillation |
|
A-Fib
|
Fibrillation, Atrial
|
|
Af - [Atrial Fibrillation]
|
Rapid Atrial Fibrillation
|
|
A Fib - [Atrial Fibrillation]
|
|
|
| Brachydactyly, Type D |
|
Brachydactyly Type D
|
BDD
|
|
Stub Thumb
|
Brachydactyly D
|
|
|
| Collagen Disease |
|
Collagen Diseases
|
Collagen Disorder
|
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| Active Peptic Ulcer Disease |
|
Gi Bleeding
|
Active Peptic Ulcer
|
|
Gastrointestinal Hemorrhage
|
|
|
| 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
|
|
|
| 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
|
|
|
| Vascular Cancer |
|
Blood Vessel Tumors
|
Malignant Vascular Neoplasm
|
|
Renal Vein Leiomyosarcoma
|
Vascular Neoplasms
|
|
Blood Vessel Neoplasm
|
Blood Vessel Tumor
|
|
Blood Vessel Tumour Disorder
|
Haemangiomatous Tumour
|
|
Leiomyosarcoma Of The Renal Vein
|
Malignant Great Vessel Tumor
|
|
Malignant Tumor Of Pulmonary Artery
|
Malignant Tumor Of Pulmonary Vein
|
|
Malignant Vascular Tumor
|
Neoplasm Of Great Vessel
|
|
Pulmonary Artery Malignant Neoplasm
|
Pulmonary Vein Malignant Neoplasm
|
|
Vascular Tissue Neoplasm
|
Vascular Tumors
|
|
Blood Vessel Cancer
|
Neoplasms, Vascular Tissue
|
|
Malignant Neoplasm Of Great Vessels
|
|
|
| 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
|
|
|
| Retinal Vein Occlusion |
|
Occlusion, Of Retinal Vein
|
|
|
| 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
|
|
|
| Impotence |
|
Erectile Dysfunction
|
Sexual Impotence
|
|
Erectile Dysfunction Adverse Event
|
|
|
| Thrombocytosis |
|
|
| 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
|
|
|
| Diabetes Insipidus |
|
|
| Atherosclerosis Susceptibility |
|
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
|
Alp
|
Arteriosclerosis
|
|
|
| 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
|
|
|
| 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
|
|
|
| Splenic Sequestration |
|
|
| Hyaline Fibromatosis Syndrome |
|
Juvenile Hyaline Fibromatosis
|
Inherited Systemic Hyalinosis
|
|
Puretic Syndrome
|
Infantile Systemic Hyalinosis
|
|
HFS
|
Hyalinosis, Systemic
|
|
Systemic Hyalinosis
|
Molluscum Fibrosum
|
|
Murray Syndrome
|
Murray-Puretic-Drescher Syndrome
|
|
Ish
|
Jhf
|
|
Fibromatosis, Juvenile Hyaline
|
Hyalinosis, Systemic Infantile
|
|
Fibromatosis, Hyaline Syndrome
|
Neurofibromatosis 1
|
|
|
| Hypothyroidism |
|
Thyroid Diseases
|
Thyroid Disease
|
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
|
Dysfunction Thyroid
|
Thyroid Dysfunction
|
|
|
| Nonbacterial Thrombotic Endocarditis |
|
Non-Bacterial Thrombotic Endocarditis
|
Marantic Endocarditis
|
|
Non-Infective Endocarditis
|
|
|
| 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
|
|
|
| Alcoholic Hepatitis |
|
Acute Alcoholic Hepatitis
|
Acute Alcoholic Liver Disease
|
|
Hepatitis, Alcoholic
|
Hepatitis Alcoholic
|
|
Ah - [Alcoholic Hepatitis]
|
Ethanol Hepatitis
|
|
|
| Angiosarcoma |
|
|
| Hyperthyroidism |
|
|
| 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
|
|
|
| Arthritis |
|
Inflammatory Joint Disease
|
Inflammatory Disorder Of Joint
|
|
|
| Hemangioma |
|
|
| Hydronephrosis |
|
Stricture Of Ureteropelvic Junction With Hydronephrosis
|
Hydronephrosis With Ureteral Stricture, Not Elsewhere Classified
|
|
|
| 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
|
|
|
| Congestive Heart Failure |
|
Congestive Heart Disease
|
Heart Failure
|
|
Cardiac Failure Congestive
|
Chf
|
|
Weak Heart
|
Heart Failure Congestive
|
|
Ccf - [Congestive Cardiac Failure]
|
Chf - [Congestive Heart Failure]
|
|
Congestive Cardiac Diseases
|
Congested Heart Failure
|
|
Congestive Cardiac Failure
|
Cardiac Anasarca
|
|
Cardiac Oedema
|
Cardiac Stasis
|
|
Cardiovascular Oedema
|
Cardiac Hydrops
|
|
Congestive Failure
|
Heart Congestion
|
|
Heart Fluid
|
Oedematous Heart
|
|
|
| Carotid Artery Thrombosis |
|
|
| 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
|
|
|
| Post-Thrombotic Syndrome |
|
Postphlebitic Syndrome
|
Postthrombotic Syndrome
|
|
Postphlebetic Syndrome With Inflammation
|
Postphlebetic Syndrome With Ulcer
|
|
Postphlebetic Syndrome With Ulcer And Inflammation
|
Venous Stress Disorder
|
|
|
| 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
|
|
|
| Lymphangiosarcoma |
|
Skin Lymphangiosarcoma
|
Stewart Treves Syndrome
|
|
Lymphangiosarcoma Of Stewart And Treves
|
Malignant Lymphangioendothelioma
|
|
Stewart-Treves Syndrome
|
|
|
| Myeloproliferative Neoplasm |
|
Myeloproliferative Disorder
|
Chronic Myeloproliferative Disease
|
|
Myeloproliferative Neoplasms
|
Chronic Myeloproliferative Disorder
|
|
Cmpd
|
Cmpd, U
|
|
Chronic Myeloproliferative Disorders
|
Mpd
|
|
Mpn
|
Myeloproliferative Disorders
|
|
Myeloproliferative Disease
|
Campomelic Dysplasia
|
|
|
| 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
|
|
|
| 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
|
|
|
| Hepatic Vascular Disease |
|
Vascular Disorder Of Liver
|
|
|
| Limb Ischemia |
|
|
| 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
|
|
|
| Intracranial Embolism |
|
Cerebral Embolism
|
Cerebral Embolism With Cerebral Infarction
|
|
|
| Generalized Atherosclerosis |
|
Generalised Atherosclerosis
|
|
|
| Vein Disease |
|
|
| 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]
|
|
|
| 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]
|
|
|
| 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
|
|
|
| Medulloadrenal Hyperfunction |
|
|
| Deafness, Autosomal Recessive 110 |
|
DFNB110
|
Autosomal Recessive Nonsyndromic Deafness 110
|
|
Autosomal Recessive Deafness 110
|
Deafness, Autosomal Recessive, 110
|
|
|
| Endocardium Disease |
|
|
| Bleeding Disorder, Platelet-Type, 11 |
|
BDPLT11
|
Glycoprotein Vi Deficiency
|
|
Gp Vi Deficiency
|
Platelet-Type Bleeding Disorder 11
|
|
Bleeding Diathesis Due To A Collagen Receptor Defect
|
Bleeding Diathesis Due To Glycoprotein Vi Deficiency
|
|
Platelet-Type Bleeding Disorder-11
|
Bleeding Disorder, Platelet Type 11
|
|
Hemorrhage
|
|
|
| Aortic Valve Disease 1 |
|
Aortic Valve Disease
|
Bicuspid Aortic Valve
|
|
Aortic Valve Disorder
|
AOVD1
|
|
Bav
|
Bicuspid Aortic Valve Disease
|
|
Familial Bicuspid Aortic Valve
|
Aortic Valve Calcification
|
|
Aovd
|
Aortic Valve, Bicuspid
|
|
Aortic Valve, Calcification Of
|
Aortic Stenosis, Calcific
|
|
Familial Bav
|
Calcific Aortic Stenosis
|
|
Calcification Of Aortic Valve
|
Abnormality Of The Aortic Valve
|
|
Aortic Valve Disease, Type 1
|
Aortic Valve Disease 2
|
|
Bicommissural Aortic Valve
|
|
|
| Infective Endocarditis |
|
Bacterial Endocarditis
|
Endocarditis, Infective
|
|
Infectious Endocarditis
|
Endocarditis Infective
|
|
|
| Carotid Artery Disease |
|
Carotid Artery Diseases
|
Disorder Of Carotid Artery
|
|
|
| Temporal Arteritis |
|
Polymyalgia Rheumatica
|
Giant Cell Arteritis
|
|
Cranial Arteritis
|
Horton Disease
|
|
Gca
|
Horton'S Disease
|
|
Rhizomelic Pseudopolyarthritis
|
Arteritis Cranialis
|
|
Arteritis Temporalis
|
Horton'S Arteritis
|
|
Horton'S Giant Cell Arteritis
|
Horton'S Temporal Arteritis
|
|
Horton'S Syndrome
|
Gca - [Giant Cell Arteritis]
|
|
Senile Arthritis
|
Polymyalgia Arteritica
|
|
Pmr - [Polymyalgia Rheumatica]
|
Forestier-Certonciny Syndrome
|
|
Rheumatic Polymyalgia
|
Polymyalgia
|
|
|
| Kidney Disease |
|
Renal Failure
|
Kidney Failure
|
|
Kidney Diseases
|
Nephropathy
|
|
Abnormality Of The Kidney
|
Impaired Renal Function Disease
|
|
Renal Anomaly
|
Kidney Dysfunction
|
|
Renal Disease
|
Nephropathies
|
|
Renal Failure Adverse Event
|
Abnormal Renal Function
|
|
|
| Primary Thrombocytopenia |
|
|
| Glycogen Storage Disease |
|
Glycogenosis
|
Glycogenoses
|
|
Gsd
|
Storage Disease, Glycogen
|
|
Gsd - [Glycogen Storage Disease]
|
Glycogen Thesaurismosis
|
|
Diffuse Glycogenosis
|
Generalised Glycogen Storage Disease
|
|
Generalised Glycogenosis
|
Generalised Glycogen Storage Disease Of Infants
|
|
Glycogen Synthase Deficiency
|
|
|
| Chronic Venous Insufficiency |
|
|
| Cardiomyopathy, Familial Hypertrophic, 20 |
|
Hypertrophic Cardiomyopathy 20
|
CMH20
|
|
Cardiomyopathy, Hypertrophic, 20
|
Cardiomyopathy Familial Hypertrophic 20
|
|
Cardiomyopathy, Familial Hypertrophic 20
|
Cardiomyopathy, Hypertrophic, Familial, Type 20
|
|
|
| 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
|
|
|
| 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
|
|
|
| Diarrhea |
|
Diarrhoea
|
Diarrhea Of Presumed Infectious Origin
|
|
|
| Arteriovenous Malformation |
|
Arteriovenous Malformations
|
Arteriovenous Hemangioma
|
|
Cirsoid Aneurysm
|
Racemose Aneurysm
|
|
Racemose Angioma
|
Racemose Hemangioma
|
|
Congenital Arteriovenous Malformation
|
|
|
| Aortic Valve Disease 2 |
|
Aortic Valve Stenosis
|
Aortic Stenosis
|
|
Rheumatic Aortic Stenosis
|
AOVD2
|
|
Bicuspid Aortic Valve
|
Rheumatic Aortic Valve Stenosis
|
|
Valvular Aortic Stenosis
|
Aortic Valve Disease, Type 2
|
|
Aortic Valve Stricture
|
Aortic Valve Obstruction
|
|
Obstructed Aorta Valve
|
Rheumatic Aortic Obstruction
|
|
Rheumatic Aortic Valve Obstruction
|
Rheumatic Aortic Stricture
|
|
Aortic Valve Regurgitation
|
Aortic Insufficiency With Stenosis
|
|
Rheumatic Aortic Valve Stenosis With Insufficiency
|
Rheumatic Aortic Stenosis With Incompetence
|
|
Rheumatic Aortic Stenosis With Regurgitation
|
|
|
| Autoimmune Disease Of Cardiovascular System |
|
|
| Capillary Lymphangioma |
|
Microcystic Lymphatic Malformation
|
Capillary Lymphatic Malformation
|
|
Microcystic Infiltrating Lymphatic Malformation
|
Microcystic Lymphangioma
|
|
Superficial Lymphangioma
|
Cutaneous Lymphangioma Circumscriptum
|
|
Superficial Lymphatic Malformation
|
Cutaneous Lymphangioma
|
|
Lymphangioma Of Skin
|
Lymphangioma Circumscriptum
|
|
|
| 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
|
|
|
| Deafness, Autosomal Dominant 9 |
|
DFNA9
|
Autosomal Dominant Nonsyndromic Deafness 9
|
|
Autosomal Dominant Deafness 9
|
Deafness, Autosomal Dominant, 9
|
|
Deafness, Autosomal Dominant, Type 9
|
|
|
| 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
|
|
|
| Heart Valve Disease |
|
Heart Valve Diseases
|
Valvular Heart Disease
|
|
Valvular Heart Diseases
|
Heart Valve Prolapse
|
|
|
| Peripheral Artery Disease |
|
Peripheral Arterial Disease
|
Peripheral Arterial Diseases
|
|
|
| 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
|
|
|
| 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]
|
|
|
| Long Covid |
|
Post-Acute Sequelae Of Sars-Cov-2 Infection
|
Chronic Covid-19
|
|
Pasc
|
Post-Covid Syndrome
|
|
|
| Severe Covid-19 |
|
|
| Diabetic Angiopathy |
|
Diabetic Angiopathies
|
Diabetic Peripheral Angiopathy
|
|
Diabetic Vascular Disorder
|
|
|
| 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
|
|
|
| Cavernous Hemangioma |
|
Hemangioma, Cavernous
|
Cavernoma
|
|
Cavernous Haemangioma
|
|
|
| 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
|
|
|
| Blood Protein Disease |
|
Blood Protein Disorders
|
Blood Protein Disorder
|
|
|
| Coronavirus Infectious Disease |
|
|
| Autoimmune Disease Of Blood |
|
|
| Aortic Disease |
|
Aortic Diseases
|
Aortic Disorder
|
|
Disorder Of The Aorta
|
|
|
| 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
|
|
|
| Infiltrating Angiolipoma |
|
Angiolipoma, Infiltrating
|
|
|
| Pyogenic Granuloma |
|
Lobular Capillary Hemangioma
|
Granuloma Pyogenic
|
|
Granuloma Pyogenicum
|
Granuloma Telangiectaticum Of Skin
|
|
Pyogenic Granuloma Of Skin
|
Lobular Capillary Haemangioma Of Skin
|
|
|
| Diabetes Mellitus |
|
|
| Chronic Kidney Disease |
|
Chronic Renal Disease
|
Chronic Kidney Failure
|
|
Ckd
|
Chronic Renal Failure
|
|
Kidney Failure, Chronic
|
Chronic Renal Failure Syndrome
|
|
Crf
|
Renal Failure - Chronic
|
|
Renal Failure Chronic
|
Chronic Kidney Diseases
|
|
Chronic Kidney Disease Stage 5
|
Ckd - [Chronic Kidney Disease]
|
|
Crf - [Chronic Renal Failure]
|
Chronic Kidney Impairment
|
|
Chronic Renal Impairment
|
Chronic Kidney Shutdown
|
|
Chronic Hypoxic Kidney Failure
|
Chronic Kidney Collapse
|
|
Chronic Renal Insufficiency
|
Chronic Kidney Toxaemia
|
|
Chronic Kidney Hypofunction
|
Chronic Renal Suppression
|
|
Chronic Renal Failure, Stage 5
|
Ckd - [Chronic Kidney Disease] Stage 5
|
|
End Stage Kidney Failure
|
End Stage Renal Failure
|
|
End Stage Kidney Disease
|
End Stage Renal Disease
|
|
End Stage Chronic Renal Failure
|
Esrf - [End Stage Renal Failure]
|
|
Esrd - [End Stage Renal Diseases]
|
Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
|
|
|
| Scoliosis |
|
|
| 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
|
|
|
| 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
|
|
|
| Complement Component 2 Deficiency |
|
C2D
|
C2 Deficiency
|
|
Complement 2 Deficiency
|
Complement Component-2
|
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| 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]
|
|
|
| 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
|
|
|
| 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
|
|
|
| Stickler Syndrome, Type I |
|
Stickler Syndrome 1
|
Stickler Syndrome Type 1
|
|
STL1
|
Aom
|
|
Stickler Syndrome, Type 1
|
Stickler Syndrome, Vitreous Type 1
|
|
Stickler Syndrome, Membranous Vitreous Type
|
Arthroophthalmopathy, Hereditary Progressive
|
|
Arthro-Ophthalmopathy Hereditary Progressive
|
Stickler Syndrome Membranous Vitreous Type
|
|
Stickler Syndrome Type I
|
Stickler Syndrome Vitreous Type 1
|
|
|
| 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
|
|
|
| Hermansky-Pudlak Syndrome |
|
Hps
|
Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells
|
|
Hermanski-Pudlak Syndrome
|
Hermansky Pudlak Syndrome
|
|
Platelet Storage Pool Deficiency
|
|
|
| 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
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Bilirubin Metabolic Disorder |
|
Hyperbilirubinemia
|
Hereditary Hyperbilirubinemia
|
|
Hyperbilirubinemia, Hereditary
|
Hyperbilirubinaemia
|
|
|
| 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
|
|
|
| Dilated Cardiomyopathy |
|
Familial Dilated Cardiomyopathy
|
Primary Dilated Cardiomyopathy
|
|
Idiopathic Dilated Cardiomyopathy
|
Congestive Cardiomyopathy
|
|
Idiopathic Dilation Cardiomyopathy
|
Primary Familial Dilated Cardiomyopathy
|
|
Cardiomyopathy, Dilated
|
DCM
|
|
Cardiomyopathy, Familial Dilated
|
Dilated Cardiomyopathy, Familial
|
|
Hypokinetic Dilated Cardiomyopathy, Familial
|
Familial Idiopathic Cardiomyopathy
|
|
Fdc
|
Cardiomyopathy, Familial Idiopathic
|
|
Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
|
Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
|
Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
|
Dilated-Hypokinetic Cardiomyopathy
|
Congestive Idiopathic Cardiomyopathy
|
|
Primary Idiopathic Dilated Cardiomyopathy
|
|
|
