| 疾病名称 |
别名 |
|
| 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
|
|
|
| Thrombosis |
|
Thrombosis Of Blood Vessel
|
|
|
| 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
|
|
|
| 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
|
|
|
| Sagittal Sinus Thrombosis |
|
Thrombosis Of Superior Longitudinal Sinus
|
Thrombosis Of Superior Sagittal Sinus
|
|
Thrombosis Superior Sagittal Sinus
|
|
|
| Protein S Deficiency |
|
Protein S Deficiency Disease
|
Hereditary Thrombophilia Due To Protein S Deficiency
|
|
|
| Pulmonary Embolism |
|
Pulmonary Artery Embolism
|
Pulmonary Embolus
|
|
Pulmonary Emboli
|
|
|
| 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
|
|
|
| Protein C Deficiency |
|
Hereditary Thrombophilia Due To Protein C Deficiency
|
Proc Deficiency
|
|
Congenital Thrombotic Disease, Due To Protein C Deficiency
|
|
|
| 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
|
|
|
| Thrombophilia |
|
|
| Intracranial Thrombosis |
|
Cerebral Thrombosis
|
Thrombosis Of Cerebral Veins
|
|
Cerebral Arterial Thrombosis
|
|
|
| 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
|
|
|
| Placental Abruption |
|
Abruptio Placentae
|
Abruptio Placenta
|
|
Abortion, Threatened
|
Threatened Miscarriage
|
|
Haemorrhage Specified As Due To Threatened Abortion
|
Spontaneous Threatened Abortion
|
|
|
| Purpura Fulminans |
|
|
| 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
|
|
|
| Congenital Disorder Of Glycosylation, Type Ia |
|
CDG1A
|
Cdg Ia
|
|
Phosphomannomutase 2 Deficiency
|
Jaeken Syndrome
|
|
Pmm2-Congenital Disorder Of Glycosylation
|
Congenital Disorder Of Glycosylation Type Ia
|
|
Cdgia
|
Congenital Disorder Of Glycosylation Ia
|
|
Congenital Disorder Of Glycosylation 1a
|
Carbohydrate-Deficient Glycoprotein Syndrome Type Ia
|
|
Cdgs1a
|
Pmm2-Cdg
|
|
Cdg-Ia
|
Congenital Disorder Of Glycosylation Type 1a
|
|
Carbohydrate-Deficient Glycoprotein Syndrome, Type Ia, Formerly
|
Pmm Deficiency
|
|
Cdg Syndrome Type Ia
|
Carbohydrate Deficient Glycoprotein Syndrome Type Ia
|
|
Cdg Syndrome Type 1a
|
Jaeken'S Syndrome
|
|
Pmm2 Deficiency
|
Glycosylation, Congenital Disorder Of, Type Ia
|
|
|
| Post-Thrombotic Syndrome |
|
Postphlebitic Syndrome
|
Postthrombotic Syndrome
|
|
Postphlebetic Syndrome With Inflammation
|
Postphlebetic Syndrome With Ulcer
|
|
Postphlebetic Syndrome With Ulcer And Inflammation
|
Venous Stress Disorder
|
|
|
| Coronary Thrombosis |
|
Coronary Artery Thrombosis
|
|
|
| Legg-Calve-Perthes Disease |
|
Perthes Disease
|
LCPD
|
|
Coxa Plana
|
Legg-Perthes Disease
|
|
Juvenile Osteochondrosis Of Hip And Pelvis
|
Pseudocoxalgia
|
|
Legg-Calvé-Perthes Disease
|
Lcp
|
|
Calve - Perthes' Disease
|
Juvenile Osteochond-Hip/Pelvis
|
|
Juvenile Osteochondrosis Of Hip And/Or Pelvis
|
Legg-Calve-Perthes Symptom
|
|
Osteochondrosis Of Legg-Calve-Perthes
|
Perthe'S Disease
|
|
Legg-Calve-Perthes Syndrome
|
Osteochondritis Deformans
|
|
Calve-Perthes Disease
|
Aseptic Necrosis Of The Capital Femoral Epiphysis
|
|
Osteochondrosis Of The Capital Femoral Epiphysis
|
Legg-Calvé-Perthes Syndrome
|
|
Avascular Necrosis Of The Capital Femoral Epiphysis
|
|
|
| Sneddon Syndrome |
|
Livedo Reticularis And Cerebrovascular Accidents
|
SNDNS
|
|
Ehrmann-Sneddon Syndrome
|
Livedo Racemosa-Cerebrovascular Accident Syndrome
|
|
Livedo Reticularis-Cerebrovascular Accident Syndrome
|
Sneddon'S Syndrome
|
|
Idiopathic Livedo Reticularis With Systemic Involvement
|
Cerebro-Vascular Lesions And Livedo Reticularis
|
|
Livedo Racemosa And Cerebrovascular Accidents
|
|
|
| Retinal Vein Occlusion |
|
Occlusion, Of Retinal Vein
|
|
|
| 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
|
|
|
| Purpura |
|
|
| 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
|
|
|
| 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
|
|
|
| Hyperhomocysteinemia |
|
|
| 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
|
|
|
| Retinal Artery Occlusion |
|
Retina Artery Narrowing
|
Retinal Artery Spasm
|
|
Spasm Of Ophthalmic Artery
|
Retinal Spasm
|
|
Vasospasm Of Retina
|
|
|
| Intracranial Sinus Thrombosis |
|
Sinus Thrombosis, Intracranial
|
|
|
| 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
|
|
|
| Thrombocytosis |
|
|
| Varicose Veins |
|
Varices
|
Varix
|
|
Venous Ectasia
|
Venous Varices
|
|
Varicosity
|
|
|
| Eclampsia |
|
Eclampsia In Puerperium
|
Postpartum Eclampsia
|
|
Eclampsia, Postpartum
|
Puerperal Eclampsia
|
|
|
| Central Retinal Vein Occlusion |
|
|
| Pulmonary Artery Disease |
|
Abnormality Of The Pulmonary Artery
|
|
|
| Homocystinuria |
|
Cystathionine Beta Synthase Deficiency
|
Homocysteinemia
|
|
Cbs Deficiency
|
Cystathionine Synthase Deficiency
|
|
Cystathionine Beta-Synthase Deficiency Disease
|
|
|
| Factor Xi Deficiency |
|
Plasma Thromboplastin Antecedent Deficiency
|
Rosenthal Syndrome
|
|
Pta Deficiency
|
Hemophilia C
|
|
Rosenthal Factor Deficiency
|
F11 Deficiency
|
|
Congenital Factor Xi Deficiency
|
Hereditary Factor Xi Deficiency Disease
|
|
Haemophilia C
|
Factor Xi Deficiency, Autosomal Dominant
|
|
Rosenthal'S Disease
|
Factor 11 Deficiency
|
|
Factor Xi
|
Factor Xi Deficiency, Autosomal Recessive
|
|
Factor Xi Deficiency, Congenital
|
FA11D
|
|
Thromboplastin Antecedent Deficiency
|
Pta - [Plasma Thromboplastin Antecedent] Deficiency
|
|
Congenital Factor Xi Deficiency Disease
|
Rosenthal Disease
|
|
|
| Hypersplenism |
|
Hypersplenia
|
Big Spleen Syndrome
|
|
Hyperfunction Of Spleen
|
Increased Splenic Activity
|
|
Spleen Metaplasia
|
Splenic Metaplasia
|
|
|
| Blood Protein Disease |
|
Blood Protein Disorders
|
Blood Protein Disorder
|
|
|
| Liver Cirrhosis |
|
Cirrhosis
|
Cirrhosis Of Liver
|
|
CIRRH
|
Cryptogenic Cirrhosis
|
|
Cirrhosis, Cryptogenic
|
Cirrhosis Nos
|
|
|
| Afibrinogenemia, Congenital |
|
Congenital Afibrinogenemia
|
Afibrinogenemia
|
|
Factor I Deficiency
|
Familial Afibrinogenemia
|
|
Hypofibrinogenemia, Congenital
|
Fibrinogen Deficiency
|
|
Afibrinogenemia Congenital
|
CAFBN
|
|
Congenital Hypofibrinogenemia
|
Hypofibrinogenemia
|
|
Complement Factor I Deficiency
|
|
|
| Vulvar Angiokeratoma |
|
Fordyce Angiokeratoma Of Vulva
|
Angiokeratoma Of Vulva
|
|
|
| Myocardial Stunning |
|
|
| 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
|
|
|
| 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]
|
|
|
| Coronary Restenosis |
|
|
| Endocarditis |
|
|
| Acute Myocardial Infarction |
|
Cardiac Attack
|
Heart Attack
|
|
|
| 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
|
|
|
| Placenta Disease |
|
Placenta Diseases
|
Placenta Disorder
|
|
Pregnancy Complications
|
Placenta Disorders
|
|
|
| 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
|
|
|
| Dysfibrinogenemia, Congenital |
|
Dysfibrinogenemia
|
Hypodysfibrinogenemia
|
|
Familial Dysfibrinogenemia
|
Familial Hypodysfibrinogenemia
|
|
Hypodysfibrinogenemia, Congenital
|
Dysfibrinogenemia, Familial
|
|
Congenital Dysfibrinogenemia
|
DYSFIBRIN
|
|
|
| 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
|
|
|
| Thoracic Outlet Syndrome |
|
Tos
|
Tos - Thoracic Outlet Syndrome
|
|
Thoracic Outlet Syndromes
|
Thoracic Outlet Compression Syndrome
|
|
|
| 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
|
|
|
| Intermittent Claudication |
|
Charcot'S Syndrome
|
Amyotrophic Lateral Sclerosis
|
|
|
| Fibrinolytic Defect |
|
|
| Blood Platelet Disease |
|
Platelet Disorder
|
Blood Platelet Disorders
|
|
Thrombocytopathy
|
Platelet Dysfunction
|
|
Platelet Disorders
|
Qualitative Platelet Deficiency
|
|
|
| Branch Retinal Artery Occlusion |
|
Retinal Artery Occlusion
|
Arterial Retinal Branch Occlusion
|
|
Retinal Arterial Branch Occlusion
|
|
|
| Cavernous Sinus Thrombosis |
|
Thrombosis Of Cavernous Venous Sinus
|
|
|
| Vein Disease |
|
|
| Hemoglobinuria |
|
|
| 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
|
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
| 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
|
|
|
| Nonbacterial Thrombotic Endocarditis |
|
Non-Bacterial Thrombotic Endocarditis
|
Marantic Endocarditis
|
|
Non-Infective Endocarditis
|
|
|
| Myocardial Infarction |
|
Heart Attack
|
Myocardial Infarction, Susceptibility To
|
|
Myocardial Infarction 1
|
Myocardial Infarction, Protection Against
|
|
Myocardial Infarction, Decreased Susceptibility To
|
Myocardial Infarction, Decreased
|
|
Myocardial Infarct
|
MCI1
|
|
Premature Myocardial Infarction
|
Myocardial Infarction, Susceptibility To, Type 1
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| 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
|
|
|
| Hepatic Vascular Disease |
|
Vascular Disorder Of Liver
|
|
|
| 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]
|
|
|
| Alpha-1-Antitrypsin Deficiency |
|
Alpha 1-Antitrypsin Deficiency
|
Alpha-1 Antitrypsin Deficiency
|
|
Aat Deficiency
|
Aatd
|
|
A1ATD
|
Emphysema Due To Aat Deficiency
|
|
A1at Deficiency
|
Emphysema-Cirrhosis, Due To Aat Deficiency
|
|
Hemorrhagic Diathesis Due To Antithrombin Pittsburgh
|
Alpha-1 Antiprotease Deficiency
|
|
Alpha 1 Antitrypsin Deficiency
|
Aat
|
|
Alpha-1 Protease Inhibitor Deficiency
|
Alpha-1 Related Emphysema
|
|
Genetic Emphysema
|
Hereditary Pulmonary Emphysema
|
|
Inherited Emphysema
|
Alpha-1-Proteinase Inhibitor Deficiency
|
|
Alpha1-Antitrypsin Deficiency
|
Alpha-1-Antitrypsin Deficiency, Autosomal Recessive
|
|
Emphysema, Hereditary Pulmonary
|
Aatd - [Alpha-1-Antitrypsin] Deficiency
|
|
|
| Ovarian Hyperstimulation Syndrome |
|
OHSS
|
Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous
|
|
Secondary Meig'S Syndrome
|
Ohss - [Ovarian Hyperstimulation Syndrome]
|
|
Hyperstimulation Of Ovaries Nos
|
Hyperstimulation Of Ovaries Associated With Induced Ovulation
|
|
|
| Dic In Newborn |
|
Disseminated Intravascular Coagulation In Newborn
|
|
|
| Preeclampsia/Eclampsia 1 |
|
PEE1
|
Preg1
|
|
Pee
|
Toxemia Of Pregnancy
|
|
Pregnancy Toxemias
|
Preeclampsia/Eclampsia, Type 1
|
|
Pre-Eclampsia
|
|
|
| Heparin Cofactor Ii Deficiency |
|
Thrombophilia Due To Heparin Cofactor Ii Deficiency
|
THPH10
|
|
Hcf Ii Deficiency
|
Hcf2 Deficiency
|
|
Thrombophilia 10 Due To Heparin Cofactor Ii Deficiency
|
Hcf 2 Deficiency
|
|
Thrombophilia Due To Heparin Cofactor 2 Deficiency
|
Thrombophilia, Due To Heparin Cofactor Ii Deficiency
|
|
|
| Pulmonary Edema |
|
|
| Autoimmune Disease Of Cardiovascular System |
|
|
| Placental Insufficiency |
|
Uteroplacental Vascular Insufficiency
|
|
|
| Mastoiditis |
|
|
| Nephrotic Syndrome |
|
Finnish Congenital Nephrotic Syndrome
|
Ns - [Nephrotic Syndrome]
|
|
Nephrosis Syndrome
|
Nephrosis Nos
|
|
Glomerular Lesion Nephrosis
|
|
|
| Congenital Disorder Of Glycosylation, Type Ib |
|
CDG1B
|
Cdg Ib
|
|
Cdgib
|
Mannosephosphate Isomerase Deficiency
|
|
Mpi Deficiency
|
Protein-Losing Enteropathy-Hepatic Fibrosis Syndrome
|
|
Saguenay-Lac Saint-Jean Syndrome
|
Slsj Syndrome
|
|
Congenital Disorder Of Glycosylation Ib
|
Congenital Disorder Of Glycosylation 1b
|
|
Mpi-Cdg
|
Cdg-Ib
|
|
Congenital Disorder Of Glycosylation Type 1b
|
Congenital Disorder Of Glycosylation Type Ib
|
|
Cdg, Gastrointestinal Type
|
Cdg Syndrome Type Ib
|
|
Carbohydrate Deficient Glycoprotein Syndrome Type Ib
|
Phosphomannose Isomerase Deficiency
|
|
Carbohydrate-Deficient Glycoprotein Syndrome Type Ib
|
Cdg Gastrointestinal Type
|
|
Cdgs1b
|
Glycosylation, Congenital Disorder Of, Type Ib
|
|
|
| Acute Vascular Insufficiency Of Intestine |
|
Acute Gastrointestinal Tract Vascular Insuffic.
|
Acute Git Vascular Insuffic.
|
|
Acute Intestinal Ischemia
|
Acute Intestinal Vascular Insufficiency
|
|
|
| Prothrombin Deficiency |
|
Factor Ii Deficiency
|
Hypoprothrombinemia
|
|
Dysprothrombinemia
|
Deficiency, Prothrombin
|
|
Inherited Factor Ii Deficiency
|
Hereditary Factor Ii Deficiency Disease
|
|
|
| Intracranial Embolism |
|
Cerebral Embolism
|
Cerebral Embolism With Cerebral Infarction
|
|
|
| Nonarteritic Anterior Ischemic Optic Neuropathy |
|
Anterior Ischemic Optic Neuropathy
|
Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To
|
|
NAION
|
Non-Arteritic Anterior Ischemic Optic Neuropathy
|
|
Ischemic Optic Neuropathy
|
Aion
|
|
Optic Neuropathy, Ischemic
|
Naion, Susceptibility To
|
|
Optic Neuropathy, Anterior Ischemic
|
Optic Neuropathy, Anterior Ischemic, Susceptibility To
|
|
Non-Arteritic Anterior Ischaemic Optic Neuropathy
|
Nonarteritic Anterior Ischaemic Optic Neuropathy
|
|
Neuropathy, Optic, Ischemic, Nonarteritic Anterior, Susceptibility To
|
Ion - [Ischemic Optic Neuropathy]
|
|
Neuropathic Ischaemia Of N.Opticus
|
Ischaemic Neuropathy Of Optic Nerve
|
|
|
| Toxic Shock Syndrome |
|
Septic Shock
|
Toxic Shock
|
|
Tss
|
Shock, Septic
|
|
Staphylococcal Toxic Shock Syndrome
|
Tss - [Toxic Shock Syndrome]
|
|
|
| Meningococcemia |
|
|
| Osteonecrosis |
|
Bone Necrosis
|
Avascular Necrosis Of Bone
|
|
Aseptic Necrosis
|
Necrosis Of Bone Nos
|
|
Aseptic Osteonecrosis
|
Aseptic Necrosis Of Bone, Site Unspecified
|
|
Aseptic Or Avascular Bone Necrosis
|
Aseptic Necrosis Of Bone
|
|
Necrotic Bone
|
Necrotizing Bone
|
|
Spontaneous Osteonecrosis
|
Osteoradionecrosis
|
|
|
| Splenic Infarction |
|
Splenic Infarct
|
Splenic Infarcts
|
|
Infarct Of The Spleen
|
|
|
| Platelet Aggregation, Spontaneous |
|
|
| 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
|
|
|
| Prothrombin Deficiency, Congenital |
|
Dysprothrombinemia
|
Hypoprothrombinemia
|
|
Congenital Factor Ii Deficiency
|
Prothrombin Deficiency
|
|
Factor Ii Deficiency
|
Congenital Prothrombin Deficiency
|
|
FA2D
|
Hypoprothrombinemias
|
|
Inherited Factor Ii Deficiency
|
Hereditary Factor Ii Deficiency Disease
|
|
|
| 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
|
|
|
| Intracranial Hypotension |
|
|
| Papilledema |
|
Choked Disk
|
Edema Of The Optic Disc
|
|
|
| Arteriosclerosis |
|
Arteriosclerotic Vascular Disease
|
|
|
| Retinal Vascular Occlusion |
|
Retinal Vasc. Occlusion
|
Occlusion Of Retinal Vessels
|
|
Retinal Obstruction
|
|
|
| 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
|
|
|
| Giant Hemangioma |
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| 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
|
|
|
| Lateral Sinus Thrombosis |
|
Thrombosis Of Lateral Venous Sinus
|
Thrombosis Transverse Sinus
|
|
|
| Compartment Syndrome |
|
Compartment Syndromes
|
Compartmental 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
|
|
|
| Encephalopathy, Familial, With Neuroserpin Inclusion Bodies |
|
Familial Encephalopathy With Neuroserpin Inclusion Bodies
|
FENIB
|
|
Encephalopathy, Familial, With Collins Bodies
|
Familial Dementia With Neuroserpin Inclusion Bodies
|
|
Familial Encephalopathy With Collins Bodies
|
|
|
| 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
|
|
|
| Chronic Venous Insufficiency |
|
|
| Vitamin K Deficiency Bleeding |
|
Vitamin K Deficiency
|
Deficiency Of Vitamin K
|
|
Vitamin K
|
Vitamin K Deficiency Hemorrhagic Disease
|
|
|
| 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
|
|
|
| Beta-Thalassemia |
|
Beta Thalassemia
|
Cooley'S Anemia
|
|
Mediterranean Anemia
|
Beta Thalassemia Intermedia
|
|
Erythroblastic Anemia
|
Thalassemia, Hispanic Gamma-Delta-Beta
|
|
Thalassemia Major
|
Thalassemia Minor
|
|
Beta-Plus-Thalassemia
|
Thalassemia, Beta
|
|
Beta Thalassemia Major
|
Beta Thalassemia Minor
|
|
Thalassemias, Beta-
|
Microcytemia, Beta Type
|
|
Thalassemia, Beta Type
|
B-THAL
|
|
Mediterranean Anaemia
|
Beta Thalassaemia Syndrome
|
|
Mediterranean Disease
|
Beta Thalassaemia Disease
|
|
|
| Plasminogen Deficiency, Type I |
|
Hypoplasminogenemia
|
Dysplasminogenemia
|
|
Plasminogen Deficiency Type I
|
Congenital Plasminogen Deficiency
|
|
Ligneous Conjunctivitis
|
Type 1 Plasminogen Deficiency
|
|
Plasminogen Deficiency Type 1
|
Plasminogen Deficiency
|
|
PLGD
|
Plasminogen Deficiency Type Ii
|
|
Deficiency, Plasminogen, Type I
|
|
|
| Central Retinal Artery Occlusion |
|
|
| Cholesterol Embolism |
|
Atheroembolism
|
Trash Foot
|
|
Cholesterol Crystal Embolism
|
Purple Toe Syndrome
|
|
Warfarin Blue Toe Syndrome
|
Embolism, Cholesterol
|
|
Cholesterol Embolus Syndrome
|
|
|
| Central Nervous System Origin Vertigo |
|
Vertigo Of Central Origin
|
Vertigo
|
|
Central Vestibular Vertigo
|
|
|
| Hepatic Coma |
|
Hepatic Encephalopathy
|
Hepatocerebral Intoxication
|
|
|
| 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 Infarction |
|
Infarct Of Liver
|
Hepatic Infarct
|
|
Liver Infarct
|
Liver Infarction
|
|
|
| Achenbach Syndrome |
|
Paroxysmal Hematoma Of The Finger
|
|
|
| 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
|
|
|
| Ischemic Colitis |
|
Colitis, Ischemic
|
Irreversible Ischaemic Colitis
|
|
|
| Abducens Palsy |
|
Sixth Nerve Palsy
|
Abducens Nerve Palsy
|
|
Abducens Nerve Disease
|
Abducens Nerve Weakness
|
|
Lateral Rectus Muscle Denervation Paresis
|
Lateral Rectus Muscle Innervation Disorder
|
|
Sixth Cranial Nerve Disorder
|
6th Nerve Palsy
|
|
Abducens Nerve Diseases
|
Vith Nerve Disorder
|
|
Vith Nerve Paralysis
|
Cranial Mononeuropathy Vi
|
|
Cranial Nerve Vi Palsy
|
Sixth Cranial Nerve Palsy
|
|
Vi Nerve Palsy
|
Abducens Nerve Disorder
|
|
Abducens Sixth Nerve Palsy
|
Abducens Nerve Paralysis
|
|
Disease Or Disorder Of Abducent Nerve
|
Sixth Cranial Nerve Disease
|
|
Sixth Cranial Nerve Weakness
|
Disorder Of Sixth Cranial Nerve
|
|
Isolated Abducent Nerve Palsy
|
Atrophy Of Sixth Cranial Nerve
|
|
Paralysis Of Sixth Cranial Nerve
|
|
|
| Protein-Losing Enteropathy |
|
Protein-Losing Enteropathies
|
Enteropathy, Exudative
|
|
Exudative Enteropathy
|
Ple - [Protein-Losing Enteropathy]
|
|
|
| Carotid Artery Thrombosis |
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Thrombophlebitis Migrans |
|
|
| 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
|
|
|
| Cavernous Hemangioma |
|
Hemangioma, Cavernous
|
Cavernoma
|
|
Cavernous Haemangioma
|
|
|
| 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
|
|
|
| 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]
|
|
|
| Buerger Disease |
|
Thromboangiitis Obliterans
|
Buerger'S Disease
|
|
Presenile Gangrene
|
Inflammatory Occlusive Peripheral Vascular Disease
|
|
Occlusive Peripheral Vascular Disease
|
Tao
|
|
Endarteritis Obliterans
|
|
|
| Cranial Nerve Palsy |
|
Cranial Nerve Paralysis
|
Cranial Nerve Diseases
|
|
Cranial Nerve Palsies
|
|
|
| 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 Hypertension |
|
Raised Intracranial Pressure
|
|
|
| Mild Pre-Eclampsia |
|
|
| Bacterial Sepsis |
|
|
| Amino Acid Metabolic Disorder |
|
Amino Acid Metabolism, Inborn Errors
|
Inborn Errors Of Amino Acid Metabolism
|
|
Disorder Of Amino Acid Metabolism
|
Amino Acid Metabolism Disorders
|
|
|
| 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
|
|
|
| Cerebral Palsy |
|
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
|
Palsy Cerebral
|
Palsy, Cerebral
|
|
Cerebral Palsy, Mixed
|
|
|
| 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
|
|
|
| Limb Ischemia |
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Endocardium Disease |
|
|
| Puerperal Pulmonary Embolism |
|
Obstetric Pulmonary Embolism
|
|
|
| Peripheral Vascular Disease |
|
Peripheral Arterial Disease
|
Arterial Occlusive Disease
|
|
Arterial Occlusive Diseases
|
Pad
|
|
Peripheral Vascular Diseases
|
Peripheral Occlusive Disease
|
|
Peripheral Arterial Diseases
|
Helicobacter Infections
|
|
|
| Carotid Artery Disease |
|
Carotid Artery Diseases
|
Disorder Of Carotid Artery
|
|
|
| Leukemia, Acute Lymphoblastic |
|
Acute Lymphoblastic Leukemia
|
ALL
|
|
Acute Lymphocytic Leukemia
|
Leukemia, Acute Lymphocytic, Susceptibility To, 1
|
|
Acute Lymphoblastic Leukaemia
|
Precursor Lymphoblastic Lymphoma/Leukemia
|
|
Precursor Lymphoid Neoplasm
|
Leukemia, Acute Lymphoblastic, Susceptibility To
|
|
B-Cell Acute Lymphoblastic Leukemia
|
Leukemia, Acute Lymphocytic 1
|
|
Acute Lymphocytic Leukaemia
|
Acute Lymphoblastic Leukemia/Lymphoma
|
|
All1
|
Childhood Acute Lymphoblastic Leukemia
|
|
Leukemia Acute Lymphoblastic 1
|
Leukemia Acute Lymphoblastic B-Hyperdiploid
|
|
Leukemia Acute Lymphocytic
|
Leukemia Acute Lymphocytic 1
|
|
Leukemia B-Cell Acute Lymphoblastic
|
Leukemia T-Cell Acute Lymphoblastic
|
|
Leukemia, Acute Lymphoblastic, 3
|
ALL3
|
|
Lymphoblastic Leukemia Acute
|
Leukemia, Acute, Lymphoblastic
|
|
Precursor Cell Lymphoblastic Leukemia Lymphoma
|
Leukemia, Lymphocytic, Acute, L1
|
|
Leukemia, Acute Lymphoblastic, Susceptibility To, 3
|
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| 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
|
|
|
| Hereditary Angioedema |
|
Hereditary Angioneurotic Edema
|
Hereditary Angioedema Type 1
|
|
Hane
|
Angioedema, Hereditary
|
|
Hae
|
Angioedemas, Hereditary
|
|
Deficiency Of C1 Esterase Inhibitor
|
C1 Esterase Inhibitor Deficiency
|
|
C1 Inhibitor Deficiency
|
Familial Angioneurotic Edema
|
|
Hereditary Bradykinine-Induced Angioedema
|
Hereditary Non Histamine-Induced Angioedema
|
|
Hae 1
|
Hae-I
|
|
Hereditary Angioneurotic Edema Type 1
|
Hereditary C1 Esterase Inhibitor Deficiency - Deficient Factor
|
|
Hereditary Angioedema Types I And Ii
|
Hereditary Angioneurotic Oedema
|
|
Familial Angioedema
|
Hae - [Hereditary Angioneurotic Oedema]
|
|
Bannister Disease, Hereditary
|
Quincke Disease Or Oedema
|
|
Hereditary Quincke Oedema
|
|
|
| Heart Septal Defect |
|
Septal Defect
|
Heart Septal Defects
|
|
Cardiac Septal Defects
|
Congenital Septal Defect Of Heart
|
|
|
| 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]
|
|
|
| Coronavirus Infectious Disease |
|
|
| Hemoglobin H Disease |
|
HBH
|
Hemoglobin H Disease, Nondeletional
|
|
Hemoglobin H Disease, Deletional
|
Alpha-Thalassemia Intermedia
|
|
Haemoglobin H Disease
|
Alpha-Thalassemia, Hemoglobin H Type
|
|
Hemoglobin H Disease, Deletional And Nondeletional
|
Alpha Thalassemia, Haemoglobin H Type
|
|
Alpha Thalassemia, Hemoglobin H Type
|
Haemoglobin H Disease, Deletional
|
|
Hbh Disease
|
Alpha-Thalassemia Hemoglobin H Type
|
|
Hemoglobin H Disease Deletional
|
Hemoglobin H Disease Non-Deletional
|
|
Alpha-Thalassemia
|
Alpha - /- - Or Mutational Forms Of Alpha-Thalassaemia
|
|
Alpha Thalassaemia Intermedia
|
|
|
| Inflammatory Bowel Disease |
|
Inflammatory Bowel Diseases
|
Bowel Disease, Inflammatory
|
|
|
| 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
|
|
|
| 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 |
|
|
| Gastroduodenal Crohn'S Disease |
|
|
| Klippel-Trenaunay-Weber Syndrome |
|
Klippel-Trenaunay Syndrome
|
KTS
|
|
Ktw Syndrome
|
Angioosteohypertrophy Syndrome
|
|
Angio-Osteohypertrophy Syndrome
|
Klippel Trenaunay Syndrome
|
|
Klippel-Trénaunay-Weber Syndrome
|
Haemangiectatic Hypertrophy
|
|
Weber-Klippel-Trenaunay
|
Congenital Dysplastic Angiopathy
|
|
Klippel-Trenaunay Disease
|
Weber Klippel Trenaunay
|
|
|
| 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
|
|
|
| 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
|
|
|
| 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
|
|
|
| Congenital Disorder Of Glycosylation, Type In |
|
Congenital Disorder Of Glycosylation
|
CDG1N
|
|
Congenital Disorders Of Glycosylation
|
Cdg In
|
|
Cdgin
|
Congenital Disorder Of Glycosylation 1n
|
|
Carbohydrate-Deficient Glycoprotein Syndrome
|
Cdg
|
|
Rft1-Cdg
|
Cdg-In
|
|
Congenital Disorder Of Glycosylation Type In
|
Carbohydrate Deficient Glycoprotein Syndrome
|
|
Cdg Syndrome
|
Congenital Disorder Of Glycosylation In
|
|
Carbohydrate-Deficient Glycoprotein Syndromes
|
Cdg Syndrome Type In
|
|
Carbohydrate Deficient Glycoprotein Syndrome Type In
|
Congenital Disorder Of Glycosylation Type 1n
|
|
Man5glcnac2-Pp-Dol Flippase Deficiency
|
Glycosylation, Congenital Disorder Of
|
|
Glycosylation, Congenital Disorder Of, Type In
|
|
|
| Bilirubin Metabolic Disorder |
|
Hyperbilirubinemia
|
Hereditary Hyperbilirubinemia
|
|
Hyperbilirubinemia, Hereditary
|
Hyperbilirubinaemia
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
