Diseases |
Alias |
|
Disseminated Intravascular Coagulation |
Defibrination Syndrome
|
Dic
|
Diffuse Or Disseminated Intravascular Coagulation
|
Fibrinolytic Purpura
|
Consumption Coagulopathy
|
Diffuse Intravascular Coagulation
|
Dic - [Disseminated Intravascular Coagulation]
|
Disseminated Intravascular Coagulopathy
|
Fibrinolysis Nos
|
Thrombolytic Purpura
|
|
|
Complete Plasminogen Activator Inhibitor 1 Deficiency |
Congenital Plasminogen Activator Inhibitor Type 1 Deficiency
|
Complete Pai-1 Deficiency
|
Homozygous Pai-1 Deficiency
|
Hyperfibrinolysis Due To Pai1 Deficiency
|
Pai-1 Deficiency
|
Pai-1d
|
Pai1 Deficiency
|
Plasminogen Activator Inhibitor Type 1 Deficiency
|
Plasminogen Inhibitor-1 Deficiency
|
Quantitative Pai-1 Deficiency
|
Congenital Pai-1 Deficiency
|
Congenital Pai-1 - [Plasminogen Activator Inhibitor Type 1] Deficiency
|
|
|
Peyronie'S Disease |
Induratio Penis Plastica
|
Peyronie Disease
|
Peyronies Disease
|
Peyronie'S Fibromatosis
|
Penile Induration
|
Balanitis Xerotica Obliterans
|
|
|
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
|
|
|
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
|
|
|
Fibrinolytic Defect |
|
|
Dysbaric Osteonecrosis |
Caisson Disease Of Bone
|
Don
|
|
|
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
|
|
|
Ureteral Disease |
Ureteral Diseases
|
Ureteral Disorders
|
Disorder Of Ureter
|
|
|
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
|
|
|
Venous Insufficiency |
Peripheral Venous Insufficiency
|
|
|
Lipid Metabolism Disorder |
Dyslipidemia
|
Disorder Of Fatty Acid Metabolism
|
Lipid Metabolism Disorders
|
Fatty Acid Metabolism Disorder
|
Disorder Of Lipid Metabolism
|
Abnormality Of Lipid Metabolism
|
Lipid Metabolism, Inborn Errors
|
Dyslipidemias
|
Disorders Of Lipid Metabolism
|
Congenital Disorders Of Lipid Metabolism
|
Inherited Disorders Of Lipid Metabolism
|
|
|
Diabetic Angiopathy |
Diabetic Angiopathies
|
Diabetic Peripheral Angiopathy
|
Diabetic Vascular Disorder
|
|
|
Dic In Newborn |
Disseminated Intravascular Coagulation In Newborn
|
|
|
Hyperinsulinism |
|
|
Coronary Thrombosis |
Coronary Artery Thrombosis
|
|
|
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]
|
|
|
Microvascular Complications Of Diabetes 5 |
Diabetic Retinopathy
|
Microvascular Complications Of Diabetes, Susceptibility To, 5
|
MVCD5
|
Retinopathy, Diabetic
|
Diabetic Nephropathy
|
Retinopathy, Diabetic, Susceptibility To
|
Retinal Abnormality - Diabetes-Related
|
|
|
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
|
|
|
Hyperuricemia |
Blood Urate Raized
|
Uricacidemia
|
|
|
Hypertriglyceridemia 1 |
Hypertriglyceridemia
|
Hypertriglyceridemia, Familial
|
Hypertriglyceridemia, Susceptibility To
|
HYTG1
|
FHTR
|
Hypertriglyceridemias Familial
|
|
|
Acquired Metabolic Disease |
|
|
Coronary Stenosis |
|
|
Arteriosclerosis |
Arteriosclerotic Vascular Disease
|
|
|
Intracranial Arteriosclerosis |
|
|
Thrombocytopenia |
Low Platelet Count
|
Low Platelets
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
Yellow Fever |
Urban Yellow Fever
|
Jungle Yellow Fever
|
Sylvatic Yellow Fever
|
Yf
|
Yellow Fever, Sylvan
|
Bronze John
|
Yellow Jack
|
Yf- [Yellow Fever]
|
Febris Flava
|
|
|
Cardiovascular System Disease |
Abnormality Of The Cardiovascular System
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
Cardiovascular Diseases
|
Cardiovascular Disease
|
|
|
Protein C Deficiency |
Hereditary Thrombophilia Due To Protein C Deficiency
|
Proc Deficiency
|
Congenital Thrombotic Disease, Due To Protein C Deficiency
|
|
|
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
|
|
|
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
|
|
|
Retinal Vein Occlusion |
Occlusion, Of Retinal Vein
|
|
|
Autism |
Autistic Disorder
|
Autism Susceptibility 1
|
Childhood Autism
|
Autistic Disorder Of Childhood Onset
|
Infantile Autism
|
Kanner'S Syndrome
|
Autistic
|
|
|
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
|
|
|
Carotid Artery Thrombosis |
|
|
Hypothyroidism |
Thyroid Diseases
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
Dysfunction Thyroid
|
Thyroid Disease
|
Thyroid Dysfunction
|
|
|
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
|
|
|
Post-Thrombotic Syndrome |
Postphlebitic Syndrome
|
Postthrombotic Syndrome
|
Postphlebetic Syndrome With Inflammation
|
Postphlebetic Syndrome With Ulcer
|
Postphlebetic Syndrome With Ulcer And Inflammation
|
Venous Stress Disorder
|
|
|
Body Mass Index Quantitative Trait Locus 11 |
OBESITY
|
Obesity, Susceptibility To
|
Leanness, Inherited
|
Obesity, Susceptibility To, Bmiq11
|
Obesity, Mild, Early-Onset
|
Obesity, Association With
|
Obesity, Early-Onset, Susceptibility To
|
Obesity, Severe
|
Obesity, Severe, And Type Ii Diabetes
|
Obesity, Late-Onset
|
BMIQ11
|
Obesity Bmiq11
|
Obesity, Early-Onset
|
Obesity , Susceptibility To
|
Simple Obesity Nos
|
Excess Fat
|
Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified
|
Adiposis
|
|
|
Breast Cancer |
Breast Carcinoma
|
Breast Cancer, Familial
|
Malignant Neoplasm Of Breast
|
Male Breast Cancer
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
Mammary Cancer
|
Mammary Tumor
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
Familial Breast Cancer
|
Cancer Of Breast
|
BC
|
Breast Cancer Familial
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
Breast Male Carcinoma
|
Breast Neoplasms
|
Breast Neoplasms, Male
|
Mammary Tumors
|
Mammary Carcinomas
|
Cancer, Breast
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
Carcinoma With Apocrine Differentiation
|
|
|
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
|
|
|
Intermittent Claudication |
Charcot'S Syndrome
|
Amyotrophic Lateral Sclerosis
|
|
|
Thrombosis |
Thrombosis Of Blood Vessel
|
|
|
Aortic Aneurysm |
Aortic Rupture
|
Thoracoabdominal Aortic Aneurysm, Ruptured
|
Ruptured Aortic Aneurysm
|
Aortic Aneurysms
|
Aortic Aneurysm Without Mention Of Rupture Nos
|
Ruptured Abdominal Aortic Aneurysm
|
Aortic Aneurysm, Ruptured
|
Ruptured Thoracic Aortic Aneurysm
|
|
|
Trochlear Nerve Disease |
Trochlear Nerve Diseases
|
Disorder Of Trochlear Nerve
|
Superior Oblique Muscle Innervation Disorder
|
Trochlear Nerve Disorder
|
Fourth Cranial Nerve Paresis
|
|
|
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
|
|
|
Lipoprotein Quantitative Trait Locus |
Coronary Artery Disease
|
Coronary Artery Disease, Susceptibility To
|
Coronary Artery Anomaly
|
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
|
|
|
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
|
|
|
Renal Fibrosis |
|
|
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
|
|
|
Thrombophilia |
|
|
Prostate Cancer |
Prostate Carcinoma
|
Prostate Cancer, Familial
|
Prostate Neoplasm
|
Prostate Cancer, Somatic
|
Prostate Cancer, Susceptibility To
|
Prostatic Cancer
|
Prostatic Neoplasms
|
Hereditary Prostate Cancer
|
Prostatic Neoplasm
|
Cancer Of Prostate
|
Carcinoma Of Prostate
|
Familial Prostate Cancer
|
Familial Prostate Carcinoma
|
Malignant Tumor Of Prostate
|
Malignant Neoplasm Of Prostate
|
Prostate Cancer, Familial, Susceptibility To
|
Malignant Tumor Of The Prostate
|
Ngp - New Growth Of Prostate
|
Tumor Of The Prostate
|
Prostate Cancer, Hereditary
|
Cancer Of The Prostate
|
Malignant Neoplasm Of The Prostate
|
Prostatic Carcinoma
|
PC
|
Prca
|
Cancer, Prostate
|
Malignant Prostatic Tumour
|
Malignant Tumour Of Prostate
|
Primary Prostate Cancer
|
Primary Malignant Neoplasm Of Prostate
|
Prostate Gland Cancer
|
|
|
Medulloadrenal Hyperfunction |
|
|
Obstructive Nephropathy |
Con
|
Congenital Obstructive Nephropathy
|
Nephropathy Obstructive
|
|
|
Malignant Secondary Hypertension |
|
|
Fibrosarcoma |
Neoplasms, Fibrous Tissue
|
Fibrocytic Tumor
|
Fibrosarcoma Of Soft Tissue
|
Fibrous Tissue Neoplasm
|
|
|
Pneumoconiosis |
Pneumoconioses
|
Silicosis Nos
|
Complicated Silicosis
|
Fibrosis Of Lung With Silicosis
|
Nodular Silicosis
|
Pneumoconiosis Due To Silica
|
Silicotic Fibrosis Of Lung
|
Simple Silicosis
|
Silicatosis
|
Silicotic Lung Fibrosis
|
Pneumoconiosis Due To Talc
|
Pulmonary Talcosis
|
Talc Lung Disease
|
Talc Pneumoconiosis
|
Talc Workers' Pneumoconiosis
|
Talcosis
|
Fibrosis Of Lung Due To Talc
|
Asbestos Pneumoconiosis
|
Amianthosis
|
Asbestosis
|
Lung Fibrosis With Asbestosis
|
Pulmonary Asbestosis
|
|
|
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
|
|
|
Malignant Renovascular Hypertension |
Secondary Malignant Renovascular Hypertension
|
|
|
Central Serous Chorioretinopathy |
Central Serous Chorioretinopathy After Bone Marrow Transplantation
|
Central Serous Choroidopathy
|
Cscr
|
Central Serous Retinopathy
|
Central Serous Choroidoretinopathy
|
|
|
Legg-Calve-Perthes Disease |
Perthes Disease
|
LCPD
|
Coxa Plana
|
Legg-Perthes Disease
|
Juvenile Osteochondrosis Of Hip And Pelvis
|
Pseudocoxalgia
|
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
|
Legg-Calvé-Perthes Disease
|
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
|
|
|
Premature Ovarian Failure 19 |
POF19
|
Primary Ovarian Insufficiency 19
|
Poi19
|
Ovarian Failure, Premature, Type 19
|
|
|
Thrombophilia Due To Activated Protein C Resistance |
Activated Protein C Resistance
|
Apc Resistance
|
THPH2
|
Thrombophilia Due To Deficiency Of Activated Protein C Cofactor
|
Proc Cofactor Deficiency
|
Pccf Deficiency
|
Thrombophilia V
|
Thrombophilia, Susceptibility To, Due To Factor V Leiden
|
Thrombophilia Due To Factor V Leiden
|
Thrombophilia 2 Due To Activated Protein C Resistance
|
Thrombophilia, Susceptibility To, Due To Activated Protein C Resistance
|
|
|
Pulmonary Embolism |
Pulmonary Artery Embolism
|
Pulmonary Embolus
|
Pulmonary Emboli
|
|
|
Hyperhomocysteinemia |
|
|
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
|
|
|
Coronary Heart Disease 1 |
Coronary Heart Disease
|
Coronary Heart Disease, Susceptibility To, 1
|
Chds1
|
Coronary Heart Disease, Susceptibility To
|
CHD
|
Heart, Coronary, Disease, Susceptibility To, Type 1
|
Coronary Arteriosclerosis
|
Coronary Artery Disease
|
|
|
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
|
|
|
Placenta Accreta |
|
|
Aortic Aneurysm, Familial Abdominal, 1 |
Abdominal Aortic Aneurysm
|
Aortic Aneurysm, Familial Abdominal 1
|
Aneurysm, Abdominal Aortic
|
AAA
|
Aortic Aneurysm, Abdominal
|
AAA1
|
Aortic Aneurysm, Familial Abdominal
|
Aortic Aneurysm Abdominal
|
Abdominal Aortic Aneurysms
|
Abdominal Aortic Aneurysm Without Mention Of Perforation Or Rupture
|
Abdomen Aneurysm
|
Abdominal Aorta Aneurysm
|
Aneurysm Of Abdominal Aorta
|
Aortic Abdomen Aneurysm
|
Aaa - [Abdominal Aortic Aneurysm]
|
Abdominal Aneurysm
|
Abdominal Aorta Aneurysm Rupture
|
Abdominal Aorta Aneurysm Ruptured
|
Abdominal Aortic Aneurysm Which Has Ruptured
|
Ruptured Aaa
|
Abdomen Aorta Aneurysm Ruptured
|
Abdomen Aorta Rupture
|
Abdomen Aortic Aneurysm Rupture
|
Abdomen Aneurysm Rupture
|
Abdomen Aortic Aneurysm Ruptured
|
Abdomen Aortic Rupture
|
Abdominal Aorta Rupture
|
Abdominal Aortic Rupture
|
Rupture Abdomen Aorta Aneurysm
|
Rupture Abdominal Aortic Aneurysm
|
Ruptured Abdomen Aneurysm
|
Ruptured Abdomen Aorta
|
Ruptured Abdomen Aortic
|
Ruptured Abdominal Aneurysm
|
Ruptured Abdominal Aorta
|
Ruptured Abdominal Aortic
|
Ruptured Aorta Abdominalis Aneurysm
|
False Abdomen Aorta Aneurysm Ruptured
|
False Abdominal Aortic Aneurysm Ruptured
|
False Abdominal Aorta Aneurysm Ruptured
|
False Abdomen Aortic Aneurysm Ruptured
|
|
|
Diabetes Mellitus |
|
|
Chronic Venous Insufficiency |
|
|
Respiratory Failure |
Acute Respiratory Failure
|
Chronic Respiratory Failure
|
Respiratory Insufficiency
|
Acute-On-Chronic Respiratory Failure
|
Acute And Chronic Respiratory Failure
|
Respiratory Insufficiency/Failure
|
Chronic Respiratory Disease
|
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
|
|
|
Sleep Apnea |
|
|
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
|
|
|
Protein S Deficiency |
Protein S Deficiency Disease
|
Hereditary Thrombophilia Due To Protein S Deficiency
|
|
|
Type 2 Diabetes Mellitus |
Insulin Resistance
|
NIDDM
|
Diabetes Mellitus, Non-Insulin-Dependent
|
Type 2 Diabetes
|
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
|
|
|
Alpha-1-Antitrypsin Deficiency |
Alpha 1-Antitrypsin Deficiency
|
Alpha-1 Antitrypsin Deficiency
|
Aat Deficiency
|
Aatd
|
A1ATD
|
Emphysema Due To Aat Deficiency
|
A1at Deficiency
|
Hemorrhagic Diathesis Due To Antithrombin Pittsburgh
|
Emphysema-Cirrhosis, Due To Aat Deficiency
|
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
|
|
|
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
|
|
|
Amaurosis Fugax |
Transient Monocular Blindness
|
Momentary Blindness
|
Af - [Amaurosis Fugax]
|
Transient Vision Loss, Spontaneous
|
Amaurosis Fugax, Course Of Resolution Unspecified
|
|
|
Subendocardial Myocardial Infarction |
|
|
Urinary Tract Obstruction |
Obstructive Uropathy
|
Urinary Obstruction
|
Urologic Diseases
|
|
|
Prediabetes Syndrome |
Impaired Glucose Tolerance
|
Prediabetes
|
Prediabetic State
|
IGT
|
Igt - [Impaired Glucose Tolerance]
|
Impaired Glucose Tolerance With Unspecified Complication
|
Impaired Glucose Tolerance Without Complication
|
Abnormal Glucose Tolerance
|
|
|
Plasminogen Activator Inhibitor-1 Deficiency |
Hyperfibrinolysis Due To Pai1 Deficiency
|
Plasminogen Activator Inhibitor Type 1 Deficiency
|
Pai-1 Deficiency
|
Pai1 Deficiency
|
Plasminogen Activator Inhibitor 1 Deficiency
|
PAI-1D
|
Plasminogen Activator Inhibitor, Type I
|
Deficiency, Plasminogen Activator Inhibitor-1
|
|
|
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
|
|
|
Vascular Disease |
Vascular Diseases
|
Aneurysm
|
Spinal Cord Ischemia
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
Vascular Anomaly
|
|
|
Abdominal Obesity-Metabolic Syndrome 1 |
Metabolic Syndrome X
|
Metabolic Syndrome
|
AOMS1
|
Dysmetabolic Syndrome X
|
Metabolic Disease
|
Abdominal Obesity Metabolic Syndrome
|
|
|
Afibrinogenemia, Congenital |
Congenital Afibrinogenemia
|
Afibrinogenemia
|
Factor I Deficiency
|
Familial Afibrinogenemia
|
Hypofibrinogenemia, Congenital
|
Fibrinogen Deficiency
|
Afibrinogenemia Congenital
|
CAFBN
|
Congenital Hypofibrinogenemia
|
Hypofibrinogenemia
|
Complement Factor I Deficiency
|
|
|
Non-Alcoholic Fatty Liver Disease |
Fatty Liver
|
Non-Alcoholic Fatty Liver
|
Nafld
|
Nonalcoholic Fatty Liver Disease
|
Nonalcoholic Steatohepatitis
|
Steatosis
|
Nafl
|
Nash
|
Non-Alcoholic Steatohepatitis
|
Susceptibility To Nonalcoholic Fatty Liver Disease
|
Steatohepatitis
|
Fatty Degeneration
|
Non-Alcoholic Fatty Liver Disease Without Mention Of Non-Alcoholic Steatohepatitis
|
Nafld Without Nash
|
Nafld Without Mention Of Nash
|
|
|
Pulmonary Artery Disease |
Abnormality Of The Pulmonary Artery
|
|
|
Arthrogryposis, Distal, Type 2b2 |
DA2B2
|
Distal Arthrogryposis Type 2b2
|
Arthrogryposis, Distal, 2b2
|
|
|
Atherosclerosis Susceptibility |
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
Alp
|
Arteriosclerosis
|
|
|
Familial Hyperlipidemia |
Familial Hyperlipoproteinemia
|
Hyperlipidaemia
|
Hyperlipoproteinemias
|
Hyperlipemia
|
Hyperlipidemias
|
Hyperlipidemia
|
|
|
Vein Disease |
|
|
Hyperglycemia |
|
|
Peripheral Vascular Disease |
Peripheral Arterial Disease
|
Arterial Occlusive Disease
|
Arterial Occlusive Diseases
|
Pad
|
Peripheral Vascular Diseases
|
Peripheral Occlusive Disease
|
Peripheral Arterial Diseases
|
Helicobacter Infections
|
|
|
Hepatic 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
|
|
|
Endocarditis |
|
|
Cerebral Palsy |
Infantile Cerebral Palsy
|
Mixed Cerebral Palsy
|
Palsy Cerebral
|
Palsy, Cerebral
|
Cerebral Palsy, Mixed
|
|
|
Nervous System Disease |
Abnormality Of The Nervous System
|
Nervous System Diseases
|
Nervous System Disorder
|
|
|
Arthrogryposis, Distal, Type 2b1 |
Sheldon-Hall Syndrome
|
Freeman-Sheldon Syndrome Variant
|
Distal Arthrogryposis Type 2b1
|
DA2B1
|
Arthrogryposis Multiplex Congenita, Distal, Type 2b
|
Shs
|
Distal Arthrogryposis Type 2b
|
Fssv
|
Arthrogryposis Multiplex Congenita Distal Type 2b
|
Arthrogryposis Multiplex Congenita Distal Type Ii With Craniofacial Abnormalities
|
Da2b
|
Arthrogryposis Multiplex Congenita, Distal, Type Ii, With Craniofacial Abnormalities
|
Distal Arthrogryposis Type Iib
|
Freeman Sheldon Syndrome, Variant
|
Freeman Sheldon Variant
|
Arthrogryposis, Distal, 2b1
|
Amcd2b
|
|
|
Interstitial Lung Disease 2 |
Idiopathic Pulmonary Fibrosis
|
Ipf
|
Fibrocystic Pulmonary Dysplasia
|
Pulmonary Fibrosis, Idiopathic
|
Pulmonary Fibrosis, Idiopathic, Susceptibility To
|
ILD2
|
Idiopathic Pulmonary Fibrosis, Familial
|
Fibrosing Alveolitis, Cryptogenic
|
Uip
|
Cryptogenic Fibrosing Alveolitis
|
Fibrosing Alveolitis
|
Interstitial Pneumonitis, Usual
|
Familial Idiopathic Pulmonary Fibrosis
|
Idiopathic Fibrosing Alveolitis, Chronic Form
|
Usual Interstitial Pneumonia
|
Fibrosing Alveolitis Cryptogenic
|
Hamman-Rich Disease
|
Idiopathic Pulmonary Fibrosis Familial
|
Interstitial Pneumonitis Usual
|
Fibrosis Idiopathic Pulmonary
|
Fibrosis, Pulmonary, Idiopathic
|
Hamman-Rich Syndrome
|
Chronic Idiopathic Pulmonary Fibrosis
|
Acute Interstitial Pneumonia
|
Interstitial Pulmonary Fibrosis
|
Ipf - [Idiopathic Pulmonary Fibrosis]
|
Idiopathic Lung Fibrosis
|
Fibrosing Lung Disease
|
Pulmonary Fibrosis Nos
|
Fibrosing Pneumonitis
|
|
|
Acute Myocardial Infarction |
Cardiac Attack
|
Heart Attack
|
|
|
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
|
|
|
Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 |
Abdominal Obesity-Metabolic Syndrome
|
Abdominal Obesity Metabolic Syndrome
|
Metabolic Syndrome X
|
Aoms2
|
Aoms1
|
|
|
Pseudoxanthoma Elasticum |
PXE
|
Gronblad-Strandberg Syndrome
|
Pseudoxanthoma Elasticum, Modifier Of Severity Of
|
Gronblad-Strandberg-Touraine Syndrome
|
Gronblad Strandberg Syndrome
|
Groenblad-Strandberg Syndrome
|
Nevus Elasticus
|
Pxe - [Pseudoxanthoma Elasticum]
|
|
|
Aortic Aneurysm, Familial Thoracic 1 |
Thoracic Aortic Aneurysm
|
Annuloaortic Ectasia
|
Familial Thoracic Aortic Aneurysm And Aortic Dissection
|
Familial Aortic Dissection
|
Familial Taad
|
Congenital Aneurysm Of Ascending Aorta
|
Familial Aortic Aneurysm
|
Familial Thoracic Aortic Aneurysm
|
Familial Thoracic Aortic Aneurysm And Dissection
|
Aortic Aneurysm, Thoracic
|
AAT1
|
Faa1
|
Aortic Dissection, Familial
|
Aortic Aneurysm, Familial Thoracic
|
Aneurysm, Thoracic Aortic
|
Faa
|
Ftaad
|
Taa
|
Taad
|
Cystic Medial Necrosis Of Aorta
|
Familial Non-Syndromic Thoracic Aortic Aneurysm And Aortic Dissection
|
Aortic Aneurysm Thoracic
|
Familial Aortic Aneurysms
|
Aneurysm, Aortic, Thoracic, Familial, Type 1
|
Aneurysm Of Thoracic Aorta
|
Intrathoracic Aneurysm
|
Thoracic Aorta Aneurysm
|
Thoracic Aortic Aneurysm Without Rupture
|
Thoracic Aneurysm
|
Thorax Arterial Aneurysm
|
Thoracic Artery Aneurysm
|
Thoracic Arterial Aneurysm
|
Thorax Aneurysm
|
Thorax Aortic Aneurysm
|
Dissection Of Thoracic Aorta
|
|
|
Hepatic Vascular Disease |
Vascular Disorder Of Liver
|
|
|
Placental Insufficiency |
Uteroplacental Vascular Insufficiency
|
|
|
Retinal Artery Occlusion |
Retina Artery Narrowing
|
Retinal Artery Spasm
|
Spasm Of Ophthalmic Artery
|
Retinal Spasm
|
Vasospasm Of Retina
|
|
|
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]
|
|
|
Autism Spectrum Disorder |
Asd
|
Autism Spectrum Disorders
|
Autistic Continuum
|
Pervasive Developmental Disorder
|
Pervasive Development Disorder
|
Autistic Behavior
|
Autistic Disorder
|
Autistic
|
Autistic Disorder Of Childhood Onset
|
Infantile Autism
|
Childhood Autism
|
Kanner Syndrome
|
Pervasive Developmental Delay Nos
|
Pervasive Developmental Disorder, Not Otherwise Specified
|
|
|
Polycystic Ovary Syndrome |
Polycystic Ovarian Syndrome
|
Pcos
|
Polycystic Ovaries
|
Stein-Leventhal Syndrome
|
Multicystic Ovaries
|
Polycystic Ovarian Disease
|
Polycystic Ovary
|
Sclerocystic Ovaries
|
Sclerocystic Ovary Syndrome
|
Stein-Leventhal Synd.
|
Cystic Disease Of Ovaries
|
Cystic Disease Of Ovary
|
Pco
|
Pcod
|
Sclerocystic Ovarian Degeneration
|
Polycystic Ovary Syndrome, Susceptibility To
|
Pcos - [Polycystic Ovary Syndrome]
|
Polycystic Ovary Nos
|
Pco - [Polycystic Ovary]
|
|
|
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
|
|
|
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
|
|
|
Pulmonary Fibrosis |
|
|
Advanced Sleep Phase Syndrome, Familial, 1 |
Advanced Sleep Phase Syndrome 1
|
FASPS1
|
Familial Advanced Sleep Phase Syndrome 1
|
Sleep Phase Syndrome, Advanced, Familial, Type 1
|
|
|
Overnutrition |
|
|
Heart Disease |
Heart Failure
|
Congenital Heart Disease
|
Heart Diseases
|
Congenital Heart Defects
|
Congenital Heart Defect
|
Congenital Anomaly Of Heart
|
Heart Defect
|
Heart Malformation
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
Heart Defects
|
Heart Disease, Congenital
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|