Medical specialists from Belgium tagged by Regulatory Authorities as investigators in clinical studies for the listed conditions:
A
-
Abdominal Aortic Aneurysm
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Abortion, Spontaneous
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Acidosis
-
Acidosis, Renal Tubular
-
Acquired Immunodeficiency Syndrome
-
Acute Coronary Syndrome
-
Acute Lymphoblastic Leukemia
-
Acute Myeloid Leukemia
-
Acute Non Lymphoblastic Leukemia
-
Acute Pain
-
Acute Respiratory Distress Syndrome
-
Adenocarcinoma
-
Adenocarcinoma, Bronchiolo-Alveolar
-
Adenomatous Polyps
-
Adenosarcoma
-
Adrenal Hyperplasia, Congenital
-
Adrenogenital Syndrome
-
Adrenoleukodystrophy
-
Adrenomyeloneuropathy
-
Adult Neuronal Ceroid Lipofuscinosis
-
Alagille Syndrome
-
Alcohol Drinking
-
Alcoholism
-
Allergic Angiitis
-
Alpha 1-Antitrypsin Deficiency
-
Alpha-1 Antitrypsin Deficiency
-
Alpha-thalassemia
-
Alport Syndrome
-
Alzheimer Disease
-
Amyloid Neuropathies
-
Amyloid Neuropathy
-
Amyloidosis
-
Amyotrophic Lateral Sclerosis
-
Andersen Syndrome
-
Andersen-Tawil Syndrome
-
Anemia
-
Anemia, Diamond-Blackfan
-
Anemia, Megaloblastic
-
Anemia, Refractory, with Excess of Blasts
-
Anemia, Sickle Cell
-
Aneurysm
-
Aneurysm, Dissecting
-
Aneurysm, Ruptured
-
Angelman Syndrome
-
Angina Pectoris
-
Angina Pectoris, Variant
-
Angina, Stable
-
Ankle Injuries
-
Anorchia
-
Anorexia
-
Anorexia Nervosa
-
Anxiety Disorders
-
Aortic Aneurysm
-
Aortic Aneurysm, Abdominal
-
Aortic Arch Syndromes
-
Aortic Diseases
-
Aortic Root Aneurysm
-
Aortic Valve Disease
-
Aortic Valve Insufficiency
-
Aortic Valve Stenosis
-
Aphasia, Primary Progressive
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Apnea
-
Arachnodactyly
-
Argininosuccinic Aciduria
-
Aromatic L-amino Acid Decarboxylase Deficiency
-
Arrhythmias, Cardiac
-
Arteriovenous Fistula
-
Arteriovenous Malformations
-
Arteritis
-
Arthritis
-
Arthritis, Juvenile
-
Arthritis, Psoriatic
-
Arthritis, Rheumatoid
-
Arthrogryposis
-
Aspergillosis
-
Asthenia
-
Asthma
-
Astigmatism
-
Ataxia
-
Ataxia With Vitamin E Deficiency
-
Atherosclerosis
-
Athletic Injuries
-
Atrial Fibrillation
-
Atrial Flutter
-
Atrioventricular Block
-
Atrophy
-
Attention Deficit Disorder with Hyperactivity
-
Autism Spectrum Disorder
-
Autistic Disorder
-
Autoimmune Diseases
-
Autonomic Nervous System Diseases
-
Autosomal Dominant Multiple Pterygium Syndrome
-
alpha-Thalassemia
B
-
B-cell Lymphoma
-
Back Pain
-
Bacteremia
-
Barrett Esophagus
-
Becker Muscular Dystrophy
-
Behavior, Addictive
-
Beta Ketothiolase Deficiency
-
Bilateral Vestibulopathy
-
Bile Reflux
-
Biliary Tract Cancer
-
Biliary Tract Neoplasms
-
Biotin-thiamine-responsive Basal Ganglia Disease
-
Biotinidase Deficiency
-
Blind Loop Syndrome
-
Blindness
-
Blood Coagulation Disorders
-
Blood Loss, Surgical
-
Body Odor
-
Body Weight
-
Bone Marrow Diseases
-
Bone Neoplasms
-
Brachial Plexus Neuritis
-
Bradycardia
-
Brain Diseases
-
Brain Dopamine-serotonin Vesicular Transport Disease
-
Brain Edema
-
Brain Injuries
-
Brain Injuries, Traumatic
-
Brain Neoplasms
-
Breast Cancer Lymphedema
-
Breast Neoplasms
-
Bronchiolitis
-
Bronchopulmonary Dysplasia
-
Brugada Syndrome
-
Bursitis
C
-
CDKL5 Deficiency Disorder
-
COVID-19
-
Cachexia
-
Calcinosis
-
Cancer Pain
-
Candidemia
-
Candidiasis
-
Candidiasis, Invasive
-
Carbamoyl-Phosphate Synthase I Deficiency Disease
-
Carcinoid Tumor
-
Carcinoma
-
Carcinoma, Basal Cell
-
Carcinoma, Hepatocellular
-
Carcinoma, Lobular
-
Carcinoma, Merkel Cell
-
Carcinoma, Neuroendocrine
-
Carcinoma, Non-Small-Cell Lung
-
Carcinoma, Ovarian Epithelial
-
Carcinoma, Renal Cell
-
Carcinoma, Squamous Cell
-
Carcinoma, Transitional Cell
-
Cardiomyopathies
-
Cardiomyopathy, Dilated
-
Cardiomyopathy, Hypertrophic
-
Cardiomyopathy, Hypertrophic, Familial
-
Cardiospasm
-
Cardiotoxicity
-
Caregiver Burden
-
Carnitine Palmitoyl Transferase 1A Deficiency
-
Carnitine-acylcarnitine Translocase Deficiency
-
Carotid Artery Injuries
-
Carotid Stenosis
-
Carpal Tunnel Syndrome
-
Cataract
-
Catecholaminergic Polymorphic Ventricular Tachycardia
-
Celiac Disease
-
Central Nervous System Diseases
-
Central Nervous System Neoplasms
-
Cerebellar Ataxia
-
Cerebral Folate Deficiency
-
Cerebral Hemorrhage
-
Cerebral Infarction
-
Cerebral Palsy
-
Channelopathies
-
Charcot-Marie-Tooth Disease
-
Chediak-Higashi Syndrome
-
Chemotherapy-Induced Febrile Neutropenia
-
Child Development Disorders, Pervasive
-
Childhood Acute Lymphoblastic Leukemia
-
Childhood Encephalopathy Due to Thiamine Pyrophosphokinase Deficiency
-
Cholangiocarcinoma
-
Cholangitis
-
Cholangitis, Sclerosing
-
Cholecystitis
-
Cholestasis
-
Cholestasis, Intrahepatic
-
Cholesteryl Ester Storage Disease
-
Chronic Disease
-
Chronic Graft Versus Host Disease
-
Chronic Granulomatous Disease
-
Chronic Lymphocytic Leukemia
-
Chronic Myeloid Leukemia
-
Chronic Myeloproliferative Disorders
-
Chronic Pain
-
Chronic Periodontitis
-
Chronic Thromboembolic Pulmonary Hypertension
-
Churg-Strauss Syndrome
-
Ciliary Motility Disorders
-
Citrullinemia
-
Citrullinemia Type II
-
Cleft Palate
-
Cocaine-Related Disorders
-
Cognition Disorders
-
Cognitive Dysfunction
-
Colitis
-
Colitis, Ulcerative
-
Colonic Neoplasms
-
Colorectal Neoplasms
-
Communicable Diseases
-
Compulsive Personality Disorder
-
Congenital Abnormalities
-
Congenital Adrenal Hyperplasia
-
Congenital Hyperinsulinism
-
Congenital Hypothyroidism
-
Congenital Myasthenic Syndromes
-
Congenital Sucrase-isomaltase Deficiency
-
Connective Tissue Diseases
-
Consciousness Disorders
-
Constipation
-
Constriction, Pathologic
-
Corneal Edema
-
Corneal Endothelial Cell Loss
-
Coronary Artery Disease
-
Coronary Disease
-
Coronary Occlusion
-
Coronary Restenosis
-
Coronary Stenosis
-
Coronary Vasospasm
-
Coronavirus Infections
-
Crigler Najjar Syndrome, Type 1
-
Crigler-Najjar Syndrome
-
Critical Illness
-
Crohn Disease
-
Cryptorchidism
-
Cumulative Trauma Disorders
-
Cystadenocarcinoma, Serous
-
Cystic Fibrosis
-
Cystinosis
-
Cystinuria
-
Cytomegalic Inclusion Disease
-
Cytomegalovirus Infections
D
-
Deafness
-
Death
-
Deglutition Disorders
-
Dementia
-
Depression
-
Depression, Postpartum
-
Depressive Disorder
-
Depressive Disorder, Major
-
Depressive Disorder, Treatment-Resistant
-
Dermatitis
-
Dermatitis, Atopic
-
Desmoplastic Small Round Cell Tumor
-
Developmental Disabilities
-
Developmental Dysphasia Familial
-
Diabetes Insipidus
-
Diabetes Insipidus, Nephrogenic
-
Diabetes Mellitus
-
Diabetes Mellitus, Type 1
-
Diabetes Mellitus, Type 2
-
Diabetes, Gestational
-
Diabetic Foot
-
Diabetic Ketoacidosis
-
Diabetic Nephropathies
-
Diabetic Retinopathy
-
Diamond-Blackfan Anemia
-
Diastasis, Muscle
-
Diffuse Large B-Cell Lymphoma
-
Digestive System Diseases
-
Dilatation, Pathologic
-
Dilated Cardiomyopathy
-
Disease Progression
-
Dissection, Ascending Aorta
-
Diurnal Enuresis
-
Diverticular Diseases
-
Diverticulitis
-
Diverticulum
-
Dopamine Beta Hydroxylase Deficiency
-
Down Syndrome
-
Dravet Syndrome
-
Drug Resistant Epilepsy
-
Drug-Related Side Effects and Adverse Reactions
-
Duchenne Muscular Dystrophy
-
Ductus Arteriosus, Patent
-
Dumping Syndrome
-
Dupuytren Contracture
-
Dyskinesias
-
Dyslipidemias
-
Dyspepsia
-
Dysphonia
-
Dyspnea
-
Dyssomnias
E
-
Eclampsia
-
Eczema
-
Edema
-
Egg Hypersensitivity
-
Embolism
-
Emergencies
-
Emphysema
-
Empyema
-
Empyema, Pleural
-
Endocarditis
-
Endocarditis, Bacterial
-
Endometrial Neoplasms
-
Endometrial Stromal Sarcoma
-
Endometriosis
-
Enthesitis-related Juvenile Idiopathic Arthritis
-
Enthesopathy
-
Enuresis
-
Eosinophilic Esophagitis
-
Eosinophilic Gastroenteritis
-
Eosinophilic Granulomatosis With Polyangiitis
-
Ependymoma
-
Epilepsies, Myoclonic
-
Epilepsy
-
Epstein-Barr Virus Infections
-
Erectile Dysfunction
-
Escherichia coli Infections
-
Esophageal Achalasia
-
Esophageal Cancer
-
Esophageal Neoplasms
-
Esophageal Squamous Cell Carcinoma
-
Esophageal Stenosis
-
Esophagitis
-
Esophagitis, Peptic
-
Essential Thrombocythemia
-
Ewing Sarcoma
-
Eye Abnormalities
-
Eye Diseases
F
-
Failure to Thrive
-
Fallopian Tube Cancer
-
Fallopian Tube Neoplasms
-
Familial Alzheimer Disease
-
Familial Chylomicronemia Syndrome
-
Familial Hemophagocytic Lymphohistiocytosis
-
Familial Hypertrophic Cardiomyopathy
-
Familial Hypophosphatemic Rickets
-
Familial Lipoprotein Lipase Deficiency
-
Familial Primary Pulmonary Hypertension
-
Familial Transthyretin Amyloidosis
-
Fanconi Anemia
-
Fanconi Bickel Syndrome
-
Fanconi Syndrome
-
Fasciitis
-
Fasciitis, Necrotizing
-
Fatigue
-
Fatigue Syndrome, Chronic
-
Fatty Liver
-
Febrile Neutropenia
-
Fecal Incontinence
-
Femoracetabular Impingement
-
Femoral Fractures
-
Fever
-
Fibromyalgia
-
Fibrosis
-
Fistula
-
Follicular Lymphoma
-
Foot Ulcer
-
Fractures, Bone
-
Frailty
-
Friedreich Ataxia
-
Frontotemporal Dementia
-
Frontotemporal Dementia, Ubiquitin-positive
-
Fructose-1,6-Diphosphatase Deficiency
-
Fructose-1,6-bisphosphatase Deficiency
-
Fuchs' Endothelial Dystrophy
G
-
Gait Disorders, Neurologic
-
Galactosemia
-
Galactosemias
-
Gastric Outlet Obstruction
-
Gastro-enteropancreatic Neuroendocrine Tumor
-
Gastroesophageal Reflux
-
Gastrointestinal Diseases
-
Gastrointestinal Hemorrhage
-
Gastrointestinal Neoplasms
-
Gastroparesis
-
Gaucher Disease
-
Gender Dysphoria
-
Genetic Diseases, Inborn
-
Gestational Weight Gain
-
Giant Cell Arteritis
-
Gingivitis
-
Glaucoma
-
Glaucoma, Open-Angle
-
Glioblastoma
-
Glioma
-
Glucose Intolerance
-
Glucose Transporter Type 1 Deficiency Syndrome
-
Glucose-6-phosphate Dehydrogenase Deficiency
-
Glucose-galactose Malabsorption
-
Glucosephosphate Dehydrogenase Deficiency
-
Glutaric Acidemia Type I
-
Glycine Encephalopathy
-
Glycogen Storage Disease
-
Glycogen Storage Disease Type 1A
-
Glycogen Storage Disease Type I
-
Glycogen Storage Disease Type II
-
Graft vs Host Disease
-
Granulocytopenia
-
Granulomatosis With Polyangiitis
-
Granulomatosis with Polyangiitis
-
Granulomatous Disease, Chronic
-
Granulosa Cell Tumor
-
Griscelli Syndrome
H
-
HIV Infections
-
HIV Seropositivity
-
HMG CoA Lyase Deficiency
-
Halitosis
-
Hallux Valgus
-
Hand-Foot Syndrome
-
Head and Neck Neoplasms
-
Hearing Loss
-
Hearing Loss, Bilateral
-
Hearing Loss, Noise-Induced
-
Hearing Loss, Sensorineural
-
Heart Arrest
-
Heart Defects, Congenital
-
Heart Diseases
-
Heart Failure
-
Heart Failure, Diastolic
-
Heart Valve Diseases
-
Heartburn
-
Hemiplegia
-
Hemochromatosis
-
Hemochromatosis Type 3
-
Hemophilia
-
Hemophilia A
-
Hemophilia B
-
Hemorrhage
-
Hemosiderosis
-
Hemostatic Disorders
-
Hepatitis
-
Hepatitis A
-
Hepatitis B
-
Hepatitis B, Chronic
-
Hepatitis C
-
Hepatitis D
-
Hepatitis, Chronic
-
Hepatoblastoma
-
Hepatolenticular Degeneration
-
Hereditary Hyperekplexia
-
Hereditary Motor and Sensory Neuropathy
-
Hereditary Neuropathy With Liability to Pressure Palsies
-
Hereditary Sensory and Motor Neuropathy
-
Hernia
-
Hernia, Femoral
-
Hernia, Inguinal
-
Hernia, Umbilical
-
Hernia, Ventral
-
Herpes Genitalis
-
Herpes Simplex
-
Herpesviridae Infections
-
Hip Fractures
-
Hirschsprung Disease
-
Hoarseness
-
Hodgkin Disease
-
Hodgkin Lymphoma
-
Holocarboxylase Synthetase Deficiency
-
Homocystinuria
-
Homologous Wasting Disease
-
Huntington Disease
-
Hyperammonemia
-
Hypercalciuria
-
Hyperekplexia
-
Hyperglycemia
-
Hyperglycinemia, Nonketotic
-
Hyperkinesis
-
Hyperlipoproteinemia Type I
-
Hyperoxaluria, Primary
-
Hyperplasia
-
Hypersensitivity
-
Hypertension
-
Hypertension, Pregnancy-Induced
-
Hypertension, Pulmonary
-
Hyperthermia
-
Hypertrophy
-
Hyperventilation
-
Hypocalcemia
-
Hypoglycemia
-
Hypoparathyroidism
-
Hypophosphatasia
-
Hypophosphatemia
-
Hypothyroidism
-
Hypoxia
I
-
Idiopathic Achalasia
-
Idiopathic Inflammatory Myopathy
-
Idiopathic Pulmonary Fibrosis
-
Ileus
-
Immunologic Deficiency Syndromes
-
Inclusion Body Myositis
-
Infant, Premature, Diseases
-
Infantile Neuronal Ceroid Lipofuscinosis
-
Infarction
-
Infections
-
Infective Endocarditis
-
Infertility
-
Infertility, Female
-
Infertility, Male
-
Inflammation
-
Inflammatory Bowel Diseases
-
Inflammatory Breast Cancer
-
Inflammatory Breast Neoplasms
-
Influenza, Human
-
Insulin Resistance
-
Intestinal Diseases
-
Intestinal Neoplasms
-
Intracranial Aneurysm
-
Intracranial Arteriovenous Malformations
-
Intracranial Hemorrhages
-
Invasive Fungal Infections
-
Irritable Bowel Syndrome
-
Ischemia
-
Ischemic Attack, Transient
-
Ischemic Stroke
-
Isovaleric Acidemia
J
L
-
LCHAD Deficiency
-
Lambert Eaton Myasthenic Syndrome
-
Lambert-Eaton Myasthenic Syndrome
-
Language Development Disorders
-
Language Disorders
-
Late Onset Disorders
-
Leber Congenital Amaurosis
-
Leber Congenital Amaurosis 10
-
Leg Ulcer
-
Leiomyoma
-
Leiomyosarcoma
-
Lennox Gastaut Syndrome
-
Lennox-Gastaut Syndrome
-
Leukemia
-
Leukemia, B-Cell
-
Leukemia, Lymphocytic, Chronic, B-Cell
-
Leukemia, Lymphoid
-
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
-
Leukemia, Myeloid
-
Leukemia, Myeloid, Acute
-
Leukemia, T-Cell
-
Leukodystrophy
-
Leukodystrophy, Metachromatic
-
Lewy Body Disease
-
Limb-girdle Muscular Dystrophy
-
Limb-girdle Muscular Dystrophy Type 2A
-
Limb-girdle Muscular Dystrophy Type 2E
-
Limb-girdle Muscular Dystrophy, Type 2C
-
Limb-girdle Muscular Dystrophy, Type 2D
-
Lipid Metabolism Disorders
-
Lithiasis
-
Liver Cirrhosis
-
Liver Cirrhosis, Biliary
-
Liver Diseases
-
Liver Failure
-
Liver Neoplasms
-
Low Back Pain
-
Low Tension Glaucoma
-
Lower Urinary Tract Symptoms
-
Lung Diseases
-
Lung Diseases, Interstitial
-
Lung Diseases, Obstructive
-
Lung Neoplasms
-
Lupus Erythematosus, Systemic
-
Lupus Nephritis
-
Lymphedema
-
Lymphoblastic Lymphoma
-
Lymphocytosis
-
Lymphohistiocytosis, Hemophagocytic
-
Lymphoma
-
Lymphoma, B-Cell
-
Lymphoma, Follicular
-
Lymphoma, Large B-Cell, Diffuse
-
Lymphoma, Mantle-Cell
-
Lymphosarcoma
-
Lysosomal Acid Lipase Deficiency
M
-
Macular Degeneration
-
Malignant Mesothelioma
-
Malocclusion
-
Mantle Cell Lymphoma
-
Maple Syrup Urine Disease
-
Marfan Syndrome
-
Mast Cell Activation Disorders
-
Mast Cell Activation Syndrome
-
Mastocytosis
-
Mastocytosis, Systemic
-
Mastodynia
-
Maturity-onset Diabetes of the Young
-
Medium-chain Acyl-coenzyme A Dehydrogenase Deficiency
-
Melanoma
-
Menkes Disease
-
Menkes Kinky Hair Syndrome
-
Mental Disorders
-
Mental Fatigue
-
Merkel Cell Carcinoma
-
Mesenteric Ischemia
-
Mesothelioma
-
Mesothelioma, Malignant
-
Metabolic Diseases
-
Metabolic Syndrome
-
Metachromatic Leukodystrophy
-
Methylmalonic Acidemia
-
Microscopic Polyangiitis
-
Microvascular Angina
-
Migraine Disorders
-
Mitochondrial Diseases
-
Mitochondrial Myopathies
-
Mitochondrial Trifunctional Protein Deficiency
-
Mitral Valve Insufficiency
-
Monoclonal Mast Cell Activation Syndrome
-
Motor Neuron Disease
-
Motor Skills Disorders
-
Mucopolysaccharidoses
-
Mucopolysaccharidosis
-
Mucopolysaccharidosis I
-
Mucopolysaccharidosis II
-
Mucopolysaccharidosis IV
-
Mucopolysaccharidosis Type I
-
Mucopolysaccharidosis Type II
-
Mucopolysaccharidosis Type IV
-
Mucopolysaccharidosis Type IVA
-
Mucopolysaccharidosis Type VI
-
Mucopolysaccharidosis Type VII
-
Mucopolysaccharidosis VI
-
Mucopolysaccharidosis VII
-
Mucositis
-
Multiple Carboxylase Deficiency
-
Multiple Myeloma
-
Multiple Sclerosis
-
Multiple Sclerosis, Chronic Progressive
-
Multiple Sclerosis, Relapsing-Remitting
-
Multiple System Atrophy
-
Muscle Spasticity
-
Muscle Weakness
-
Muscular Atrophy
-
Muscular Atrophy, Spinal
-
Muscular Diseases
-
Muscular Dystrophies
-
Muscular Dystrophies, Limb-Girdle
-
Muscular Dystrophy
-
Muscular Dystrophy, Duchenne
-
Musculoskeletal Diseases
-
Myasthenia Gravis
-
Myasthenic Syndromes, Congenital
-
Mycoses
-
Mydriasis
-
Myelodysplastic Syndrome With Excess Blasts
-
Myelodysplastic Syndromes
-
Myeloid Leukemia
-
Myeloproliferative Disorders
-
Myocardial Infarction
-
Myocardial Ischemia
-
Myocarditis
-
Myofascial Pain Syndromes
-
Myofibroma
-
Myositis
-
Myositis, Inclusion Body
N
-
N-acetylglutamate Synthase Deficiency
-
Nasal Obstruction
-
Nasal Polyps
-
Neck Pain
-
Necrosis
-
Necrotizing Fasciitis
-
Neoplasm Metastasis
-
Neoplasm, Residual
-
Neoplasms, Plasma Cell
-
Neoplasms, Second Primary
-
Nephritis
-
Nephritis, Hereditary
-
Nephrogenic Diabetes Insipidus
-
Nephrosis
-
Nephrotic Syndrome
-
Nerve Compression Syndromes
-
Nerve Degeneration
-
Nervous System Neoplasms
-
Nesidioblastosis
-
Neuralgia
-
Neuroblastoma
-
Neurocognitive Disorders
-
Neurodegenerative Diseases
-
Neurodevelopmental Disorders
-
Neuroendocrine Tumor
-
Neuroendocrine Tumors
-
Neurofibroma
-
Neurofibromatoses
-
Neurofibromatosis
-
Neurofibromatosis 1
-
Neurofibromatosis Type 1
-
Neurologic Manifestations
-
Neuromuscular Manifestations
-
Neuronal Ceroid Lipofuscinosis
-
Neuronal Ceroid-Lipofuscinoses
-
Neurotoxicity Syndromes
-
Neutropenia
-
Nocturia
-
Nocturnal Enuresis
-
Non-ST Elevated Myocardial Infarction
-
Non-alcoholic Fatty Liver Disease
O
-
Obesity
-
Obesity, Morbid
-
Obsessive-Compulsive Disorder
-
Optic Pathway Glioma
-
Orchitis
-
Ornithine Carbamoyltransferase Deficiency Disease
-
Ornithine Transcarbamylase Deficiency
-
Oropharyngeal Neoplasms
-
Osteoarthritis
-
Osteoarthritis, Hip
-
Osteoarthritis, Knee
-
Osteochondrodysplasias
-
Osteoporosis
-
Osteosarcoma
-
Ototoxicity
-
Out-of-Hospital Cardiac Arrest
-
Ovarian Cancer
-
Ovarian Epithelial Cancer
-
Ovarian Neoplasms
-
Overweight
P
-
PGM1-CDG
-
Pain, Intractable
-
Pain, Postoperative
-
Pancreatic Cancer
-
Pancreatic Neoplasms
-
Panic Disorder
-
Papilloma
-
Papillomavirus Infections
-
Paralysis
-
Paraplegia
-
Parasomnias
-
Paresis
-
Parkinson Disease
-
Paroxysmal Ventricular Fibrillation
-
Patent Ductus Arteriosus
-
Pediatric Obesity
-
Pelvic Organ Prolapse
-
Periodontitis
-
Peripheral Arterial Disease
-
Peripheral Nervous System Diseases
-
Peripheral Vascular Diseases
-
Peritoneal Neoplasms
-
Peritonitis
-
Peroneal Neuropathies
-
Phenylketonuria
-
Phenylketonurias
-
Phobic Disorders
-
Phosphoserine Aminotransferase Deficiency
-
Pick Disease of the Brain
-
Pituitary Diseases
-
Pleural Effusion
-
Pneumonia
-
Pneumoperitoneum
-
Pneumothorax
-
Poland Syndrome
-
Polyarteritis Nodosa
-
Polycystic Kidney Diseases
-
Polycystic Kidney, Autosomal Dominant
-
Polycystic Ovary Syndrome
-
Polycythemia
-
Polycythemia Vera
-
Polymyalgia Rheumatica
-
Polyneuropathies
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Polyps
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Popliteal Artery Aneurysm
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Post-Acute COVID-19 Syndrome
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Posterior Urethral Valves
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Postoperative Cognitive Complications
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Postoperative Complications
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Postoperative Hemorrhage
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Postural Orthostatic Tachycardia Syndrome
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Pre-Eclampsia
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Precursor Cell Lymphoblastic Leukemia-Lymphoma
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Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
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Preleukemia
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Premature Birth
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Presbycusis
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Presbyopia
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Pressure Ulcer
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Primary Agammaglobulinemia
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Primary Biliary Cholangitis
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Primary Carnitine Deficiency
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Primary Ciliary Dyskinesia
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Primary Dysautonomias
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Primary Hyperoxaluria Type 1
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Primary Lateral Sclerosis
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Primary Liver Cancer
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Primary Myelofibrosis
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Primary Progressive Aphasia
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Primary Sclerosing Cholangitis
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Prinzmetal's Variant Angina
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Problem Behavior
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Progressive Familial Intrahepatic Cholestasis 1
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Prolapse
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Propionic Acidemia
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Prostatic Neoplasms
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Prostatic Neoplasms, Castration-Resistant
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Prosthesis Failure
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Pruritus
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Pseudohypoaldosteronism
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Pseudomyxoma Peritonei
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Psoriasis
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Psoriatic Juvenile Idiopathic Arthritis
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Puerperal Disorders
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Pulmonary Arterial Hypertension
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Pulmonary Atelectasis
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Pulmonary Disease, Chronic Obstructive
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Pulmonary Edema
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Pulmonary Embolism
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Pulmonary Emphysema
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Pulmonary Fibrosis
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Pulmonary Heart Disease
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Pyloric Stenosis
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Pyridoxal 5'-phosphate-dependent Epilepsy
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Pyridoxine-dependent Epilepsy
R
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Radiculopathy
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Radiodermatitis
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Radius Fractures
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Rectal Diseases
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Rectal Neoplasms
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Rectovaginal Fistula
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Recurrence
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Refractive Errors
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Reinfection
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Renal Cell Carcinoma
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Renal Insufficiency
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Renal Insufficiency, Chronic
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Renal Tubular Acidosis
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Respiration Disorders
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Respiratory Aspiration
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Respiratory Distress Syndrome
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Respiratory Distress Syndrome, Infant
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Respiratory Distress Syndrome, Newborn
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Respiratory Insufficiency
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Respiratory Tract Diseases
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Retinal Degeneration
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Retinal Diseases
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Retinal Dystrophies
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Retinitis
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Retinitis Pigmentosa
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Retinoblastoma
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Rhinitis
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Rhinitis, Allergic
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Rhinitis, Allergic, Perennial
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Rhinitis, Allergic, Seasonal
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Rhinosinusitis
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Riboflavin Deficiency
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Riboflavin Transporter Deficiency
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Rotator Cuff Injuries
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Roussy Levy Syndrome
S
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SCOT Deficiency
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ST Elevation Myocardial Infarction
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Salivary Gland Neoplasms
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Salmonella Infections
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Sarcoglycanopathies
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Sarcoidosis
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Sarcoma
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Sarcoma, Endometrial Stromal
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Sarcoma, Ewing
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Sarcopenia
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Scleroderma, Diffuse
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Scleroderma, Systemic
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Sclerosis
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Scoliosis
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Semantic Dementia
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Sensation Disorders
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Sepiapterin Reductase Deficiency
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Sepsis
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Severe Acute Respiratory Syndrome
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Severe Combined Immunodeficiency
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Severe Congenital Neutropenia
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Sex Cord-Gonadal Stromal Tumors
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Shock
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Shock, Cardiogenic
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Short Bowel Syndrome
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Shoulder Impingement Syndrome
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Shoulder Pain
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Shwachman-Diamond Syndrome
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Shy-Drager Syndrome
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Sickle Cell Anemia
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Sinusitis
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Skin Diseases, Genetic
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Skin Neoplasms
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Sleep Apnea Syndromes
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Sleep Apnea, Central
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Sleep Apnea, Obstructive
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Sleep Disorders, Intrinsic
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Sleep Wake Disorders
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Small Cell Lung Cancer
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Small Cell Lung Carcinoma
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Small Intestinal Adenocarcinoma
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Small Intestine Cancer
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Smith-Lemli-Opitz Syndrome
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Soft Tissue Sarcoma
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Spermatic Cord Torsion
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Spinal Cord Injuries
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Spinal Muscular Atrophies of Childhood
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Spinal Muscular Atrophy
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Spinal Muscular Atrophy Type 3
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Spondylarthritis
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Spondylarthropathies
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Spondylarthropathy
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Spondylitis
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Spondylitis, Ankylosing
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Squamous Cell Carcinoma of Head and Neck
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Status Epilepticus
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Stiff-Person Syndrome
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Still's Disease, Adult-Onset
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Stomach Cancer
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Stomach Neoplasms
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Streptococcal Infections
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Stress Disorders, Post-Traumatic
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Stress Disorders, Traumatic
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Stress, Psychological
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Stroke
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Subarachnoid Hemorrhage
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Syndrome
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Systemic Candidiasis
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Systemic Mastocytosis
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Systemic Onset Juvenile Idiopathic Arthritis
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Systemic Scleroderma
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Systemic Vasculitis
T
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Tachycardia
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Tachycardia, Sinus
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Tachycardia, Supraventricular
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Tachycardia, Ventricular
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Tachypnea
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Takayasu Arteritis
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Tauopathies
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Tendinopathy
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Testicular Neoplasms
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Thalassemia
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Thoracic Neoplasms
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Thrombocythemia, Essential
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Thrombocytosis
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Thromboembolism
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Thrombosis
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Thymoma
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Thymus Neoplasms
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Thyroid Cancer, Medullary
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Thyroid Diseases
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Thyroid Neoplasms
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Timothy Syndrome
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Tinnitus
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Tissue Adhesions
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Tooth Diseases
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Tooth Wear
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Torsades de Pointes
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Transfusion Reaction
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Transient Tachypnea of the Newborn
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Transitional Cell Carcinoma
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Tricuspid Valve Insufficiency
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Triple Negative Breast Neoplasms
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Tuberous Sclerosis
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Tuberous Sclerosis Complex
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Typhoid Fever
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Tyrosine Hydroxylase Deficiency
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Tyrosinemia Type 1
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Tyrosinemia Type 2
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Tyrosinemia Type 3
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Tyrosinemias
U
V
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Varicocele
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Varicose Ulcer
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Vascular Calcification
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Vascular Diseases
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Vasculitis
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Vasospasm, Intracranial
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Venous Insufficiency
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Venous Thromboembolism
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Ventricular Fibrillation
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Ventricular Remodeling
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Vestibular Diseases
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Virus Diseases
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Visceral Steatosis
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Vision Disorders
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Vision, Low
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Vitamin B 12 Deficiency
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Vitamin D Deficiency
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Vitamin E Deficiency
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Voice Disorders
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Vomiting
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Von Willebrand Diseases
W