Related by context. All words. (Click for frequent words.) 69 Long QT syndrome 67 hypokalemia hypomagnesemia 67 Long QT Syndrome 64 LQTS 63 QT prolongation 63 arrhythmogenic right 63 polymorphic ventricular tachycardia 63 hypertrophic cardiomyopathy HCM 62 torsades de pointes 62 Brugada syndrome 61 torsade de pointes 61 arrhythmias 61 Brugada Syndrome 61 valvular disease 61 rhythm disturbances 60 heart arrhythmias 60 myotonic dystrophy 60 hyperkalemia 60 sustained ventricular tachycardia 60 Torsades de Pointes 60 nonischemic 60 familial hypercholesterolemia 59 Polymorphic Ventricular Tachycardia CPVT 59 IgA deficiency 59 thrombophilia 59 optic neuropathy 59 aortic stenosis 59 familial adenomatous polyposis 59 primary pulmonary hypertension 59 cardiac abnormalities 59 spinocerebellar ataxia 59 ventricular arrhythmia 59 ventricular arrhythmias 58 QT intervals 58 cardiac hypertrophy 58 Von Willebrand disease 58 ventricular tachycardia VT 58 Cowden syndrome 58 G6PD deficiency 58 prolonged QT interval 58 ventricular fibrillation VF 58 QTc interval 58 hydrops 58 kidney insufficiency 58 ventricular fibrillation 58 artery occlusion 58 methemoglobinemia 58 sudden cardiac death 58 syncope 58 Eisenmenger syndrome 58 abnormalities 58 left ventricular dysfunction 58 bronchopulmonary dysplasia 57 ventricular tachycardia 57 acute aortic dissection 57 thyroid dysfunction 57 cardiomyopathies 57 dilated cardiomyopathy 57 Hurler syndrome 57 thromboembolism 57 hyperpyrexia 57 Hashimoto thyroiditis 57 valvular heart disease 57 congenital anomaly 57 atresia 57 persistent pulmonary hypertension 57 cardiac insufficiency 57 decompensated heart failure 57 ARVD 57 Postoperative complications 57 pyloric stenosis 57 necrotizing pancreatitis 57 hypertrophic cardiomyopathy 57 auditory neuropathy 57 tachyarrhythmias 57 hemochromatosis 57 arrythmia 57 Dravet syndrome 57 genetic syndromes 57 immunodeficiencies 57 aortic rupture 57 transfusion syndrome 57 cardiovascular disease cerebrovascular disease 57 QTc prolongation 57 genetic abnormality 57 malignant hyperthermia 57 arrhythmia 57 Raynaud disease 57 cardiomyopathy 57 ischemic colitis 57 Ventricular fibrillation 57 renal dysfunction 56 blood clotting disorder 56 hemolytic anemia 56 thyrotoxicosis 56 Chiari malformation 56 autosomal dominant 56 postoperative AF 56 supraventricular tachycardia 56 silent ischemia 56 achondroplasia 56 acute phosphate nephropathy 56 polycystic ovary syndrome 56 atrial fibrillation 56 Li Fraumeni syndrome 56 SCN5A 56 pulmonary atresia 56 rhythm abnormalities 56 asystole 56 ventricular dysplasia 56 pulmonary thromboembolism 56 lichen planus 56 unprovoked seizures 56 preserved ejection fraction 56 hamartomas 56 paraganglioma 56 basal cell nevus syndrome 56 dyskeratosis congenita 56 unknown etiology 56 temporal arteritis 56 cardiac arrhythmias 56 congenital hypothyroidism 56 sporadic Creutzfeldt Jakob 56 familial ALS 56 Wegener granulomatosis 56 metabolic acidosis 56 ADPKD 56 myocardial ischemia 56 ventricular cardiomyopathy 56 primary ciliary dyskinesia 56 Arrhythmogenic Right Ventricular Cardiomyopathy 56 Leber congenital amaurosis 56 cardioembolic stroke 56 chronic metabolic acidosis 56 tricuspid atresia 56 inherited mutations 56 autosomal dominant disorder 56 autoimmune hemolytic anemia 56 thromboses 56 subarachnoid hemorrhages 56 left ventricular hypertrophy 56 syncopal episodes 56 galactosemia 56 microbleeds 56 precancerous colon polyps 56 ventricular tachyarrhythmias 56 pericardial effusions 56 intractable epilepsy 56 Alport syndrome 55 Hurthle cell 55 Pulmonary hypertension 55 vasovagal syncope 55 chromosomal defect 55 status epilepticus 55 nonarteritic anterior ischemic optic 55 Hyperkalemia 55 untreated sleep apnea 55 holoprosencephaly 55 heart arrhythmia 55 NF1 55 coronary artery disease 55 thrombotic events 55 Moyamoya disease 55 congential 55 heterotaxy 55 colon perforation 55 MYCN amplification 55 ICD shocks 55 leukoencephalopathy 55 de ath 55 Epileptic seizures 55 hereditary disorder 55 Reye syndrome 55 fulminant hepatitis 55 renal insufficiency 55 cardiac arrhythmia abnormal 55 QT interval 55 diabetes mellitus T2DM 55 cardiac conduction 55 hypersensitivity reaction 55 thrombotic thrombocytopenic purpura TTP 55 Aortic stenosis 55 electrolyte disturbances 55 subclinical hyperthyroidism 55 inherited retinal degeneration 55 abnormal genital 55 Vitamin B# deficiency 55 cause cardiac channelopathies 55 Lafora disease 55 Cushing syndrome 55 unexplained fainting 55 autoimmune thyroid 55 Hypertrophic cardiomyopathy 55 dysrhythmia 55 diaphragmatic hernia 55 von Willebrand disease 55 neurological abnormalities 55 idiopathic pulmonary 55 intraventricular hemorrhage 55 GH deficiency 55 clotting disorder 55 Severe Primary IGFD 55 Hyperthyroidism 55 hyperprolactinemia 55 idiopathic 54 juvenile myelomonocytic leukemia 54 congenital abnormalities 54 primary ovarian insufficiency 54 Myocarditis 54 Marfan syndrome 54 chronic granulomatous disease 54 amenorrhoea 54 spinal muscle atrophy 54 chromosome abnormality 54 sCJD 54 ABCB1 54 endometrial hyperplasia 54 intestinal polyps 54 cardiac arrythmia 54 CPVT 54 microvascular disease 54 Pulmonary embolism 54 progressive neurodegenerative disorder 54 Nephrogenic Systemic Fibrosis NSF 54 idiopathic generalized epilepsy 54 Hypotension 54 AAT deficiency 54 hypopituitarism 54 neurological complications 54 acute myocarditis 54 Hemorrhagic strokes 54 myelomeningocele 54 adrenal insufficiency 54 ectodermal dysplasia 54 pulmonary emboli 54 haloperidol Haldol 54 carotid stenosis 54 Churg Strauss syndrome 54 Hirschsprung disease 54 systemic scleroderma 54 lactic acidosis 54 induce orthostatic hypotension 54 bowel perforations 54 myelodysplasia 54 Leber congenital amaurosis LCA 54 Retinopathy 54 hypoxemia 54 sinus node dysfunction 54 variant angina 54 hereditary disorders 54 Kufs disease 54 Reye Syndrome 54 Atrial fibrillation AF 54 Tachycardia 54 uremia 54 urolithiasis 54 multisystem disease 54 aortic valve stenosis 54 spastic diplegia 54 thromboembolic 54 homozygous familial hypercholesterolemia 54 loop diuretics 54 cortical dysplasia 54 proliferative retinopathy 54 Hypertrophic Cardiomyopathy 54 hyperparathyroidism 54 pulmonary artery hypertension 54 pacemaker implantation 54 cerebral vascular disease 54 MCAD deficiency 54 achalasia 54 arrythmias 54 paroxysmal AF 54 atrial septal 54 microvascular angina 54 repolarization 54 DiGeorge syndrome 54 Fragile X Syndrome 54 anoxic brain injury 54 infantile onset 54 coagulation abnormalities 54 arrhythmogenic 54 flecainide 54 recurrent wheezing 54 Congenital Adrenal Hyperplasia 54 abnormal heartbeats 54 cerebral infarction 54 bowel perforation 54 ataxias 54 threatening arrhythmias 54 familial pancreatic cancer 54 neuroleptic malignant syndrome 54 progressive dyspnea 54 antiarrhythmic medications 54 QT interval prolongation 54 nerve degeneration 54 ICDs implanted 54 electrolyte abnormalities 54 motor neuron degeneration 54 myocarditis 54 Fanconi anemia 54 pulmonary hypertension PH 54 pulmonary hypertension 54 Usher Syndrome 54 Rhabdomyolysis 53 idiopathic dilated cardiomyopathy 53 cardiomegaly 53 congenital disorder 53 cerebral thrombosis 53 systolic dysfunction 53 chorioamnionitis 53 situs inversus 53 cardiac tamponade 53 neurologic abnormalities 53 angiosarcoma 53 ventricular septal defect VSD 53 esophageal atresia 53 hemophagocytic lymphohistiocytosis 53 vWD 53 Cardiac arrhythmia 53 vertebral artery dissection 53 vascular cognitive impairment 53 Hypertrophic Cardiomyopathy HCM 53 fatal arrhythmias 53 MGUS 53 subaortic stenosis 53 cardiac arrhythmia 53 dominantly inherited 53 von Willebrand 53 transient ischemic attacks 53 vascular disease 53 myocardial fibrosis 53 beta blocker therapy 53 de novo mutations 53 Ventricular Tachycardia 53 noncardiovascular 53 interstitial lung disease 53 gastrointestinal stromal tumor 53 cryptogenic stroke 53 ischemic strokes 53 angina chest 53 subarachnoid haemorrhage 53 abnormal rhythms 53 ataxia telangiectasia 53 syncopal episode 53 SNHL 53 CHD7 53 cerebrovascular events 53 chromosomal disorder 53 adenomatous polyps 53 testicular tumors 53 osteogenesis imperfecta 53 atrial arrhythmias 53 T1DM 53 hyperemesis 53 ARVC 53 degenerative neurological disease 53 Chiari Malformation 53 homozygous FH 53 medium chain acyl 53 TEAEs 53 syncopal 53 Bullous 53 cerebrovascular accidents 53 liver dysfunction 53 gastric reflux 53 neurologic deficits 53 MULTAQ 53 hamartoma 53 Pervasive Developmental Disorder 53 deep vein thromboses 53 diabetes mellitus DM 53 cardiac channelopathies 53 Tardive dyskinesia 53 bullous 53 hypertrophic obstructive cardiomyopathy 53 FXTAS 53 arterial calcification 53 AIOD 53 neurologic symptoms 53 non arteritic anterior ischemic 53 ketoacidosis 53 sortilin 53 encephalitis meningitis 53 infection progressive multifocal 53 patent ductus arteriosus 53 Leber hereditary optic neuropathy 53 cerebrovascular accident 53 mental retardation epilepsy 53 non valvular atrial 53 hemolytic disease 53 cerebral vasospasm 53 arterial fibrillation 53 hippocampal function 53 noncardiac 53 pernicious anemia 53 ambiguous genitalia 53 bradycardia 53 benign positional vertigo 53 giant cell arteritis 53 epididymitis 53 postoperative delirium 53 Glioblastoma Multiforme GBM 53 hereditary predisposition 53 COREG 53 Vascular dementia 53 primary generalized tonic 53 lightheadedness fainting 53 idiopathic cardiomyopathy 53 carcinoid tumor 53 myopia nearsightedness 53 sinus node 53 #q# deletion 53 myelofibrosis polycythemia vera 53 thromboembolic events 53 osteopetrosis 53 thoracic aortic aneurysm 53 dermopathy 53 hypogonadotropic hypogonadism 53 subclinical hypothyroidism 53 CDH1 53 intracerebral 53 optica 53 benign paroxysmal positional vertigo 53 severe obstructive pulmonary 53 colorectal adenoma 53 microdeletion 53 chromosomal abnormality 53 pulseless electrical activity 53 aneuploidies 53 dermatologic reactions 53 APOE gene 53 stroke hypertension palpitations 53 asthma exacerbation 53 Ectopia Cordis 53 Obstructive sleep apnea 52 Rh incompatibility 52 phenylketonuria 52 cerebral embolism 52 nitrofurantoins 52 myeloproliferative neoplasms 52 preeclampsia 52 Intussusception 52 silent myocardial ischemia 52 TP# mutations 52 venous thrombosis 52 Cockayne syndrome 52 APOL1 52 cryptorchidism 52 stress cardiomyopathy 52 congenital deficiency 52 urinary blockage 52 subarachnoid 52 EXJADE 52 Hemochromatosis 52 genetic defect 52 sudden sensorineural hearing 52 Idiopathic 52 recurrent miscarriages 52 recurrent atrial fibrillation 52 bicuspid valve 52 CMV infection 52 Joubert syndrome 52 corticosteroid therapy 52 BRCA mutations 52 Myasthenia gravis 52 interstitial pneumonitis 52 pseudotumor cerebri 52 angiotensin receptor blockers 52 chromosomal aberrations 52 atrophic gastritis 52 vasa previa 52 acute colitis 52 generalized seizures 52 APOE e4 52 electrophysiologic 52 congenital disorders 52 complement inhibitor eculizumab 52 Peutz Jeghers syndrome 52 glomerulonephritis 52 sporadic ALS 52 irregular heartbeats 52 Autoimmune disorders 52 abnormal heartbeat 52 gastro oesophageal reflux disease 52 Wernicke Korsakoff syndrome 52 mosaicism 52 VIIBRYD 52 anemias 52 pathologic fracture 52 Cardiac arrhythmias 52 autoinflammatory diseases 52 laryngospasm 52 sinus tachycardia 52 hepatic dysfunction 52 Diabetic neuropathy 52 seizures comas 52 hereditary deafness 52 eosinophilic pneumonia 52 hypovolemic shock 52 polycystic ovarian syndrome PCOS 52 Acute pancreatitis 52 structural abnormalities 52 Mitochondrial diseases 52 enteropathy 52 Hyperplasia 52 kidney dysfunction 52 parathyroid 52 Leber Congenital Amaurosis LCA 52 cardiac dysfunction 52 cerebral ischemia 52 tardive dyskinesia TD 52 antiepileptic medications 52 BRCA1 mutations 52 Persistent Pulmonary Hypertension 52 cardiogenic shock 52 AAT Deficiency 52 recessive trait 52 juvenile myoclonic epilepsy 52 genetic abnormalities 52 mycosis fungoides 52 lacunar 52 epilepsy 52 implanted pacemakers 52 precocious puberty 52 hemorrhagic strokes 52 Hypoglycemia 52 lymphangioleiomyomatosis LAM 52 nonmelanoma skin cancers 52 Kabuki syndrome 52 syncope fainting 52 salmeterol HFA MDI 52 Lactic acidosis 52 biliary atresia 52 airway hyperresponsiveness 52 microalbuminuria 52 carotid artery blockage 52 coronary thrombosis 52 retinal dystrophy 52 G#S mutation 52 TACI mutations 52 bicuspid aortic valve 52 Anencephaly 52 genetic neuromuscular disorder 52 polycystic kidneys 52 sensorineural hearing loss 52 cerebri 52 Hemorrhagic stroke 52 recessive inheritance 52 PTEN mutation 52 Hip dysplasia 52 hepatic toxicity 52 monogenic 52 IUGR 52 ACTOplus met XR 52 essential thrombocythemia 52 cerebrovascular disease 52 BPPV 52 treat brain aneurysms 52 antithrombin deficiency 52 hepatic failure 52 thyroiditis 52 Arnold Chiari Malformation 52 hypercoagulable 52 retinopathy 52 Ebstein anomaly 52 genetic polymorphism 52 mitochondrial dysfunction 52 endothelial dysfunction 52 vitamin B# deficiency 52 retinal degeneration 52 arteriovenous malformations 52 leptin deficiency 52 tachycardias 52 T wave alternans 52 brain malformation 52 Arrhythmias 52 myotonic muscular dystrophy 52 hypoperfusion 52 obstructive sleep apnea 52 heparin induced thrombocytopenia 52 polycystic ovarian disease 52 colorectal polyps 52 post thrombotic syndrome 52 choroidal neovascularization 52 artery stenosis 52 bronchogenic carcinoma 52 underactive thyroid gland 52 Tasigna prolongs 52 Thrombocytopenia 52 PR interval prolongation 52 truncus arteriosus 52 Hutchinson Gilford progeria 52 proliferative diabetic retinopathy 52 dopaminergic therapy 52 induced ischemia 52 fronto temporal dementia 52 primary aldosteronism 52 renal scarring 52 Ketoacidosis 52 thrombocytosis 52 hypoglycemic episodes 52 β blockers 52 immunodeficiency 52 achromatopsia 52 underwent coronary angiography 52 diastolic dysfunction 52 coronary disease 52 Atrial Septal Defect 52 frontotemporal dementia 52 Dilated cardiomyopathy 52 DiGeorge Syndrome 52 papillary carcinoma 52 PTLD 52 pulmonary edema 52 aortic aneurysms 52 azoospermia 52 cytopenias 52 Klinefelter syndrome 52 haemochromatosis 52 neurofibromas 52 Generalized anxiety disorder 52 mitral valve regurgitation 52 clefting 52 alkalosis 52 mitral valve prolapse 52 electrocardiogram EKG 52 APOE ε4 52 chronic eosinophilic leukemia 52 Tay Sachs thalassemia 52 dysglycemia 52 regulator CFTR gene 52 electrical conduction 52 lactase deficiency 51 transcranial Doppler ultrasound 51 Medulloblastoma 51 atrial tachyarrhythmias 51 Maroteaux Lamy syndrome 51 hypothalamic pituitary adrenal axis 51 hereditary antithrombin deficiency 51 ECG abnormalities 51 NYHA Class II 51 undergoing coronary artery 51 alpha thalassemia 51 myasthenia gravis 51 epigenetic changes 51 esophagitis 51 abnormal uterine bleeding 51 atypical hemolytic uremic syndrome 51 gouty arthritis 51 tachyarrhythmia 51 Severe hypoglycemia 51 hypercalcemia 51 efalizumab 51 RPE# 51 Heavy menstrual bleeding 51 impaired cognition 51 pathophysiologic 51 juvenile idiopathic arthritis 51 ruptured brain aneurysm 51 thyroid deficiency 51 untreated celiac disease 51 Wernicke encephalopathy 51 idiopathic PAH 51 patent foramen ovale 51 brain lesions 51 mitochondrial abnormalities 51 AV node 51 extrapyramidal symptoms 51 atrial septal defect 51 autosomal dominant inheritance 51 ependymoma 51 bypass grafting 51 Erythropoietic therapies may 51 intensive statin therapy 51 hemorrhagic bleeding 51 choriocarcinoma 51 pulmonary hemorrhage 51 colorectal adenomas 51 congenital malformations 51 Compulsive hoarding 51 myopathies 51 JAK2 mutation 51 reflux disease 51 alpha1 antitrypsin deficiency 51 pericardial effusion 51 metabolic disorder 51 muscular dystrophies 51 lysosomal storage disease 51 poor metabolizers 51 Myelodysplastic Syndrome 51 paraneoplastic 51 acute decompensation 51 intracerebral haemorrhage 51 ethosuximide 51 Henoch purpura 51 hereditary hemorrhagic telangiectasia 51 malformations 51 suppurative 51 Tambocor 51 Polycystic ovary syndrome 51 ischemic cardiac 51 Zollinger Ellison syndrome 51 V Leiden 51 spastic paraplegia 51 hyponatraemia 51 mtDNA mutations 51 kidney urologic 51 febrile convulsions 51 CHARGE syndrome 51 Asymptomatic 51 diabetic kidney 51 neural tube defect 51 Obstructive sleep apnea OSA 51 pathologic fractures 51 TCF#L# gene 51 upper gastrointestinal bleeding 51 carotid artery ultrasound 51 congenital anomalies 51 recurrent seizures 51 cTnT 51 ANCA associated 51 Niemann Pick disease 51 polyomavirus nephropathy 51 myocardial infarction congestive heart 51 myoclonic seizures 51 unruptured aneurysm 51 blastoma 51 radioiodine therapy 51 aniridia 51 autosomal recessive 51 epilepsies 51 benazepril 51 hypoplasia 51 cytogenetic abnormalities 51 periodontitis 51 chronic thromboembolic pulmonary 51 Haptoglobin 51 Hirschsprung Disease 51 myalgic encephalomyelitis ME 51 nonsense mutation 51 prematurity ROP 51 Fas ligand 51 Sjögren syndrome 51 chronic GVHD 51 disseminated intravascular coagulation 51 cardiac arrythmias 51 postoperative pulmonary 51 erythematosus 51 asymptomatic carotid stenosis 51 CMV infections 51 Malformation 51 amiodarone 51 QT syndrome 51 chronic renal insufficiency 51 airway blockage 51 upper airway obstruction 51 renovascular hypertension 51 dentinal hypersensitivity 51 herpes infection 51 afib 51 prosopagnosia 51 Cystic fibrosis CF 51 dissociative disorders 51 thrombotic complications 51 petit mal seizures 51 Polycystic ovary syndrome PCOS 51 Prostatitis 51 Ischemia 51 immunodeficiency disorder 51 debilitating complication 51 Retinoblastoma 51 severe respiratory distress 51 immune thrombocytopenic purpura 51 nonmelanoma skin cancer 51 cryptogenic 51 vasospasm 51 infectious mononucleosis 51 occlusive disease 51 metabolic abnormality 51 nephrogenic fibrosing dermopathy 51 hypercoagulability 51 toxic epidermal necrolysis TEN 51 Benign Paroxysmal Positional Vertigo 51 Abbott Laboratories Norvir 51 atherosclerotic disease 51 hematuria 51 aneurysmal subarachnoid hemorrhage 51 serotonin syndrome 51 Joubert syndromes 51 mitochondrial disease 51 hyperreflexia 51 autoimmune reactions 51 hypoxic encephalopathy 51 VT VF 51 warfarin therapy 51 deafness neurological 51 intracerebral hemorrhage 51 atrial septal defects 51 neurologic complications 51 TP# mutation 51 histiocytosis 51 pheochromocytomas 51 hypertension 51 Apert syndrome 51 Mitral regurgitation 51 electrocardiography 51 abnormal growths 51 hyperplastic 51 placental abruption 51 MYH9 gene 51 hepatic impairment 51 dysrhythmias 51 adenomyosis 51 necrotizing pneumonia 51 torticollis 51 vascular dysfunction 51 conduction abnormalities 51 lung biopsy 51 growth restriction IUGR 51 febrile seizure 51 thiazide diuretic 51 cortical blindness 51 hypoventilation 51 motor neuron diseases 51 beta thalassemia 51 mitral stenosis 51 familial hypercholesterolaemia FH 51 lissencephaly 51 sinus bradycardia 51 immunosuppressive medications 51 electrical cardioversion 51 pancytopenia 51 gastrointestinal obstruction 51 neurologic sequelae 51 mutated BRCA 51 abnormal vaginal bleeding 51 agenesis 51 Ischemic strokes 51 cardiac troponin 51 nonvascular 51 levodopa therapy 51 adrenocortical cancer 51 NKX2 51 bacterial endocarditis 51 Subarachnoid hemorrhage 51 HELLP 51 thrombosis 51 Arrhythmogenic 51 Glucocorticoids 51 TNF antagonist 51 ectopic 51 bronchopulmonary dysplasia BPD 51 mesenteric ischemia 51 convulsive seizures 51 Gynecomastia 51 infective endocarditis 51 vascular disorders 51 periodontal infections 51 degenerative neurological diseases 51 involuntary tics 51 asthma bronchitis emphysema 51 LRAT 51 mitochondrial diseases 51 uncontrolled epilepsy 51 Idiopathic Thrombocytopenic Purpura 51 leiomyomas 51 chromosomal anomaly 51 generalized epilepsy 51 Systemic lupus erythematosus 51 habitual snoring 51 Charcot foot 50 Crouzon Syndrome 50 without uremia 50 APOE4 50 cytopenia 50 NOMID 50 infarction 50 static encephalopathy 50 WAGR syndrome 50 angina pectoris 50 recurrent infections 50 overt nephropathy 50 optic neuritis 50 dilated cardiomyopathy DCM 50 atherosclerotic cardiovascular disease 50 acute porphyria 50 Digoxin toxicity 50 Myotonic dystrophy 50 FASPS 50 anticonvulsant drugs 50 onset diabetes mellitus 50 vascular abnormalities 50 optic nerve hypoplasia 50 Peripheral neuropathy 50 degenerative disorder 50 polycystic ovary syndrome PCOS 50 enteroviral infection 50 Ischemic stroke 50 interrupted aortic arch 50 gestational diabetes mellitus 50 preserved systolic 50 ruptured aneurysms 50 angioedema 50 myopathy 50 cholinesterase inhibitor 50 acute ischemia 50 carotid artery stenosis 50 nonalcoholic steatohepatitis 50 ORMDL3 50 cerebral microbleeds 50 unstable angina UA 50 photosensitivity 50 fibrillation 50 thromboembolic complications 50 HNPCC 50 BRCA2 gene 50 variable immunodeficiency 50 retinal detachment 50 anencephaly 50 prolonged QT intervals 50 myelodysplastic syndrome MDS 50 Lennox Gastaut syndrome 50 Pulmonary arterial hypertension 50 allograft rejection 50 premalignant 50 bicuspid aortic valves 50 neuro degenerative 50 polymyalgia rheumatica 50 abdominal CT scans 50 myocardial infarctions 50 degenerative neurological disorder 50 vascular occlusive diseases 50 LRP5 50 thoracic aortic disease 50 autonomic dysfunction 50 renal impairment 50 Rh factor 50 paroxysmal atrial fibrillation 50 dopamine receptor gene 50 varices 50 coronary artery dissection 50 coronary artery blockages 50 Avascular necrosis 50 cerebral vascular accident 50 bladder exstrophy 50 malperfusion 50 eosinophilic 50 neonatal encephalopathy 50 bleeding diathesis 50 granulomatous 50 HBV infection 50 Lennox Gastaut Syndrome 50 antidiuretic hormone 50 Atrial fibrillation 50 myeloproliferative diseases 50 polycystic disease 50 Acute Exacerbations 50 metabolic disturbances 50 Myocardial infarction 50 optic neuropathy NAION 50 coronary angiography 50 enterovirus infection 50 restrictive cardiomyopathy 50 pleural mesothelioma 50 hyperthyroidism 50 disease Chronic Traumatic 50 pyelonephritis 50 epidermolysis bullosa EB 50 EEGs 50 GRK5 50 gallstone disease 50 behavioral abnormalities 50 postoperative complication 50 milrinone 50 onset sepsis 50 Syndrome SADS 50 D dimer 50 intraventricular 50 pheochromocytoma 50 atherothrombosis 50 eosinophilic esophagitis 50 Dysplasia 50 Sleep disordered breathing 50 Aortic dissection 50 SRBD 50 polycystic 50 tibolone 50 hypoglycemic coma 50 ictal 50 intermittent claudication 50 artery calcification 50 EEG abnormalities 50 fibrous dysplasia 50 irregular quivering 50 lipid lowering drugs 50 Perthes disease 50 bacterial prostatitis 50 ApoE4 gene