Related by context. All words. (Click for frequent words.) 67 ADPKD 67 ARVD 66 familial ALS 66 thrombophilia 66 Brugada syndrome 65 AAT deficiency 65 familial pancreatic cancer 65 BRCA mutations 65 T1DM 65 sporadic ALS 65 MGUS 65 HNPCC 65 mtDNA mutations 65 familial adenomatous polyposis 65 subclinical hyperthyroidism 65 APOE e4 65 sCJD 65 BRCA1 mutations 65 familial hypercholesterolemia 64 elevated triglyceride levels 64 cardioembolic stroke 64 GISTs 64 Brugada Syndrome 64 microalbuminuria 64 NAFLD 64 long QT syndrome 64 CYP#C# [001] 64 subclinical atherosclerosis 64 MSH2 64 MYH9 gene 64 NOMID 63 vWD 63 APOE4 63 Retinopathy 63 beta thalassemia 63 ICDs implanted 63 genetic syndromes 63 carotid stenosis 63 spinocerebellar ataxia 63 GBA mutations 63 APOE genotype 63 inherited mutations 63 arterial calcification 63 cognitively normal 63 Haptoglobin 63 ependymoma 63 squamous cell lung cancer 63 airway hyperresponsiveness 63 APOE ε4 62 Prehypertension 62 narcolepsy cataplexy 62 hereditary breast cancer 62 Hemochromatosis 62 polymorphic ventricular tachycardia 62 subclinical hypothyroidism 62 prostate cancer CaP 62 adenomatous polyps 62 advanced neoplasia 62 CMV infection 62 troponin T 62 basal cell nevus syndrome 62 chromosomal aberrations 62 telomere lengths 62 IgA deficiency 62 microdeletions 62 pleural mesothelioma 62 chlamydial infection 62 colorectal cancer CRC 62 BRCA mutation 62 aneuploidies 62 prolonged QT interval 62 colorectal neoplasia 62 microbleeds 62 Peutz Jeghers syndrome 62 APOE gene 62 sudden cardiac death 62 K ras mutations 62 progressive neurodegenerative disorder 62 atherothrombotic disease 61 de novo mutations 61 recurrent VTE 61 SCN5A 61 diabetes mellitus DM 61 monoclonal gammopathy 61 nonmelanoma skin cancers 61 atherothrombosis 61 immunocompetent 61 recurrent miscarriage 61 MCAD deficiency 61 NF1 61 somatic mutations 61 brain lesions 61 TP# mutation 61 cardiac channelopathies 61 atherogenic dyslipidemia 61 Sudden Cardiac Death 61 HIV HCV coinfected 61 euthymic patients 61 leiomyomas 61 coronary calcification 61 renal cell carcinomas 61 pilocytic astrocytomas 61 hereditary predisposition 61 Hypertrophic cardiomyopathy 61 G#S mutation 61 Arrhythmias 61 cardiac dysfunction 61 PTPN# 61 HER2 overexpression 61 persistent pulmonary hypertension 61 arrhythmogenic right 61 myeloproliferative neoplasms 61 de ath 61 Adenomas 61 carcinoid 61 malignant lymphoma 61 SRBD 61 cTnT 61 EoE 61 habitual snoring 61 Hashimoto thyroiditis 61 recurrent miscarriages 61 Aortic stenosis 61 CC genotype 61 MLH1 61 heart arrhythmias 61 thoracic aortic disease 61 lung adenocarcinoma 61 decompensated heart failure 61 cryptogenic stroke 61 TPMT 61 ARVC 60 Genetic predisposition 60 hydrops 60 pathogenic mutations 60 myotonic dystrophy 60 FTLD 60 LV dysfunction 60 pancreatic adenocarcinoma 60 extrapyramidal symptoms 60 Cholangiocarcinoma 60 dysglycemia 60 chromosomal defect 60 coronary artery disease 60 thyroid dysfunction 60 Polycystic ovary syndrome PCOS 60 chromosomal rearrangement 60 Eisenmenger syndrome 60 Generalized anxiety disorder 60 LRRK2 mutations 60 germline mutations 60 hypertrophic cardiomyopathy HCM 60 genes BRCA1 60 T2DM 60 NGAL 60 Klinefelter syndrome 60 ApoE gene 60 postoperative delirium 60 chromosome abnormality 60 postoperative complication 60 VUR 60 heterotaxy 60 CPVT 60 Genetic variants 60 ApoE4 gene 60 CIN2 + 60 pyelonephritis 60 DNA methylation patterns 60 Leber congenital amaurosis LCA 60 genetic abnormalities 60 Long QT Syndrome 60 Vitamin B# deficiency 60 microvascular disease 60 lobular breast cancer 60 Cowden syndrome 60 coagulation abnormalities 60 G6PD deficiency 60 Hp2 2 60 untreated celiac disease 60 gallstone disease 60 antiphospholipid syndrome 60 obstructive sleep apnea 60 autonomic dysfunction 60 varicoceles 60 #q# deletion 60 systolic dysfunction 60 disease NAFLD 60 left ventricular dysfunction 60 chromosomal abnormalities 60 Pulmonary hypertension 60 FMR1 gene 60 intensive statin therapy 60 colorectal adenoma 60 seropositivity 60 asymptomatic carotid stenosis 60 hereditary hemochromatosis 60 KRAS mutation 60 lymphangioleiomyomatosis LAM 60 aortic valve stenosis 60 FMRP protein 60 polycystic ovary syndrome PCOS 60 AAT Deficiency 60 transcranial Doppler ultrasound 60 Hurler syndrome 60 bronchopulmonary dysplasia 60 genetic polymorphisms 60 Hurthle cell 60 JMML 60 EBV infection 60 untreated sleep apnea 60 aneuploidy 60 proband 60 2 diabetes T2D 60 KRAS mutations 60 aortic stenosis 60 poor metabolizers 60 nonmelanoma skin cancer 59 aortic atherosclerosis 59 MYH9 59 preserved ejection fraction 59 CDH1 59 Dravet syndrome 59 IKZF1 59 proliferative retinopathy 59 epigenetic changes 59 undiagnosed celiac disease 59 ventricular dysplasia 59 CHDs 59 Dilated Cardiomyopathy 59 endometrial hyperplasia 59 monogenic 59 Prostatitis 59 HNSCC 59 NF2 59 Uterine cancer 59 ductal cancer 59 QT intervals 59 BRCA mutation carriers 59 irreversible blindness 59 familial AF 59 bronchial hyperresponsiveness 59 frontotemporal dementia 59 V Leiden 59 VT VF 59 RSV infections 59 myelomeningocele 59 BRAF gene 59 infarcts 59 Acute myeloid leukemia 59 electrophysiologic 59 nonalcoholic steatohepatitis 59 chromosomal disorders 59 CP CPPS 59 CYP#D# 59 colorectal adenomas 59 BRCA gene mutation 59 EGFR mutations 59 APOE allele 59 BRCA2 gene mutation 59 QTc prolongation 59 renal artery stenosis 59 Polycystic Ovarian Syndrome PCOS 59 ApoE4 59 proliferative diabetic retinopathy 59 cerebral infarction 59 Heavy menstrual bleeding 59 gene mutations 59 extracolonic findings 59 Premature Ovarian Failure 59 #q#.# [001] 59 VKORC1 59 autosomal dominant 59 HBV infection 59 Thyroid disorders 59 TACI mutations 59 Squamous 59 APOL1 59 systemic amyloidosis 59 atrophic gastritis 59 unprovoked seizures 59 thiopurine 59 GIST tumors 59 QTc interval 59 genetic abnormality 59 autosomal dominant disorder 59 BRCA carriers 59 LTBI 59 mutations 59 HBsAg 59 HbF 59 IDH1 59 Afib 59 missense mutations 59 Alzheimer pathology 59 diagnose Alzheimer disease 59 sickle cell disease 59 advanced adenomas 59 neurological abnormalities 59 gene mutation 59 metabolic abnormalities 59 diabetic kidney 59 LHON 59 cardiomyopathies 59 underwent coronary angiography 59 transfusion syndrome 59 asymptomatic PAD 59 Cytogenetic 59 microscopic hematuria 59 paraganglioma 59 precancerous cervical 59 FSGS 59 epilepsies 59 elevated CRP 59 torsade de pointes 59 fatal neuromuscular disorder 59 microsatellite instability 59 thrombotic thrombocytopenic purpura TTP 59 nondemented 59 VCFS 59 genetic variants associated 58 lipid abnormalities 58 osteoporotic vertebral fractures 58 Pleural Mesothelioma 58 PPCM 58 Lung transplantation 58 Joubert syndrome 58 dyskeratosis congenita 58 spontaneous preterm birth 58 primary aldosteronism 58 uncontrolled epilepsy 58 sensorineural hearing loss 58 retinal degeneration 58 smoldering myeloma 58 coronary disease 58 nonischemic 58 familial clustering 58 rs# [002] 58 POAG 58 hamartomas 58 transcranial Doppler 58 vasa previa 58 ABCB1 58 clinico pathological 58 post thrombotic syndrome 58 apoE4 58 Hutchinson Gilford progeria 58 malignant neoplasm 58 LVNC 58 venous thrombosis 58 primary ovarian insufficiency 58 systemic lupus erythematosus SLE 58 silent myocardial ischemia 58 CYP#C# [002] 58 CYP#C# gene 58 neurologic complications 58 amnestic MCI 58 atypical hyperplasia 58 perfusion abnormalities 58 CFTR gene 58 Myelodysplastic syndromes MDS 58 autosomal dominant inheritance 58 arrhythmogenic 58 Severe Asthma 58 Non inferiority 58 BRCA2 gene 58 hyperprolactinemia 58 carotid IMT 58 Obstructive sleep apnea 58 HSCT 58 glycated hemoglobin levels 58 gestational diabetes mellitus 58 BRCA2 mutations 58 thyroglobulin 58 microRNA expression 58 APOE e4 gene 58 BRCA2 mutation carriers 58 recessive inheritance 58 pyloric stenosis 58 adrenal function 58 juvenile idiopathic arthritis 58 hemolytic anemia 58 cause cardiac channelopathies 58 advanced adenoma 58 cystatin C 58 stratifying patients 58 systolic hypertension 58 cardiac conduction 58 chronic granulomatous disease 58 hypoperfusion 58 prostate carcinogenesis 58 ruptured aneurysms 58 overt hypothyroidism 58 FASPS 58 HLA B# 58 nonalcoholic steatohepatitis NASH 58 FGFR2 gene 58 repolarization 58 tumor histology 58 bicuspid aortic valve 58 hepatorenal syndrome 58 thyroid nodules 58 gene variant 58 PSADT 58 mitochondrial diseases 58 Fragile X Syndrome 58 lichen planus 58 haemochromatosis 58 virological response 58 cerebral angiography 58 homozygous familial hypercholesterolemia 58 susceptibility gene 58 Cockayne syndrome 58 TCF#L# gene 58 HGPS 58 OSAHS 58 bronchopulmonary dysplasia BPD 58 carotid atherosclerosis 58 carcinoid tumor 58 T wave alternans 58 lethal arrhythmias 58 PTEN mutations 58 thrombocytopenic 58 ectodermal dysplasia 58 potentially modifiable 58 afib 58 chromosomal anomalies 58 hypokalemia hypomagnesemia 58 ataxias 58 vitamin B# deficiency 58 acute aortic dissection 58 ASDs 58 LRP5 58 D dimer 58 dopaminergic therapy 58 ischemic strokes 58 thoracic aortic aneurysm 58 pheochromocytoma 58 carcinoid tumors 58 ventricular arrhythmia 58 genetic variations 58 Recurrences 58 depressive symptomatology 58 CHD CVD 58 cardiac troponin 58 primary biliary cirrhosis 58 Obstructive Sleep Apnea 58 simplex virus 58 atypical ductal hyperplasia 58 Parkinson disease PD 58 BMPR2 58 white matter hyperintensities 58 p# mutations 58 mesotheliomas 58 ventricular tachyarrhythmia 58 hemodialysis patients 58 infective endocarditis 58 intracranial stenosis 58 carotid plaques 58 von Willebrand disease 58 chromosomal instability 58 pulmonary hypertension PH 58 IUGR 58 postoperative pulmonary 58 diffuse gastric 58 Autoimmune disorders 58 GBM tumors 58 multisystem disease 58 IDDM 58 TTTS 58 colorectal polyps 58 heterozygotes 58 malignant nodules 58 cortical dysplasia 58 Fragile X gene 58 cardio vascular disease 58 VaD 58 CTEPH 58 TGFBR1 * 6A 58 HCV infections 58 vascular dysfunction 58 inherited retinal degeneration 58 genetic variants 58 Gliomas 58 intestinal polyps 58 cardiac insufficiency 58 renovascular hypertension 58 fetal chromosomal 58 cardiac repolarization 58 atypia 57 enteroviral infection 57 SHPT 57 Lafora disease 57 endometrial cancers 57 preterm deliveries 57 PCNSL 57 prenatally diagnosed 57 neuropsychiatric disorder 57 bicuspid aortic valves 57 Alzheimer Disease AD 57 urolithiasis 57 atherosclerotic disease 57 Li Fraumeni syndrome 57 Polymorphic Ventricular Tachycardia CPVT 57 MYCN amplification 57 hepatic steatosis 57 tachyarrhythmias 57 latent TB infection 57 thrombotic complications 57 Sjögren syndrome 57 PTEN gene 57 fetal malformations 57 ductal adenocarcinoma 57 CHEK2 57 clinically insignificant 57 thyrotropin levels 57 Kufs disease 57 supratentorial 57 onset atrial fibrillation 57 C. trachomatis 57 polycystic ovary syndrome 57 neurodevelopmental outcome 57 Asymptomatic 57 trisomy 57 holoprosencephaly 57 sonographic diagnosis 57 artery stenosis 57 preeclampsia 57 Medulloblastoma 57 PTLD 57 azoospermia 57 Hypotension 57 VCUG 57 Hyperthyroidism 57 folate metabolism 57 UGT#A# * 57 cardiac hypertrophy 57 ischemic stroke 57 onset diabetes mellitus 57 essential thrombocythemia 57 BCR ABL mutations 57 inherited predisposition 57 bronchogenic carcinoma 57 AGHD 57 TT genotype 57 epithelial ovarian cancer 57 serum phosphate 57 deCODE BreastCancer TM 57 CMV infections 57 motor neuron degeneration 57 modifiable risk 57 genomewide 57 Fabry Disease 57 Cryptococcus neoformans 57 lactose malabsorption 57 poorer prognosis 57 Hypothyroidism 57 dopamine receptor gene 57 vascular cognitive impairment 57 Nonalcoholic Fatty Liver Disease 57 aneuploidy screening 57 neurocognitive impairment 57 nondiabetic 57 choriocarcinoma 57 Clusterin 57 monozygotic twin 57 hypoxemia 57 HeFH 57 mutated BRCA1 57 radioiodine therapy 57 congenital malformations 57 silent ischemia 57 GSTP1 57 QT prolongation 57 imatinib resistance 57 Chronic insomnia 57 Cognitive impairment 57 mammographic density 57 mitochondrial dysfunction 57 PALB2 57 onset Alzheimer disease 57 Moyamoya disease 57 valvular disease 57 N. gonorrhoeae 57 retrospective cohort 57 paraneoplastic 57 Irritable bowel syndrome IBS 57 Fanconi Anemia 57 carbohydrate intolerance 57 hereditary disorder 57 osteoporotic fracture 57 Meckel Gruber 57 intracranial hemorrhage ICH 57 transaminase levels 57 PsA 57 astrocytomas 57 homozygosity 57 BRCA1 BRCA2 57 Pulmonary arterial hypertension 57 histological subtype 57 Pre eclampsia 57 Coeliac disease 57 Wilms tumor 57 nonadherence 57 GH deficiency 57 neuro developmental disorder 57 warfarin dosing 57 IDH1 mutation 57 fructose intolerance 57 congenital anomaly 57 enterovirus infection 57 Testicular cancer 57 Alzheimer disease AD 57 CTAP# Capsules 57 gastric adenocarcinoma 57 perioperative complications 57 Glioblastoma Multiforme GBM 57 HER2 expression 57 neurofibromas 57 Kabuki syndrome 57 FXTAS 57 BRAF mutation 57 Ischemia 57 Glioma 57 Prostate Specific Antigen PSA 57 thromboembolic 57 penetrance 57 prolonged QT intervals 57 congenital hypothyroidism 57 DVT PE 57 Ankylosing spondylitis 57 Framingham Offspring Study 57 MTWA testing 57 allele frequencies 57 KIF6 gene 57 cranial irradiation 57 CCR5 delta# 57 ICD implantation 57 Flexi Scope 57 CIN3 57 chest radiographs 57 BRCA1 57 atherosclerotic lesions 57 CAG repeats 57 Thrombocytopenia 57 juvenile idiopathic arthritis JIA 57 gonococcal infection 57 primary immunodeficiency 57 mitochondrial mutations 57 folate deficiency 57 autistic traits 57 prediabetes 57 congenital adrenal hyperplasia CAH 57 herpes infection 57 Acute renal failure 57 Abdominal aortic aneurysms 57 multivariate logistic regression 57 leukocyte count 57 ANCA associated 57 malignant transformation 57 hyperkalemia 57 abnormal lipid 57 adenotonsillectomy 57 Major depressive disorder 57 fronto temporal dementia 57 Rectal cancer 57 nonhereditary 57 activating mutation 57 Parkinson Disease PD 57 GPC5 57 HGPIN 57 subarachnoid haemorrhage 57 neurologic symptoms 57 IPAH 57 DQB1 * 57 KRAS oncogene 57 medulloblastomas 57 TEAEs 57 subclinical 57 Framingham Offspring 57 VTEs 57 chronic rhinosinusitis 57 autosomal recessive 57 neurodevelopmental outcomes 57 TOMM# 57 nonobstructive CAD 57 Alport Syndrome 57 Critical limb ischemia 57 Leukemias 57 urine cytology 57 Barrett esophagus 57 cardiac abnormalities 57 congenital anomalies 57 inherited genetic mutation 57 MetS 57 diabetes mellitus T2DM 57 Lp PLA2 57 autoimmune thyroid 57 polyomavirus nephropathy 57 APOE 57 breast cancer metastasis 57 inherited neurodegenerative disorder 57 Arrhythmogenic Right Ventricular Cardiomyopathy 57 exhaled nitric oxide 57 genetic determinants 57 recurrent atrial fibrillation 57 Papillary 57 myeloid leukemia 57 hepatocellular carcinomas 57 cytogenic 57 genetic polymorphism 57 CHD7 57 neuroblastomas 57 Severe Primary IGFD 57 gene rearrangements 57 mutated K ras 57 ovarian hyperstimulation 57 etiologic 57 autoregulation 57 genetic variant 57 asymptomatic 57 Becker muscular dystrophy 57 Stent thrombosis 57 molecular abnormalities 57 spontaneous preterm delivery 57 fulminant hepatitis 57 breast carcinoma 57 NNRTI resistance 57 Retinoblastoma 57 lactate dehydrogenase LDH 57 stress cardiomyopathy 57 cytogenetic abnormalities 57 C. difficile colitis 57 herpesviruses 57 Chronic lymphocytic leukemia 57 optic neuropathy 57 chorioamnionitis 57 intracerebral haemorrhage 57 Candida infection 57 acute myelogenous leukemia AML 57 lactic acidosis 57 systemic scleroderma 57 invasive cervical cancer 57 neurodegenerative disorder 57 Observational studies 57 chromosomal anomaly 57 shorter telomeres 57 chronic myeloid 57 CA MRSA infections 57 giant cell arteritis 57 ICD shocks 57 psychiatric comorbidities 57 Marfan 57 highly heritable 57 chromosomal mutations 57 T2D 57 infantile hemangioma 57 untreated OSA 56 grade cervical intraepithelial 56 Unstable angina 56 Idiopathic pulmonary fibrosis 56 chronic hepatitis cirrhosis 56 colorectal cancer 56 neurologic sequelae 56 EXJADE 56 malignant pleural mesothelioma 56 beta blocker therapy 56 cerebral microbleeds 56 auditory neuropathy 56 relapsed ALL 56 Rh factor 56 arrhythmias 56 #F FDG PET 56 FMR1 56 recurrent seizures 56 AML MDS 56 chromosome abnormalities 56 causative gene 56 CYP #D# 56 hypermethylation 56 nonsense mutations 56 Niemann Pick disease 56 hematopoietic cancers 56 PIK3CA 56 genetic loci 56 troponins 56 angiographically 56 thyrotoxicosis 56 PAOD 56 hyper IgE syndrome 56 gene variation 56 hepatitis B infection 56 warfarin therapy 56 pCR 56 MTHFR 56 MLL2 56 impaired cognition 56 invasive meningococcal disease 56 estimated glomerular filtration 56 Leber Congenital Amaurosis LCA 56 Chronic HCV 56 status epilepticus 56 chromosome rearrangements 56 genetic mutations 56 androgen deficiency 56 thromboembolism 56 CNVs 56 LRAT 56 abnormal cytology 56 MDRD equation 56 esophageal adenocarcinoma 56 cervical carcinoma 56 anti JCV antibodies 56 presymptomatic 56 Hemophilia B 56 obstructive coronary artery 56 Cystatin C 56 Hydroxyurea 56 AA Amyloidosis 56 Myelodysplastic Syndrome 56 bivariate analysis 56 hemorrhagic complications 56 insulin resistance syndrome 56 venous thromboembolic disease 56 ApoE 56 Diabetic nephropathy 56 elevated serum ALT 56 MCADD 56 T1D 56 leptin deficiency 56 primary ciliary dyskinesia 56 MECP2 gene 56 differential gene expression 56 Latent TB 56 atrial fibrillation 56 JAK2 enzyme 56 lacunar 56 microalbumin 56 Alzheimers disease 56 dominantly inherited 56 myocardial infarctions MIs 56 neurologic deficits 56 Wernicke Korsakoff syndrome 56 fatal neurodegenerative disorder 56 MMSE scores 56 CYP#C# genotype 56 torsades de pointes 56 ventricular arrhythmias 56 QT interval 56 hematuria 56 albumin excretion rate 56 C#Y 56 metaplasia 56 MTWA 56 glomerular filtration rate 56 unruptured aneurysm 56 bicuspid valve 56 cryptogenic 56 diabetic nephropathy 56 fatty liver disease 56 familial aggregation 56 SNHL 56 chromosomal defects 56 KCNE2 56 normal karyotype 56 osteosarcomas 56 Hypertrophy 56 Malignant Melanoma 56 intracerebral hemorrhage 56 β blockers 56 arterial thickening 56 antibody mediated 56 neurodevelopmental disability 56 apolipoprotein E4 56 JAK mutations 56 Subarachnoid hemorrhage 56 pretransplant 56 mosaicism 56 mutation 56 pre eclamptic 56 chronic GVHD 56 spontaneous mutations 56 antenatal depression 56 COPD 56 spirometric 56 neurofibromatosis type 56 Acute Myeloid Leukaemia AML 56 Epstein Barr virus EBV 56 paroxysmal AF 56 undergoing radical prostatectomy 56 FGFR2 56 Trisomy 56 Long QT syndrome 56 euthyroid 56 atrial tachyarrhythmias 56 cryptorchidism 56 CYP#D# gene 56 thromboses 56 apolipoprotein E gene 56 mammary tumors 56 contrast induced nephropathy 56 airflow obstruction 56 methylation patterns 56 metastatic neuroendocrine tumors 56 serum lipid levels 56 hepatic toxicity 56 renal scarring 56 undergoing bariatric surgery 56 testicular tumors 56 Peripheral arterial disease 56 Hirschsprung disease 56 autoinflammatory diseases 56 dyslipidaemia 56 Fatty Liver Disease 56 abnormal Pap test 56 Cardiomyopathy 56 invasive breast cancer 56 polyp recurrence 56 G6PD 56 Myelodysplastic syndromes 56 myelofibrosis polycythemia vera 56 achromatopsia 56 channelopathies 56 antithrombotic therapy 56 BRAF V#E 56 cardiac troponin T 56 #q#.# [002] 56 intractable epilepsy 56 CMV disease 56 genetic defects 56 hypoglycaemic episodes 56 cardiac tamponade 56 KIF6 carriers 56 Chronic pancreatitis 56 homozygous FH 56 acute rheumatic fever 56 perioperative morbidity 56 hyperphenylalaninemia HPA due 56 galactosemia 56 gene variants 56 Estrogen Receptor 56 chromosomal disorder 56 sodium valproate 56 tuberculin skin testing 56 Endometrial cancer 56 premalignant 56 causative mutation 56 Sporadic CJD 56 Peripheral artery disease 56 deleterious mutation 56 SGPT 56 Hereditary angioedema HAE 56 ALT flares 56 leukocytosis 56 adenomas 56 hypercholesterolaemia 56 B7 H3 56 cerebral vasospasm 56 benign polyps 56 Li Fraumeni 56 p# activation 56 spontaneous mutation 56 Adenocarcinoma 56 colorectal bowel 56 alpha thalassemia 56 peripartum cardiomyopathy 56 S. aureus infection 56 reflux symptoms 56 tyrosine phosphorylation 56 nonsmall cell lung cancer 56 cTnT levels 56 Mild Cognitive Impairment 56 uncontrolled asthma 56 somatic mutation 56 chronic rhinosinusitis CRS 56 transient elastography 56 BRCA1 mutation carriers 56 Atrial fibrillation AF 56 molar pregnancy 56 albuminuria 56 somatic symptoms 56 levodopa therapy 56 ECG abnormalities 56 uterine tumors 56 careHPV 56 Gorlin syndrome 56 HCV antibody 56 leukemia ALL 56 chromosomal alterations 56 liver metastasis 56 Fluid retention 56 breast cancer genes BRCA1 56 macrovascular events 56 uveal melanoma 56 parkinsonian symptoms 56 NR#A# 56 Venous thromboembolism 56 promoter methylation 56 upper gastrointestinal bleeding 56 placental malaria