Related by context. All words. (Click for frequent words.) 61 apolipoprotein E4 59 APOE e4 59 KIF6 gene 59 defective telomerase 58 Genetic variation 58 APOC3 58 IgA deficiency 57 APOE gene 57 HFE gene 57 mtDNA mutations 56 FGFR2 56 shortened telomeres 56 C#Y 56 fetal chromosomal 56 humoral immunity 56 UGT#A# * 56 GABRA2 gene 56 APOE ε4 56 HbF 56 BDNF gene 56 chromosomal aberrations 56 TCF#L# gene 56 neuroD2 56 genes BRCA1 56 prostate carcinogenesis 56 CFTR gene 56 BRIP1 55 MC1R 55 ovarian hormones 55 CCR5 delta# 55 BRAF gene 55 MTHFR 55 CETP VV 55 STAT3 signaling 55 CYP#C# gene 55 MLL2 55 BARD1 55 APOE4 55 CALHM1 55 LPA gene 55 telomere lengths 55 APOL1 55 CNTNAP2 55 MSH2 55 autosomal dominant disorder 54 ApoE4 54 mitochondrial mutations 54 ENPP1 54 CDK4 54 C. neoformans 54 LRAT 54 MYH9 gene 54 transgene expression 54 MC4R gene 54 Fragile X gene 54 cardiac fibrosis 54 Genetic variants 54 autoimmune thyroid 54 SORL1 gene 54 LRP5 54 MC1R gene 54 nonsense mutation 54 APOE4 gene 54 APOE allele 54 HER2 overexpression 54 MECP2 gene 54 BRCA2 gene 54 PTPN# 54 HNPCC 54 gene APOE4 54 microvascular disease 54 Enlarged prostate 53 RPE# 53 nonischemic 53 BMPR2 53 nonsense mutations 53 estrogen deficiency 53 inherited mutations 53 gene variant 53 polycystic ovary syndrome PCOS 53 BRAF protein 53 Prolactin 53 C. pneumoniae 53 de novo mutations 53 KRAS oncogene 53 apoE4 53 RPE# gene 53 OPRM1 gene 53 STAT4 53 genes CYP#C# 53 dopamine receptor gene 53 variant alleles 53 mosaicism 53 ApoE4 gene 53 pituitary hormone 53 SHANK3 53 aneuploidy 53 Klotho gene 53 EGFR gene 53 cardioembolic stroke 53 motor neuron degeneration 53 Hair follicles 53 abnormal hemoglobin 53 SMN2 gene 53 intermittent hypoxia 53 Klinefelter syndrome 53 familial ALS 53 undergo apoptosis 53 heterozygotes 53 CNTNAP2 gene 53 ε4 53 GAB2 53 DRD2 gene 53 ADPKD 53 glutamate signaling 53 transgenic rats 53 TMEM#B 53 APOE e4 gene 53 RhD 53 extrapyramidal symptoms EPS 53 missense mutations 52 tumorigenicity 52 MHC genes 52 breast cancer genes BRCA1 52 CETP gene 52 epigenetic changes 52 androgen receptor gene 52 CP CPPS 52 MAOA gene 52 exfoliation glaucoma 52 Secondhand smoke exposure 52 male hormone androgen 52 SOD2 gene 52 HER2 gene 52 Helicobacter infection 52 CHRNA5 gene 52 apoC III 52 TACI mutations 52 sFlt 1 52 progressive neurodegenerative disorder 52 BCL6 protein 52 autonomic dysfunction 52 aneuploidies 52 PAOD 52 FMR1 gene 52 orofacial clefts 52 Parkinson disease neurodegenerative disorder 52 SCN5A 52 DISC1 gene 52 affective psychoses 52 prostate cancer CaP 52 G allele 52 Imprinted genes 52 Meckel Gruber 52 dopaminergic cells 52 CYP#D# gene 52 SORL1 52 FTO gene 52 leptin deficiency 52 growth hormone secretion 52 choroidal neovascularization CNV 52 HLA alleles 52 Hashimoto thyroiditis 52 elevated triglyceride levels 52 heritable variation 52 Bacterial vaginosis 52 colorectal tumor 52 RIP1 52 untreated hypothyroidism 52 SRBD 52 prolonged QT interval 52 LQTS 52 hypopituitarism 52 #q#.# [001] 52 cerebral ischemia 51 phthalate syndrome 51 HBeAg negative 51 follicle stimulating hormone FSH 51 PALB2 51 genetic variant 51 HPV subtypes 51 Plasmodium infection 51 severe congenital neutropenia 51 G6PD deficiency 51 testicular dysgenesis syndrome 51 neurologic complications 51 CCR5 mutation 51 familial pancreatic cancer 51 nephron 51 recessive mutation 51 GSTP1 51 testicular tumors 51 hypoperfusion 51 Genetic predisposition 51 rhinovirus infection 51 malperfusion 51 spermatogenesis 51 lung adenocarcinoma 51 androgen therapy 51 cystic fibrosis chronic pancreatitis 51 corpus luteum 51 neural tube defect 51 rs# [002] 51 transfusion syndrome 51 SOD1 gene 51 untreated celiac disease 51 androgen depletion 51 achromatopsia 51 anovulation 51 subfertility 51 NFKBIA 51 azoospermia 51 lysosomal enzyme iduronate 51 sickle hemoglobin 51 herpes zoster virus 51 chromosomal rearrangement 51 Chlamydia pneumoniae 51 nutlin 3a 51 desmin 51 inherited retinal degeneration 51 Hutchinson Gilford progeria 51 gene APOE 51 untreated OSA 51 Aortic stenosis 51 neurodevelopmental outcome 51 dopamine transporter gene 51 abnormal p# 51 Zinc deficiency 51 recurrent miscarriages 51 AAT deficiency 51 thyroid hormone levels 51 protein tyrosine phosphatase 51 GSTT1 51 TCF#L# 51 NPY gene 51 microcephalin 51 Premature menopause 51 Oxidative damage 51 recessive trait 51 somatic mutations 51 genetic variants associated 51 morphometric vertebral fractures 51 dystrophin gene 51 K ras mutations 51 Chronic insomnia 51 untreated sleep apnea 51 TGF beta signaling 51 dysglycemia 51 desmosomes 51 oxidant stress 51 GSTM1 51 CDKN2A 51 BRCA1 mutations 51 interferon pathway 51 androgen hormone 51 HPRT gene 51 PON1 gene 51 autoantibody 51 Mitral regurgitation 51 filaggrin gene 51 TEL AML1 50 primary ovarian insufficiency 50 renal flares 50 CFH gene 50 neovascularisation 50 chromosomal disorders 50 androgen excess 50 progranulin gene 50 HGPS 50 monogenic 50 sex hormones estrogen 50 adenovirus serotype 5 50 TRIM5a 50 parkinsonism 50 angina chest 50 polycystic ovarian syndrome PCOS 50 familial adenomatous polyposis 50 ventricular septum 50 5 HTT gene 50 SRY gene 50 thyroid dysfunction 50 intracranial hemorrhage ICH 50 inherited maternally 50 PD# [005] 50 varicoceles 50 pneumococci 50 GRNOPC1 cells 50 abnormal lipid 50 ApoE 50 PLX STROKE targeting 50 CIN2 + 50 placental function 50 ApoE gene 50 p# activation 50 MMP# 50 chromosomal defect 50 myelomeningocele 50 Arch Surg 50 gestational hypertension 50 Homozygous 50 LRRK2 gene 50 beta amyloid proteins 50 vesicular stomatitis virus 50 onset diabetes mellitus 50 arterial calcification 50 EBV infection 50 telomerase defects 50 metabolic dysfunction 50 shorter telomere length 50 asymptomatic PAD 50 V Leiden 50 female hormone estrogen 50 dopamine D4 receptor 50 tryptase 50 MYDICAR ® 50 hippocampal atrophy 50 T1DM 50 perioperative complications 50 SMN protein 50 IL#B 50 TCF4 50 recurrent VTE 50 fibrillin 1 50 VGN TZ# VGN TZ# 50 diabetic kidney 50 kainate 50 substantially improves treatability 50 kidney urologic 50 mutated K ras 50 lethal arrhythmias 50 oncogenic HPV 50 BRCA gene mutation 50 heterotaxy 50 Nf1 50 Stress hormones 50 MGUS 50 XMRV infection 50 ovulatory cycles 50 H. influenzae 50 amenorrhoea 50 missense mutation 50 microsatellite instability 50 abnormal lipid levels 50 Brugada syndrome 50 homozygotes 50 klotho gene 50 NOMID 50 severe periodontitis 50 heterozygous 50 Genetic mutations 50 chromosomal abnormalities 50 cytopathic 50 lupus scleroderma 50 inherited gene mutation 50 atherogenic dyslipidemia 50 CHD7 50 sex hormone estrogen 50 IUGR 50 dopaminergic therapy 50 airway hyperresponsiveness 49 MDR1 49 Critical limb ischemia 49 Malignant mesothelioma 49 unmeasured confounders 49 neuroblastoma tumors 49 STK# gene 49 CRISPR Cas 49 HER2 expression 49 arrhythmogenic 49 modifier genes 49 NOTCH1 49 HLA B# 49 CDH1 49 C#BL/#J 49 anthracycline induced 49 adeno associated viruses 49 mice genetically altered 49 anovulatory infertility 49 pDCs 49 chromosome #q# [002] 49 thrombocytopenic 49 Hemorrhagic stroke 49 fetal malformations 49 Akt signaling 49 transferrin saturation 49 CC genotype 49 NEIL1 49 pelvic prolapse 49 Myocardial infarction 49 alpha synuclein gene 49 Hip dysplasia 49 germline mutation 49 Eisenmenger syndrome 49 TNFAIP3 49 HLA genes 49 G#D mutation 49 squamous cell lung cancer 49 Hemorrhagic strokes 49 bacteria Streptococcus pneumoniae 49 gonadotropins 49 inherit predisposition 49 Prehypertension 49 nerve degeneration 49 BRCA2 gene mutation 49 huntingtin gene 49 immunodeficiencies 49 PTEN gene 49 headaches dizziness disorientation nausea 49 PTP1B 49 1 diabetes T1D 49 chlamydial infection 49 pathogenic mutations 49 urethritis 49 bronchopulmonary dysplasia 49 #q# deletion 49 chromosome abnormality 49 reproductive abnormalities 49 parasite Trypanosoma cruzi 49 Arrhythmogenic Right Ventricular Cardiomyopathy 49 microdeletions 49 multiple gestations 49 BRCA2 carriers 49 AML MDS 49 ovarian hyperstimulation 49 enterovirus infection 49 neurological sequelae 49 sexually dimorphic 49 Autoimmune disorders 49 HLA gene 49 clade B 49 F#del mutation 49 rotaviruses 49 narcolepsy cataplexy 49 dimorphic 49 prostate gland mammary gland 49 phenotypic expression 49 NF1 gene 49 da mage 49 hepatoma 49 familial hypercholesterolemia 49 undiagnosed celiac disease 49 recurrent miscarriage 49 vWD 49 Treg cell 49 GBM tumors 49 lung fibrosis 49 parainfluenza virus 49 Raynaud disease 49 intraoperative complications 49 CD8 cells 49 BRCA mutations 49 NNRTI resistance 49 hamartoma 49 advanced adenoma 49 gonadal 49 Chronic myeloid leukemia CML 49 capillary leakage 49 epistasis 49 APOE epsilon 4 49 germline mutations 49 leukemic transformation 49 murine leukemia virus 49 lymphatic vasculature 49 chronic granulomatous disease 49 folate metabolism 49 dentinal hypersensitivity 49 TGFBR1 49 lipid elevations 49 fibrotic disease 49 K#N 49 imprinted genes 49 HNSCC 49 adrenocortical cancer 49 severe rotavirus gastroenteritis 49 nonvertebral fracture 49 Lymphocytic 49 hyperparathyroidism 49 impaired cognition 49 beta adrenergic receptor 49 MGd 49 thoracic aortic disease 49 prion infection 49 autosomal recessive 49 Chronic pancreatitis 49 Vascular dementia 49 pyridostigmine 49 bronchial hyperresponsiveness 49 Pulmonary arterial hypertension 49 CCR3 49 APOE genotype 49 manganism 49 E4 variant 49 gestational diabetes mellitus GDM 49 SCD1 49 CCL#L# 49 genital abnormalities 49 experimentally induced 49 haptoglobin 49 FTO variant 48 atrophic gastritis 48 thrombotic complications 48 sexually transmitted HPV 48 PTEN tumor suppressor 48 penetrance 48 alkalosis 48 chronic GVHD 48 nonvaccine 48 genetic syndromes 48 Arch Intern Med 48 seropositive patients 48 sporadic ALS 48 orally administered synthetic retinoid 48 microdeletion 48 Heritability 48 CHEK2 48 Vitamin D insufficiency 48 cervical vulvar 48 dengue hemorrhagic fever DHF 48 PB1 F2 48 CMV infections 48 LV dysfunction 48 irreducibly complex 48 proliferative retinopathy 48 external genital lesions 48 Folate deficiency 48 apolipoprotein E gene 48 psychiatric comorbidity 48 congenital adrenal hyperplasia CAH 48 CYP#A# CYP#D# 48 PON1 48 mesotheliomas 48 pericardial mesothelioma 48 MTHFR gene 48 congenital disorders 48 tumor specific antigen 48 chimeric mice 48 hydrops 48 olfactory dysfunction 48 Tongue piercing 48 Thyroid hormone 48 genetically inherited 48 varicella infection 48 valvular heart disease 48 BRCA2 mutation carriers 48 potentially modifiable 48 genital lesions 48 Ets2 48 onset idiopathic hypogonadism 48 ricin Suey 48 female hormones estrogen 48 #q# deletion syndrome 48 developmental abnormalities 48 pre eclamptic 48 enteroviral infection 48 chromosomal instability 48 GATA4 48 Heterozygous 48 oligodendrogliomas 48 gastrointestinal stromal tumors GISTs 48 receiving immunosuppressive therapy 48 Male infertility 48 adenovirus vector 48 metabolic syndrome clustering 48 insertional mutagenesis 48 Premature Aging 48 KIBRA 48 TÎ ² 4 48 gastric carcinoma 48 holoprosencephaly 48 superinfection 48 inhaled allergens 48 CYP#A# gene 48 ANCA associated 48 Fetal heartbeats 48 number variations CNVs 48 reinterventions 48 impaired insulin secretion 48 Pulmonary hypertension 48 V#F 48 folic acid deficiency 48 ADH1B * 48 premature ovarian 48 DRD4 gene 48 cytomegalovirus CMV 48 Fatalistic kids 48 TTR gene 48 mucocutaneous reactions 48 polymorphic ventricular tachycardia 48 macroburst Ciemnecki 48 serum leptin 48 UGT#B# 48 FOXP2 gene 48 mammillary bodies 48 Dilated cardiomyopathy 48 innate immune 48 mutant genes 48 globin genes 48 colorectal neoplasia 48 receptor gene 48 bacterium Mycobacterium tuberculosis 48 Cockayne syndrome 48 extrapyramidal side 48 HER2 positive cancers 48 simian immunodeficiency virus 48 RSV infections 48 5q chromosome 48 infantile hemangioma 48 serum phosphate 48 rebleeding 48 medulloblastomas 48 Tasigna prolongs 48 chemokine receptor 48 K#R [002] 48 defective gene 48 male fathead minnow 48 persistent pulmonary hypertension 48 number variation CNV 48 stress hormone corticosterone 48 allele 48 Sexual dysfunction 48 vitamin B# deficiency 48 Kufs disease 48 inheritable genetic 48 Postherpetic neuralgia 48 testicular germ cell 48 TNF blocker therapy 48 gene variation 48 dioxin Zimpfer 48 ribosomal protein 48 cause cardiac channelopathies 48 superior mesenteric artery 48 skeletal muscle weakness 48 transgenic mouse models 48 hormone androgen 48 atherothrombotic disease 48 SHANK3 gene 48 BRCA mutation 48 malarial parasites 48 serum BDNF 48 susceptibility gene 48 familial AF 48 INTERHEART study 48 methylenetetrahydrofolate reductase 48 Ebstein anomaly 48 Sjögren syndrome 48 distal colon cancer 48 hereditary predisposition 48 suppressor gene 48 thrombus formation 48 aneuploid 48 corneal inflammation 48 PIGF 48 Tumor Necrosis Factor 48 ABCB1 48 RVOT 48 PROSTVAC VF 48 hormone imbalances 48 HbF levels 48 nonmelanoma skin cancers 48 Erythropoietic therapies may 48 ApoE4 allele 48 Wernicke Korsakoff syndrome 48 ALT flares 48 thiopurine 48 unmeasured factors 47 Nutritional deficiencies 47 Epstein Barr virus EBV 47 spontaneous preterm delivery 47 homozygous 47 systemic scleroderma 47 hypovitaminosis D 47 Chlamydia trachomatis 47 chromosomal imbalance 47 Ribavirin causes 47 airway narrowing 47 da maged 47 chronic hepatitis cirrhosis 47 abruption 47 nonvascular 47 genes BRCA 47 genetic imprinting 47 autosomal recessive disorder 47 M#V 47 esophageal squamous cell carcinoma 47 breast endometrial 47 chlamydial 47 germline cells 47 Genital herpes 47 vitamin B# folic acid 47 nonhereditary 47 dyskeratosis congenita 47 retinoid cycle 47 ovarian hyperstimulation syndrome OHSS 47 colorectal adenoma 47 previously uncharacterized 47 inhaled fibers 47 brassinosteroid 47 bacterial wilt disease 47 CYP #A# 47 abnormal Pap test 47 clefting 47 e4 allele 47 Degenerative disc disease 47 Postoperative complications 47 tardive dyskinesia TD 47 sexual dimorphism 47 hepatic toxicity 47 perfusion defects 47 BCR ABL protein 47 prion gene 47 thoracic aortic aneurysm 47 familial aggregation 47 Heavy menstrual bleeding 47 spinal misalignment 47 G#D 47 prematurity ROP 47 overt hepatic encephalopathy HE 47 Urinary tract 47 abnormal glucose metabolism 47 lowers homocysteine 47 DNA demethylation 47 obj obj = 47 Brugada Syndrome 47 adrenal suppression 47 hereditary hemochromatosis 47 Heavier loads 47 tricuspid atresia 47 maintaining cardiorespiratory fitness 47 FMRP protein 47 Uncontrolled hypertension 47 subclinical hyperthyroidism 47 receptor subunits 47 hereditary nonpolyposis colorectal cancer 47 genital defects 47 Peutz Jeghers syndrome 47 COL#A# 47 Acute Bacterial Sinusitis ABS 47 abnormal prions 47 rs# [004] 47 CMV infection 47 hereditary deafness 47 mammographic density 47 G#S mutation 47 obstructive coronary artery 47 Aortic aneurysms 47 atherothrombotic 47 chemoresistant 47 Asymptomatic 47 pyloric stenosis 47 dominantly inherited 47 oesophageal adenocarcinoma 47 mesothelial cells 47 congenital hypothyroidism 47 genital herpes infections 47 medulloblastoma tumors 47 pneumococcal infection 47 obstructive coronary 47 neurotransmitter norepinephrine 47 malarial infection 47 HBV infections 47 neurological abnormalities 47 DRD4 47 immunopathology 47 serotonin transporter gene 47 chronic bilirubin encephalopathy 47 unprotected vaginal 47 pAkt 47 poor metabolizers 47 DICER1 gene 47 ZNF# 47 Lupus nephritis 47 degenerative neurological diseases 47 pathologic myopia 47 HMGA2 gene 47 neurosensory 47 dyslipidaemia 47 HMPV 47 gene variants 47 corneal infection 47 p#INK#a 47 COMT gene 47 anal HPV 47 Mimail virus 47 bowel bladder 47 BRCA2 mutations 47 ESR1 47 hormone FSH 47 neuroendocrine 47 osteosarcomas 47 mutated genes 47 cancerdefine 47 BRCA1 BRCA2 47 VaD 47 AVODART 47 BLLs 47 primordial germ cells 47 Corolla Matrix vehicles 47 Erectile function 47 clade C 47 ventricular arrhythmia 47 mutant allele 47 slow metabolizers 47 progressive degeneration 47 Acute myeloid leukemia 47 Crown Crown Majesta 47 heritable genetic 47 neuropsychological impairments 47 symptomatic pulmonary embolism 47 autoantibody levels 47 lichen planus 47 Factor XIII 47 hepatitis B infection 47 chromosomal alterations 47 inherited neurodegenerative 47 retinal dystrophy 47 allelic variation 47 Cerebral malaria 47 bacterium Neisseria meningitidis 47 uterus fallopian tubes 47 HLA DRB1 47 Ischaemic heart 47 Epstein Barr Virus EBV 47 leptin resistance 47 inherited neurological disorder 47 residual confounding 47 alpha1 47 Salmonella typhi 47 perinatal asphyxia 47 sepsis infection Notaros 47 III EGFRvIII 47 bacteria Helicobacter pylori 47 Cowden syndrome 47 platelet dysfunction 47 NQO1 47 PrPSc 47 prospectively stratified 47 testosterone secretion 47 allelic variants 47 renal scarring 47 hormone aldosterone 47 physiological abnormalities 47 RTP# 47 tau gene 47 lymphangioleiomyomatosis LAM 47 perioperative morbidity 47 Myocardial perfusion 47 S. aureus colonization 47 MRAP variants 47 Soy isoflavones 47 acute aortic dissection 47 Neurofibromatosis type 47 congenital anomalies 47 placenta praevia 47 alpha1 antitrypsin deficiency 47 rhythm disturbances 47 synuclein 47 human herpesvirus 47 genetic defect 47 sinus node dysfunction 47 endoleaks 47 Pulmonary fibrosis 47 misregulation 47 FLT3 47 Thrombotic thromboembolic complications 47 TB germ 47 thrombosis blood clots 47 Sensorineural hearing loss 47 papillary renal cell carcinoma 47 Therein lurks 47 acute GVHD 47 homozygosity 47 Genetic mutation 47 SERT gene 47 vasogenic edema 47 postoperative delirium 46 beta thalassemia 46 2 diabetes T2D 46 hypoglycaemic episodes 46 tissue homeostasis 46 penile fibrosis 46 Polycystic ovary syndrome PCOS 46 penile anal 46 septal 46 immunological 46 underactive thyroid gland 46 anticholinergic drugs 46 opportunistic pathogens 46 abnormal angiogenesis 46 neurodegenerative disorder 46 atrial tachyarrhythmias 46 postoperative complication 46 Rh incompatibility 46 trivial Klatsky 46 autosomal 46 reproductive endocrine 46 Pelvic inflammatory 46 Alport Syndrome 46 pancreatic prostate 46 biochemical imbalances 46 hemorrhagic complications 46 Listeria infections 46 Plaque buildup 46 thyroid hormone deficiency 46 Cryptococcus neoformans 46 FADS2 gene 46 Severe hypoglycemia 46 recurrent glioblastoma multiforme 46 daytime drowsiness 46 endocrine glands 46 hardened arteries 46 QTc prolongation 46 5 HTTLPR 46 riociguat 46 careHPV 46 Difficulty swallowing 46 metabolizing enzyme 46 congenital abnormalities 46 mRNA transcripts 46 ependymoma 46 Wwox 46 amino acid substitutions 46 neurocognitive deficits 46 SCN1A 46 M.tb 46 ductal adenocarcinoma 46 Chronic sleep deprivation 46 Possessing Mistral 46 Joubert syndromes 46 coinfection 46 Proteostasis Network 46 S. enterica 46 genital HPV infections 46 prodynorphin 46 nondemented 46 embryonal rhabdomyosarcoma 46 TEP1 46 DQB1 * 46 habitat poaching 46 karyotype 46 scombroid poisoning 46 c KIT 46 subarachnoid hemorrhages 46 chromatin proteins 46 dysbindin gene 46 male reproductive organs 46 ovarian dysfunction 46 masculinisation 46 acute myocarditis 46 hepatitis C virus 46 neural progenitor 46 Hp2 2 46 disc herniations 46 Estrogen deficiency 46 multiorgan 46 discontinued Viread 46 Aflatoxin poisoning 46 hyperprolactinemia 46 hormone estradiol 46 juvenile idiopathic arthritis JIA 46 BRAF mutation 46 Vangl2 46 carotid atherosclerosis 46 Articular cartilage 46 GH deficiency 46 metastatic lung cancer 46 diabetes mellitus DM 46 OPRM1 46 Leishmania parasite 46 postoperative hemorrhage 46 Alu elements 46 HLA DQ2 46 syngeneic 46 outcrossing 46 KRAS wild 46 myopathies 46 aortic rupture 46 Idiopathic pulmonary fibrosis IPF 46 multisystem disease 46 Growler electronic 46 intensive statin therapy 46 defective cilia 46 oestrogens 46 mitral stenosis 46 simplex virus 46 vaccinees 46 systemic lupus erythematosus SLE 46 driver airbag inflator 46 Diabetic neuropathy 46 autosomal recessive disease 46 immunodeficiency 46 chronic HBV infection 46 protein neuraminidase 46 microchimerism 46 USI hereafter becomes 46 outflow tract 46 HBeAg positive 46 myalgic encephalomyelitis ME 46 genital ulcer 46 Plasmodium falciparum