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(Click for frequent words.) 73 predisposes 67 predisposing 63 genetic predisposition 59 genetically predisposed 58 susceptibility 58 predisposed 57 genetically susceptible 56 predisposition 56 predisposing factor 56 metabolic abnormalities 55 genetic susceptibility 55 hereditary predisposition 54 predisposing factors 54 genetically inherited 54 Genetic predisposition 53 genes predisposing 53 prothrombotic 53 metabolic disturbances 52 causally linked 52 insulin resistance 52 PTEN mutations 52 genetic predispositions 52 dysregulated 52 metabolic abnormality 52 shorter telomere length 51 mental retardation epilepsy 51 inherited predisposition 51 biological predisposition 51 causal pathway 50 susceptibility genes 50 highly heritable 50 MYH9 gene 50 diabetes cardiovascular disease 50 genes predispose 50 AUDs 50 potentially modifiable 50 impaired cognition 50 act synergistically 50 chronicity 50 susceptibility gene 50 e4 allele 50 systemic inflammation 50 dominantly inherited 49 atopic disorders 49 pathogenesis 49 underlying pathophysiology 49 susceptible 49 neuronal dysfunction 49 obesity insulin resistance 49 familial clustering 49 osteopenia osteoporosis 49 underactive thyroid gland 49 lethargy irritability 49 root caries 49 ovarian dysfunction 49 aggravate respiratory 49 chromosomal regions 49 lupus scleroderma 49 hormones neurotransmitters 49 autosomal recessive 49 biologically predisposed 49 dyslipidemia hypertension 49 paralysis coma 49 allergic sensitization 49 genetic trait 49 hypertension diabetes mellitus 49 genetic mutations 49 inherited mutations 49 untreated celiac disease 48 maintaining cardiorespiratory fitness 48 cerebral palsy multiple sclerosis 48 genetic determinants 48 hyperinsulinemia 48 thyroid hormone levels 48 overactivated 48 Genetic variations 48 GABRA2 gene 48 neurological abnormalities 48 carotid atherosclerosis 48 arthritis osteoporosis 48 menstrual irregularity 48 Genetic variants 48 Fragile X gene 48 structural abnormalities 48 Hip dysplasia 48 modifiable risk 48 LRRK2 mutations 48 abnormal methylation 48 arthritis gout 48 PTPN# 48 germline mutations 48 microdeletion 48 insulin resistance syndrome 48 dopamine D2 receptors 48 coinfection 48 heritable 48 hippocampal function 48 cystic fibrosis sickle cell 48 rheumatoid arthritis lupus 48 associated tremor ataxia 48 hypertension cardiovascular disease 48 HFE gene 48 autonomic nerve 48 hypokalemia hypomagnesemia 48 developmental abnormalities 48 Erythropoietic therapies may 48 embryonic tissues 48 misregulation 48 circulating estrogens 48 narcolepsy cataplexy 48 genetic polymorphism 48 TNFAIP3 48 abnormal vaginal bleeding 48 undescended testicles 48 microvascular disease 48 multifactorial 48 familial polyposis 48 inhibit 48 PON1 48 neurological disorder characterized 48 familial hypercholesterolemia FH 47 congenital deficiency 47 causative factor 47 gene predisposing 47 leptin deficiency 47 Hormonal imbalances 47 mitochondrial mutations 47 gestational diabetes mellitus 47 causally related 47 hormonal abnormalities 47 Bardet Biedl Syndrome 47 endocrine abnormalities 47 impaired glucose metabolism 47 overactivity 47 GRK5 47 Untreated sleep apnea 47 cervicitis 47 cardiovascular disease osteoporosis 47 disorder characterized 47 apolipoprotein E4 47 MTHFD1L gene 47 asthma bronchitis emphysema 47 autoimmune thyroid 47 genetic variant 47 metabolic dysfunction 47 Cowden syndrome 47 immune dysregulation 47 epigenetic changes 47 vascular constriction 47 APOE4 47 psychologic 47 motor neuron degeneration 47 dopamine receptor gene 47 diabetes dyslipidemia 47 DQB1 * 47 genetic variants 47 inflammatory bowel syndrome 47 G allele 47 neurodevelopmental 47 breast endometrial 47 maladaptive 47 cardiometabolic disorders 47 genetically predetermined 47 Colon polyps 47 Modifiable risk 47 Left untreated 47 gene variant 47 neuropsychiatric disorders 47 both genders chromosomal 47 phenotypes 47 researchers hypothesized 47 susceptibility locus 47 ADH1B 46 Androgenetic alopecia 46 gene variants 46 painful menstrual periods 46 gene locus 46 reproductive abnormalities 46 epigenetic modification 46 poorer prognosis 46 BARD1 46 diathesis 46 heritable disorders 46 HGPS 46 abnormal lipids 46 Vitamin B# deficiency 46 unwanted pregnancies sexually transmitted 46 syndrome FXTAS 46 abnormal lipid levels 46 strongest predictors 46 Psychotropic medications 46 polyglutamine diseases 46 Heredity 46 gastrointestinal disturbances 46 allergic eczema 46 sickle cell cystic fibrosis 46 coronary microvascular 46 apolipoprotein E gene 46 cystic ovaries 46 familial adenomatous polyposis 46 APOE gene 46 chromosomal disorders 46 muscular dystrophy cystic fibrosis 46 hypothalamic amenorrhea 46 TMEM#B 46 gastric carcinogenesis 46 penetrance 46 recessive genetic 46 genetic polymorphisms 46 Excessive daytime sleepiness 46 hypothesized 46 Li Fraumeni syndrome 46 teratogens 46 hypercoagulability 46 polygenic 46 dysregulation 46 osteoporosis osteopenia 46 myopathies 46 elevated triglycerides 46 urethritis 46 pathophysiologic 46 osteochondrosis 46 chromosomal rearrangement 46 childhood disintegrative disorder 46 bone deformities 46 Genetic mutations 46 periodontal infections 46 metabolic syndrome 46 Maternal obesity 46 progranulin mutations 46 atherosclerosis 46 hypoactive 46 excitotoxic 46 activity MAOA 46 vascular dysfunction 46 fat malabsorption 46 glaucoma ischemia 46 puerperal psychosis 46 nonhereditary 46 hypoxic ischemic brain 46 etiology 46 cardiac fibrosis 46 arteriosclerotic 46 degenerative neurological diseases 46 C. pneumoniae 46 atherosclerotic cardiovascular 46 leaky gut 46 functional polymorphism 46 phenotype 46 nonalcoholic steatohepatitis 46 left ventricular hypertrophy 46 asthma allergies 46 biochemical imbalances 46 hormonal disturbances 46 neurologic disorders 46 CYP#D# gene 46 hepatic renal 46 #q#.# [002] 46 hereditary hemochromatosis 46 elevated prolactin 46 mutant huntingtin protein 46 torsade de pointes 46 antiphospholipid syndrome 46 primary ovarian insufficiency 46 premalignant 46 regulate gene expression 46 CFH gene 46 serine proteases 46 infertility miscarriage 46 neurohormones 46 neuroligins 46 hemoglobinopathies 46 neurobiological 45 chromosomal anomalies 45 basal cell nevus syndrome 45 CHD7 45 osteomalacia 45 severe obstructive pulmonary 45 impulsive behaviors 45 atherosclerosis hardening 45 hormonal imbalances 45 APOE4 variant 45 inflammatory bowel 45 Oxidative stress 45 folate deficiency 45 hypertension hypercholesterolemia 45 prolonged immobilization 45 pathophysiology 45 LIS1 45 genetically disposed 45 dilated veins 45 hypoxia inducible 45 multiple sclerosis cerebral palsy 45 parkinsonian 45 untreated hypothyroidism 45 immuno suppressed 45 APOE genotype 45 familial predisposition 45 researchers hypothesize 45 clefting 45 arteries harden 45 MAOA gene 45 inherit predisposition 45 frequent bowel movements 45 obstructive coronary 45 congenital abnormalities 45 impair fertility 45 genetically programmed 45 molecular underpinnings 45 neuroinflammation 45 MTHFR 45 atopic asthma 45 estrogen metabolism 45 airway reactivity 45 obesity sedentary lifestyle 45 vascular Ehlers Danlos 45 upregulates 45 NRF2 gene 45 biologic pathways 45 Meckel Gruber 45 untreated sleep apnea 45 FGFs 45 hereditary nonpolyposis colorectal cancer 45 D3 receptors 45 aetiological 45 asplenia 45 tremor slowness 45 fever dehydration 45 dendritic spine 45 proinflammatory 45 Prenatal exposure 45 chorioamnionitis 45 comorbid disorders 45 coma convulsions 45 masculinizing 45 OPRM1 gene 45 disorder Ketchmark 45 lipoprotein metabolism 45 heritable genetic 45 amyloid plaque formation 45 cardio metabolic 45 dysthymic 45 neuro degenerative disorders 45 subclinical 45 psychosocial stressors 45 gastro oesophageal reflux 45 arthritis lupus 45 familial pancreatic cancer 45 BRCA2 breast cancer 45 immunodeficiencies 45 DRD4 gene 45 adiponectin levels 45 eczema asthma 45 lordosis 45 endothelial dysfunction 45 cardiomyopathies 45 intestinal disorders 45 metabolic alterations 45 predispositions 45 germline mutation 45 gene mutations 45 FXTAS 45 epilepsy cerebral palsy 45 induces 45 dizziness nausea headaches 45 eczema hay fever 45 repetitive stereotyped 45 APOE ε4 45 overactive thyroid gland 45 lupus rheumatoid arthritis 45 ichthyosis vulgaris 45 activate p# 45 autoimmune thyroiditis 45 V Leiden 45 Myotonic dystrophy 45 nicotinic receptor 45 insulin resistant 45 progressive neurologic 45 inattention drowsiness 45 hereditary nonpolyposis colon cancer 45 genus Plasmodium 45 ataxias 45 inverse agonist 45 epilepsy Parkinson disease 45 autism dyslexia 45 HLA DRB1 * 45 attenuates 45 compensatory mechanisms 45 Nasal polyps 45 Hashimoto thyroiditis 45 persistent pulmonary hypertension 45 TMJ temporomandibular joint 45 emphysema chronic bronchitis 45 inflammatory markers 45 asthma rhinitis 45 comorbid psychiatric 45 mitochondrial metabolism 45 cardiovascular disease hypertension 45 muscular spasticity 45 modifiable cardiovascular 45 chromosomal translocations 45 prenatally exposed 45 COMT gene 45 nongenetic 45 depression irritability 45 lipid metabolism 45 autonomic dysfunction 45 Fatty liver 45 chromosomal alterations 45 neuritic 45 apoC III 45 skeletal muscle weakness 45 unexplained vaginal bleeding 45 pathophysiological mechanisms 45 glucose intolerance 45 Yolken 45 comorbid anxiety 45 parkinsonism 45 SCA5 45 testicular tumors 45 Viral infections 45 allele 45 alexithymia 45 shorter telomeres 45 Hormonal imbalance 45 inherited neurodegenerative 45 use disorders AUDs 45 SE alleles 45 colic diarrhea 45 Heterozygous 45 induce 45 metabolizing enzymes 45 fatty liver disease 45 hay fever asthma 45 GABRA2 45 blindness amputation 45 Arrhythmogenic Right Ventricular Cardiomyopathy 45 neurological degeneration 45 Genetic variation 45 Subclinical 45 aldehyde dehydrogenase 45 hyperinsulinemic 45 etiologic factors 45 APOE e4 45 menarche 45 Dysregulation 45 atherosclerosis plaque buildup 45 levodopa induced 45 Malassezia 45 etiologic 45 causative gene 45 #q# deletion 45 desmin 45 inhibitory neurotransmitters 45 epilepsy multiple sclerosis 45 hypothalamic pituitary 44 ε4 44 cause cardiac channelopathies 44 post transplant lymphoproliferative 44 abnormal genital 44 SIADH 44 STAT4 44 heritable component 44 prostate carcinogenesis 44 Hypertrophic cardiomyopathy 44 G6PD deficiency 44 upregulate 44 anatomical abnormalities 44 granulosa cell 44 gastric atrophy 44 Chlamydia pneumoniae 44 virulence genes 44 metabolic syndromes 44 abdominal pain vomiting 44 COPD asthma 44 Iron deficiency 44 metabolic disorders 44 genetic variations 44 congenital anomalies 44 Magnesium deficiency 44 Gleevec inhibits 44 INF2 44 genetic defect 44 Dilated cardiomyopathy 44 premutation 44 subclinical hyperthyroidism 44 nerve degeneration 44 Insulin resistance 44 autoimmune disorder characterized 44 progressive neurodegenerative 44 Compulsive hoarding 44 adiposity 44 elevated CRP 44 arterial calcification 44 spina bifida cerebral palsy 44 polymorphisms 44 BMPR2 44 normal karyotype 44 metabolic 44 Chronic pancreatitis 44 Pseudomonas syringae 44 genes 44 collagen vascular 44 abnormal lipid 44 renal fibrosis 44 nucleus Chinnery 44 BRCA1 BRCA2 44 Tay Sachs thalassemia 44 stimulate insulin secretion 44 blood clotting disorders 44 Nausea vomiting 44 causes stomach ulcers 44 polycystic ovarian disease 44 genomic instability 44 IL#R 44 GSTT1 44 Thyroid hormone 44 filaggrin gene 44 remnant lipoproteins 44 Thrombotic thromboembolic complications 44 androgen deficiency 44 polycystic ovary 44 underlie 44 syndromes 44 dopamine transporter gene 44 experimentally induced 44 CETP gene 44 TRPV1 receptors 44 uric acid stones 44 Hyperthyroidism 44 missense mutations 44 fibromyalgia lupus 44 behavioral disinhibition 44 Zinc deficiency 44 neuroendocrine 44 muscles tendons ligaments 44 chronic bronchitis emphysema 44 hormone aldosterone 44 thrombophilia 44 onset puberty 44 UGT#B# 44 developmental trajectories 44 obstructive pulmonary disease 44 lipid concentrations 44 psychiatric comorbidity 44 Klinefelter syndrome 44 anxiety suspiciousness 44 airway hyperresponsiveness 44 meningitis encephalitis 44 osteoporosis arthritis 44 genetic susceptibilities 44 muscular stiffness 44 APOE4 gene 44 endocannabinoid signaling 44 psychopathological disorders 44 chromosomal anomaly 44 infertility ectopic pregnancy 44 neurodevelopment 44 cystic fibrosis Duchenne muscular 44 alpha synuclein protein 44 gene mutation 44 nausea vomiting rash 44 tremors convulsions 44 KIBRA 44 prenatal testosterone 44 pleiotropic 44 alpha synuclein gene 44 Apolipoprotein E4 44 ARID1A 44 channelopathies 44 periodontal infection 44 TNF blocker therapy 44 aggravate 44 growth hormone secretion 44 maternally transmitted 44 cognitive deficits 44 neurogenic 44 gut microbiota 44 premature ovarian 44 activate AMPK 44 LPA gene 44 motor neuron diseases 44 hyper excitability 44 estrogenic effects 44 prostate pancreatic 44 clog arteries 44 MYH9 44 dysplastic lesions caused 44 unhealthier lifestyles 44 M. catarrhalis 44 central adiposity 44 osteoporosis brittle bones 44 P. ovale 44 Porphyromonas gingivalis 44 irregular menstrual cycles 44 Radiographic findings 44 rheumatoid arthritis inflammatory bowel 44 carotid plaques 44 Exertional 44 metabolic syndrome cluster 44 non syndromic 44 disc degeneration 44 Gestational 44 exacerbate 44 coinfections 44 PLMs 44 neurotransmission 44 authors conclude 44 granulomatous 44 gut microbes 44 cirrhotic liver 44 Inflammatory bowel diseases 44 Gastroesophageal reflux disease 44 epididymitis 44 neuropsychological deficits 44 genetic makeups 44 neurocognitive dysfunction 44 disable virulence 44 MAOA 44 causes genital warts 44 socially stigmatized 44 estrogen deficiency 44 Dr. Ivashkiv 44 degenerative neurological 44 abdominal adiposity 44 renin angiotensin system 44 chronic hepatitis cirrhosis 44 mental retardation blindness 44 untreated obstructive sleep 44 atopy 44 cystic fibrosis muscular dystrophy 44 variable ptau levels 44 ligament laxity 44 neurobehavioral symptoms 44 rheumatoid 44 genetic alterations 44 hormonally sensitive 44 Impulsivity 44 VLDL cholesterol 44 interferon pathway 44 subclinical infection 44 hormone secretion 44 Howard Sesso 44 inborn 43 FGFR2 gene 43 spongiform encephalopathies 43 serotonin transporter 43 aggravate allergies 43 autosomal dominant 43 induced cardiomyopathy 43 hypertensive retinopathy 43 ABCB1 gene 43 causes bloody diarrhea 43 multiple sclerosis rheumatoid arthritis 43 ABCB1 43 ego dystonic 43 trophoblastic 43 epigenetic regulation 43 vascular inflammation 43 neoplastic 43 multifactorial disease 43 Kufs disease 43 cerebral palsy spina bifida 43 sonographic appearance 43 paraneoplastic 43 clinically heterogeneous 43 chromosomal instability 43 MC1R 43 Parkinsonian 43 thyrotropin levels 43 nonalcoholic steatohepatitis NASH 43 improves insulin sensitivity 43 muscular dystrophies 43 acetabular dysplasia 43 primary ciliary dyskinesia 43 Susceptibility 43 electrolyte abnormalities 43 candida albicans 43 causative 43 male hormone androgen 43 cognitive dysfunctions 43 inheritable 43 multi factorial disease 43 hypoxemia 43 gene APOE 43 prefrontal regions 43 causative genes 43 dissecans 43 tremors numbness 43 immunomodulatory effects 43 alpha1 43 skeletal malformations 43 promoter polymorphism 43 hyperinsulinism 43 psychotic illnesses 43 syndrome OSAS 43 constipation bloating 43 amputations blindness 43 Antisocial personality 43 Muscle cramps 43 heterotaxy 43 MHC genes 43 Bacterial vaginosis 43 cortical thinning 43 obstructive sleep apnea hypopnea 43 oxidized phospholipids 43 Oxidative 43 hypercoagulable 43 coronary artery atherosclerosis 43 ApoE4 gene 43 neurobiological basis 43 Evolutionarily speaking 43 insertional 43 circadian rhythm disorders 43 autosomal recessive disease 43 hypercalciuria 43 breast cancer genes BRCA1 43 Sleep disturbances 43 spastic paraplegia 43 deafness meningitis 43 pituitary tumors 43 hyperhomocysteinemia 43 underactive 43 afflict 43 carbohydrate intolerance 43 EP3 receptor 43 Thyroid gland 43 polyglutamine 43 pathophysiological 43 Lesch Nyhan syndrome 43 Comorbid 43 atherosclerotic coronary 43 Neurodegenerative disorders 43 genetic loci 43 cystic fibrosis chronic pancreatitis 43 allergic dermatitis 43 hyperresponsiveness 43 fatigue dizziness 43 mammary cancers 43 Breastfed infants 43 matriptase 43 serum BDNF 43 inversely associated 43 recessive trait 43 metabolize alcohol 43 shorten telomeres 43 Wernicke Korsakoff syndrome 43 SLC#A# gene [002] 43 CIB1 43 Hormonal changes 43 nonalcoholic fatty liver 43 neurodegenerative disorder characterized 43 meningitis encephalitis pulmonary edema 43 atopic 43 monogenic 43 normal gut flora 43 metabolizing enzyme 43 APOE epsilon 4 43 behavioral abnormalities 43 chromosomal deletions 43 Von Willebrand disease 43 misperceive 43 Calcium vitamin D 43 lymphomas leukemias 43 prone 43 fibrocystic 43 BRCA2 gene 43 phenothiazines 43 genetic mutation 43 TMPRSS6 43 pancreas pancreatitis 43 impair cognition 43 dysplasias 43 induce insulin resistance 43 mutations 43 Pulmonary hypertension 43 hyperparathyroidism 43 Vitamin D insufficiency 43 Oxidative damage 43 thyroid dysfunction 43 testicular germ cell 43 related maculopathy 43 comorbid depression 43 advanced glycation endproducts 43 eccrine 43 multiple sclerosis inflammatory bowel 43 disease NAFLD 43 regulates gene expression 43 fibromyalgia arthritis 43 heritable diseases 43 mucus glands 43 Secondhand smoke exposure 43 apolipoprotein E 43 inhale vomit 43 electrolyte imbalances 43 abnormalities 43 unstable detrusor muscle 43 MTP inhibitor 43 TSC1 43 cirrhosis liver failure 43 systemic autoimmune 43 menstrual irregularities 43 irregular menstrual periods 43 #q#.# [001] 43 de novo mutations 43 MLH1 43 thrombo embolic 43 GABA aminotransferase 43 chromosome #q# [001] 43 Chronic inflammation 43 immunocompromised individuals 43 gastric carcinoma 43 CAG repeats 43 Irritability anxiety cognitive 43 cartilage tendons 43 inhaled allergens 43 TP# mutation 43 C#Y 43 GAB2 43 Apolipoprotein E 43 Disrupted sleep 43 Researchers hypothesize 43 schizophreniform 43 cardiopulmonary diseases 43 p# mutations 43 neuropsychiatric diseases 43 neuro degenerative 43 amyloidogenic 43 subclinical disease 43 neuroinflammatory 43 hyperreflexia 43 Lactose intolerance 43 utero exposure 43 diabetic microvascular complications 43 PPARg 43 bronchitis emphysema 43 APOE e4 allele 43 hypothalamic pituitary adrenal axis 43 Peripheral artery 43 irritative 43 nervousness irritability 43 Tasigna prolongs 43 melanocortin receptor 43 polymicrobial 43 neurohormonal 43 genital tract 43 Korsakoff syndrome 43 Hereditary angioedema 43 tooth decay gum 43 metabolize cholesterol 43 Myostatin 43 leptin resistant 43 chronic rheumatic 43 convulsive disorders 43 moderately heritable 43 aggravate asthma 43 endogenous opioid 43 ischemic vascular 43 venous thrombosis 43 Atopic dermatitis 43 LDLs 43 genetic underpinnings 43 Angiotensin II 43 SHANK3 gene 43 XMRV infection 43 ovarian hormones 43 CDH1 43 Raynaud syndrome 43 pituitary hormone 43 Frontal lobe 43 lightheadedness fainting 43 precancerous cervical 43 blindness paralysis 43 multiple sclerosis psoriasis 43 epigenetic markers 43 atypical moles 43 oral thrush 43 endophenotypes 43 progressive dyspnea 43 COL#A# 43 multiple sclerosis muscular dystrophy 43 connective tissue disorders 43 NSAID associated 43 Yeast infections 43 darker pigmentation 43 inflammatory bowel disease 43 joints tendons 43 underdiagnosed 43 abcesses 43 orthostatic hypotension cataracts 43 intraventricular hemorrhage 43 anatomic abnormalities 43 upper airway 43 dermatologic reactions 43 palmitoylation 43 Idiopathic 43 carbohydrate metabolism 43 unhealthy dietary habits 43 circadian rhythm sleep 43 genetic variants associated 43 evolutionarily novel 43 serotonin receptor 43 asthma eczema 43 apoE 43 mGluR 43 wheezing breathlessness 43 insomnia dizziness 43 CYP#E# gene 43 myocardial infarction congestive heart 43 rheumatoid arthritis multiple sclerosis 43 Mitral valve 43 serotonin signaling 43 galanin 43 ORMDL3 43 mitochondrial abnormalities 42 chronic degenerative diseases 42 Bullous 42 hydrops 42 mammograms Hruska 42 Alzheimer pathology 42 ventricular hypertrophy 42 Degenerative diseases 42 Neurofibromatosis type 42 Dr. Gozal 42 causal pathways 42 Overfeeding 42 cell adhesion molecules 42 mitochondrial dysfunction 42 urogenital 42 spontaneous mutations 42 Stress hormones 42 cells secrete 42 molecular mechanisms underlying 42 Barrett esophagus BE 42 encephalitis meningitis 42 neurologic disorder 42 enlarged glands 42 menstrual dysfunction 42 hives itching 42 Rh incompatibility 42 tinnitus vertigo 42 P. aeruginosa infection 42 Calcification 42 PTEN gene 42 SIRT3 42 SLC#A# [002] 42 COX enzymes 42 genital ulcer 42 aetiology 42 nonischemic 42 5 HT1A receptor 42 upper airway obstruction 42 congenital disorders 42 antisocial traits 42 abdominally obese 42 hypertrophic cardiomyopathy HCM 42 serotonin norepinephrine 42 dyslipidemias 42 podocyte 42 precancerous tumors 42 thyroid hormone deficiency 42 polydipsia 42 mal absorption 42 maternally derived 42 abnormal blood clotting 42 hallux valgus 42 confer susceptibility 42 #q# [001] 42 sleep apnea narcolepsy 42 Susan B. Shurin 42 polyhydramnios 42 NSAID induced GI 42 Karayiorgou 42 recessive inheritance 42 cardiac hypertrophy 42 spontaneously abort 42 bacterial parasitic 42 PLX STROKE targeting 42 folic acid deficiency 42 Menkes disease 42 TCF#L# gene 42 antiphospholipid antibodies 42 blindness deafness mental retardation 42 heterozygous familial 42 galactosemia 42 neuromotor 42 synaptogenesis 42 airway hyperreactivity 42 commonest cause 42 Pelvic inflammatory 42 orexin receptors 42 heterozygous 42 neurofibrillary 42 asymptomatic bacteriuria 42 irritability mood swings 42 breast carcinogenesis 42 hypogonadotropic hypogonadism 42 nicotine receptor 42 recurrent wheezing