Related by context. All words. (Click for frequent words.) 65 autoinflammatory diseases 65 pathogenic mechanisms 65 Genetic variants 64 protein misfolding diseases 64 inherited retinal degeneration 64 neuropsychiatric diseases 64 Irritable bowel syndrome IBS 64 ataxias 63 molecular abnormalities 63 Autoimmune disorders 63 myelofibrosis polycythemia vera 63 TTR amyloidosis 63 monogenic 63 neuropsychiatric disorder 62 biologic pathways 62 motor neuron diseases 62 degenerative neurological diseases 62 demyelinating diseases 62 Prion diseases 62 DNA methylation patterns 62 Atopic dermatitis 62 ANCA associated 62 Parkinsonian Syndromes 62 muscular dystrophies 62 Myotonic dystrophy 62 systemic autoimmune 61 obesity insulin resistance 61 underlying pathophysiology 61 inflammatory demyelinating 61 Aortic stenosis 61 Neurodegenerative diseases 61 Eisenmenger syndrome 61 inflammatory bowel diseases 61 lysosomal storage diseases 61 sporadic ALS 61 hereditary predisposition 61 causative genes 61 childhood disintegrative disorder 61 clefting 61 neuro degenerative disorders 61 genetic syndromes 61 lipid disorders 61 inherited neurological disorder 61 metabolic abnormalities 61 respiratory gastrointestinal 61 biologic pathway 61 blood coagulation disorders 61 familial pancreatic cancer 60 temporal arteritis 60 respiratory viral infections 60 FTLD 60 Eosinophilic esophagitis 60 Hutchinson Gilford progeria 60 airway hyperresponsiveness 60 cortical dysplasia 60 dominantly inherited 60 neurogenetic 60 mitochondrial disorders 60 Chronic insomnia 60 hereditary spastic paraplegia 60 neuroinflammation 60 neurodegenerative disorder 60 PTEN mutations 60 Irritable bowel syndrome 60 protein tyrosine phosphatases 60 narcolepsy cataplexy 60 Shy Drager syndrome 60 Neurological disorders 60 Sleep disordered breathing 60 de novo mutations 60 multisystem disease 60 Myasthenia gravis 60 Tay Sachs thalassemia 60 Von Willebrand disease 60 Mood disorders 60 syndromic 60 Systemic lupus erythematosus 60 kidney urologic 60 mtDNA mutations 60 lupus multiple sclerosis 59 neuropsychiatric disorders 59 Autoimmune diseases 59 nonbacterial prostatitis 59 biochemical imbalances 59 Chronic sinusitis 59 G6PD deficiency 59 GI motility disorders 59 emotional dysregulation 59 chromosomal rearrangement 59 neuro developmental disorder 59 CNTNAP2 59 MYH9 gene 59 cystic fibrosis chronic pancreatitis 59 neuropathies 59 prostate carcinogenesis 59 Psoriatic arthritis 59 autism Asperger 59 Cryptococcus neoformans 59 neurobehavioral disorder 59 Inflammatory bowel diseases 59 Brugada Syndrome 59 pulmonary hypertension PH 59 neurodermatitis 59 Vitamin B# deficiency 59 HLA molecules 59 mitochondrial dysfunction 59 clinically heterogeneous 59 NOMID 59 rheumatic disease 59 myeloproliferative neoplasms 59 immunoregulation 59 cardiac channelopathies 59 bacterium Streptococcus pneumoniae 59 Systemic lupus 59 Thyroid disorders 59 protein misfolding 59 glial tumors 59 immunodeficiencies 59 bone marrow mesenchymal stem 59 etiologic 59 Nonalcoholic fatty liver 59 tauopathies 59 generalized epilepsy 59 ADPKD 59 epilepsies 59 progressive degenerative neurological 59 VIPR2 59 proliferative disorders 59 genetic underpinnings 59 inherited mutations 59 1 diabetes T1D 59 comorbid disorders 59 M. pneumoniae 59 endophenotypes 59 gastrointestinal dysfunction 59 gene rearrangements 59 pain syndromes 59 heritable diseases 59 Sjögren syndrome 59 AAT deficiency 59 glaucoma macular degeneration 59 biologies 59 herpes viruses 59 epigenetic alterations 59 dystonias 59 genetic loci 59 TLR antagonists 59 anemias 59 causative mutations 59 Raynaud syndrome 59 Chronic lymphocytic leukemia 59 Bardet Biedl Syndrome 59 MYH9 59 Genetic variations 59 JAK2 enzyme 58 autoinflammatory 58 VCFS 58 benign paroxysmal positional vertigo 58 paraneoplastic 58 alexithymia 58 multisystemic 58 maladaptive behaviors 58 herpesviruses 58 arterial calcification 58 Systemic lupus erythematosus SLE 58 mitochondrial toxicity 58 Obsessive compulsive disorder 58 Dental caries 58 viral etiology 58 HGPS 58 dissociative disorders 58 pathophysiologic 58 Keratitis 58 Inflammatory bowel disease 58 Pseudomonas aeruginosa infections 58 rheumatologic 58 cypin 58 Brugada syndrome 58 Asperger syndrome Rett syndrome 58 sporadic Creutzfeldt Jakob 58 Meckel Gruber 58 Celiac sprue 58 genomic alterations 58 familial adenomatous polyposis FAP 58 Bullous 58 microRNA expression 58 aetiological 58 myalgic encephalomyelitis ME 58 genomic variation 58 comorbid anxiety 58 systemic scleroderma 58 debilitating neurodegenerative disorder 58 hamartomas 58 genomic variants 58 Cushing syndrome 58 systemic amyloidosis 58 atherothrombosis 58 myeloproliferative 58 prosopagnosia 58 progressive neurodegenerative disorder 58 myeloproliferative disorders 58 hematologic disorders 58 modifier genes 58 atherothrombotic 58 spongiform encephalopathies 58 Major depressive disorder 58 retinal degenerations 58 diabetic retinopathy DR 58 supratentorial 58 phenotypic expression 58 causative gene 58 infantile hemangioma 58 Genetic predisposition 58 pathophysiological processes 58 dentinal hypersensitivity 58 Compulsive hoarding 58 hay fever allergic rhinitis 58 genetic polymorphisms 58 neuropathologic 58 hereditary deafness 58 Myelodysplastic syndrome 58 neurobiological disorders 58 Raynaud disease 58 Alzheimer pathology 58 biochemical mechanisms 58 Epstein Barr Virus EBV 58 Viral infections 58 rheumatoid arthritis multiple sclerosis 58 epilepsy Parkinson disease 58 Essential tremor 58 PIK3CA 58 obstructive sleep 58 deacetylase inhibitors 58 neuro inflammatory 58 tRNA synthetases 58 WDR# 58 Epileptic seizures 58 esophageal reflux 58 optica 58 epigenetic markers 58 neurosensory 57 chronicity 57 TACI mutations 57 drug metabolizing enzymes 57 constipation OIC 57 myopathies 57 Huntingtons disease 57 diabetic kidney 57 genes encode proteins 57 pathophysiological 57 ependymomas 57 fungal organisms 57 invasive secretory carcinoma 57 neuropsychological impairments 57 heritable genetic 57 miRNA molecules 57 IL#R 57 susceptibility loci 57 phenotypic differences 57 channelopathies 57 Wernicke Korsakoff syndrome 57 metabolic dysfunction 57 sortilin 57 Hypertrophic cardiomyopathy 57 intracellular signal transduction 57 mastocytosis 57 familial adenomatous polyposis 57 TCF#L# gene 57 parainfluenza virus 57 rheumatic diseases 57 familial clustering 57 Chronic Inflammatory Demyelinating Polyneuropathy 57 CA MRSA infections 57 Nasal allergies 57 nongenetic 57 FASPS 57 causal pathways 57 WAGR syndrome 57 motor neuron degeneration 57 somatic mutations 57 neurologic disorders 57 tic disorders 57 optic neuropathy NAION 57 Lyme arthritis 57 ectodermal dysplasia 57 autism neurological disorder 57 cardiac conduction 57 Karayiorgou 57 affective psychoses 57 gluten sensitive enteropathy 57 vascular cognitive impairment 57 sCJD 57 cell signaling pathways 57 monogenic disorders 57 virulence genes 57 benign neoplasms 57 Vitamin D insufficiency 57 vWD 57 neuro degenerative diseases 57 disorders FASD 57 Overactive bladder 57 degenerative retinal diseases 57 lysosomal storage disease 57 Hashimoto thyroiditis 57 myotonia 57 neoplastic diseases 57 autosomal recessive 57 molecular determinants 57 GIST tumors 57 Barrett esophagus precancerous 57 autoimmune thyroid 57 DISC1 gene 57 IDH mutations 57 rheumatic disorders 57 progressive neurodegenerative 57 autonomic dysfunction 57 Primary immunodeficiency 57 somatic symptoms 57 idiopathic pulmonary 57 Zinc deficiency 57 incurable neurodegenerative disease 57 FGFs 57 podocytes 57 heritable disorders 57 neurological disorder affecting 57 Meckel Gruber syndrome 57 Atopic eczema 57 fronto temporal dementia 57 Spasticity 57 neurodevelopmental disorders 57 amyloid deposition 57 extramedullary 57 postoperative delirium 57 pathological manifestations 57 NOD2 57 enterotypes 57 neuroligins 57 Kufs disease 57 Interstitial cystitis 57 untreated celiac disease 57 herpes zoster shingles 57 serine proteases 57 glomerulonephritis 57 tyrosine kinases 57 Acute respiratory infections 57 Chronic constipation 57 EoE 57 Parkinson disease neurodegenerative disorder 57 pharmacogenetic tests 57 HLA B# 57 somatization disorder 57 neurocognitive impairment 57 Thyroid nodules 57 Inflammatory arthritis 57 Chronic bronchitis 57 LRP5 57 Ehrlichia 57 G#S [002] 57 #q# deletion 57 heterotaxy 57 ubiquitin ligases 57 Opioid induced bowel dysfunction 57 IgA deficiency 57 C1q 57 non coding RNA 57 Tourette syndrome TS 57 lupus scleroderma 57 medulloblastoma malignant brain tumor 57 Polycystic ovary syndrome PCOS 57 hemoglobinopathies 57 neurologic disorder 57 NPHP 57 hereditary nonpolyposis colorectal cancer 57 neuronal dysfunction 57 immunocompetent 57 primary biliary cirrhosis 57 autism spectrum disorders ASDs 57 genetic locus 57 genetic heterogeneity 57 lysosomal diseases 57 distinct subtypes 56 Alzheimers disease 56 chromosomal translocations 56 Lafora disease 56 differential gene expression 56 neurodevelopmental disorder 56 GPC5 56 progranulin mutations 56 Autism Spectrum Disorders ASDs 56 GBA mutations 56 microvascular disease 56 neurobiological disorder 56 vascular endothelial dysfunction 56 Peutz Jeghers syndrome 56 epigenetic changes 56 rhinovirus infection 56 Chronic inflammation 56 familial ALS 56 apoptotic pathway 56 torsade de pointes 56 deafness blindness 56 Relapsing remitting MS 56 Pulmonary fibrosis 56 inherited retinal 56 underlying vasculopathy 56 cytomegalovirus CMV 56 rheumatoid arthritis lupus 56 underlying molecular mechanisms 56 XMRV infection 56 endocrine diseases 56 Cardiac hypertrophy 56 lateral sclerosis ALS 56 etiologic factors 56 Prosopagnosia 56 frontotemporal dementia 56 pathophysiologic mechanism 56 Allergic rhinitis 56 neuroprotective therapies 56 phenotypic variation 56 APOE genotype 56 dysmotility 56 neuroblastomas 56 neurogenerative diseases 56 stress cardiomyopathy 56 microdeletions 56 molecular biomarkers 56 miRNA expression 56 missense mutations 56 vitamin D receptors 56 Bronchiolitis 56 hyperplastic 56 dementing 56 causal variants 56 SSc 56 neurologic diseases 56 Churg Strauss syndrome 56 signaling cascades 56 neurexins 56 vascular dysfunction 56 methylation patterns 56 EBV infection 56 Candida overgrowth 56 insulin resistance syndrome 56 euthymic patients 56 Retinitis pigmentosa 56 Parkinson disease epilepsy 56 SHANK3 gene 56 cause cardiac channelopathies 56 fatal neurodegenerative disorder 56 polyglutamine diseases 56 Magnesium deficiency 56 Dilated cardiomyopathy 56 macular degeneration diabetic retinopathy 56 liver cancers hypercholesterolemia 56 Glucocorticoids 56 genetic aberrations 56 impaired cognition 56 arthritis RA 56 nephronophthisis 56 CDH1 56 Nephrogenic Systemic Fibrosis NSF 56 tumor suppressor protein 56 genetic determinants 56 vertebral subluxation 56 Severe Primary IGFD 56 Alpha synuclein 56 neuro developmental disorders 56 Periodontal disease 56 glutamate signaling 56 juvenile idiopathic arthritis 56 MLL2 56 differential diagnoses 56 thrombophilia 56 lichen planus 56 γ secretase 56 epigenetic regulation 56 chronic degenerative diseases 56 musculoskeletal diseases 56 sickle cell cystic fibrosis 56 predisposing factors 56 Leber hereditary optic neuropathy 56 cystic kidney 56 Ischaemic heart 56 Dengue hemorrhagic fever DHF 56 Li Fraumeni syndrome 56 splice junctions 56 Coeliac disease 56 LRRK2 mutations 56 molecular signaling pathways 56 LRRK2 gene 56 chromosomal anomalies 56 colorectal carcinogenesis 56 autoantigens 56 multisymptom illness 56 intestinal microbiota 56 Leber Congenital Amaurosis LCA 56 Respiratory syncytial virus RSV 56 Anxiety disorders 56 cellular pathways 56 proliferative diseases 56 gastric carcinoma 56 STAT4 56 airflow limitation 56 pyelonephritis 56 overactivation 56 myeloproliferative diseases 56 carcinoid 56 hydrops 56 primary hyperparathyroidism 56 fatal neuromuscular disorder 56 exocrine glands 56 autosomal dominant polycystic kidney 56 syndromes 56 glaucoma ischemia 56 holoprosencephaly 56 atherosclerotic disease 56 pituitary adenomas 56 myofascial pain syndrome 56 BMPR2 56 mitochondrial mutations 56 fatal neurodegenerative 56 Beta thalassemia 56 secretory diarrhea 56 polymyalgia rheumatica 56 NF1 56 transmissible spongiform encephalopathies 56 PKU genetic 56 Transverse myelitis 56 Brd4 56 opportunistic pathogens 56 cardiometabolic disorders 56 interleukins 56 Gliomas 56 hereditary disorders 56 Myofascial pain 56 HNPCC 56 ORMDL3 56 biopsychosocial 56 nonalcoholic steatohepatitis 56 innate immune responses 56 prodrome 56 giant cell arteritis 56 γδ T cells 56 Parkinson disease multiple sclerosis 56 Excessive daytime sleepiness 56 Korsakoff syndrome 56 Generalized anxiety disorder 56 astrocytomas 56 aetiology 56 Pulmonary arterial hypertension 56 hormones neurotransmitters 56 immunodeficiency disorder 56 multigenic 55 OSAHS 55 cellular prion protein 55 ASDs 55 hematopoietic malignancies 55 APOL1 55 seizure disorders 55 C. trachomatis 55 diabetes mellitus DM 55 hyperammonemia 55 Obstructive sleep apnea 55 CaM kinase II 55 susceptibility genes 55 autoimmune encephalitis 55 neuroinflammatory 55 engineered RAP peptides 55 pilocytic astrocytomas 55 disabling neurological 55 Bardet Biedl syndrome 55 enteroviruses 55 airway remodeling 55 Nutrient deficiencies 55 flaviviruses 55 hyperinsulinism 55 commensal bacteria 55 microbiomes 55 spinocerebellar ataxia 55 atherothrombotic disease 55 demyelinating disorders 55 sensory receptors 55 increased intestinal permeability 55 hypertrophic cardiomyopathy HCM 55 neuropsychiatric symptoms 55 rheumatoid arthritis inflammatory bowel 55 Joubert syndrome 55 etiological 55 Genetic mutations 55 clonally 55 chronic venous insufficiency 55 macular degeneration glaucoma 55 autosomal dominant disorder 55 hippocampal function 55 RNAi therapeutic targeting 55 cAMP signaling 55 electrophysiologic 55 Allergic diseases 55 Parkinson disease Alzheimer disease 55 tonic clonic seizures 55 atypical hemolytic uremic syndrome 55 atopic disorders 55 thoracic aortic disease 55 chronic autoimmune disorder 55 Brodmann Area 55 mental retardation epilepsy 55 leptin deficiency 55 MGUS 55 erythema nodosum 55 nociceptive pain 55 Acute Bacterial Sinusitis ABS 55 pathophysiological mechanisms 55 renal fibrosis 55 transthyretin amyloidosis 55 rheumatoid arthritis psoriasis 55 opioid antagonists 55 Polycythemia vera 55 cystic fibrosis Duchenne muscular 55 Meningiomas 55 congenital disorders 55 vascular abnormalities 55 behavioral abnormalities 55 beta defensins 55 compensatory mechanisms 55 Autism Asperger Syndrome 55 diarrhea abdominal cramps nausea 55 Vascular dementia 55 Latent TB 55 anosognosia 55 microRNA molecules 55 MAPK pathway 55 Neuropathic pain 55 KRAS oncogene 55 encephalitis meningitis 55 APOE e4 55 presymptomatic 55 muscular dystrophy cystic fibrosis 55 bacteria Streptococcus pneumoniae 55 chlamydial infections 55 eosinophilic esophagitis 55 Polymorphic Ventricular Tachycardia CPVT 55 antibody IgE 55 anatomical abnormalities 55 Rh incompatibility 55 rhinovirus infections 55 chromosome translocations 55 primary ciliary dyskinesia 55 pharmacogenomic tests 55 chromosomal anomaly 55 metaplasia 55 neuroendocrine 55 FTIs 55 Diabetic neuropathy 55 hereditary degenerative 55 N. meningitidis 55 pathogenic mutations 55 carcinoids 55 etiologies 55 folate metabolism 55 neuro vascular 55 chromosomal rearrangements 55 thunderclap headache 55 germline mutations 55 Personality disorders 55 MECP2 gene 55 receptor subtypes 55 leaky gut 55 Male pattern baldness 55 hypothalamic pituitary adrenal axis 55 BCL#A 55 Alleles 55 recessive inheritance 55 AAT Deficiency 55 chromosome #p#.# 55 behavioral disinhibition 55 thyroid hormone deficiency 55 muscular skeletal disorders 55 TMJ disorder 55 Pathological gambling 55 Atypical antipsychotics 55 metastatic neuroendocrine tumors 55 Haptoglobin 55 Cytomegalovirus CMV 55 autoimmune thyroiditis 55 Enbrel Humira 55 emphysema chronic bronchitis 55 Leber congenital amaurosis LCA 55 genetic susceptibilities 55 CYP#C# gene 55 Kabuki syndrome 55 chronic inflammations 55 genomic deletions 55 dyskeratosis congenita 55 Huntington chorea 55 neurofibromatosis type 55 pathogenetic mechanisms 55 structural abnormalities 55 clade B 55 Adenoviruses 55 bullous pemphigoid 55 salivary proteins 55 protein isoforms 55 CALHM1 55 staphylococcal infections 55 Multiple sclerosis MS 55 dysfunctional mirror neuron 55 lactose malabsorption 55 Hereditary angioedema HAE 55 demyelinating disease 55 Hypertensive heart 55 Endometrial cancer 55 myalgic encephalomyelitis 55 testicular dysgenesis syndrome 55 Genetic mutation 55 chromosome #q#.# [001] 55 rotaviruses 55 circadian genes 55 perilipin 55 Pervasive Developmental Disorders 55 tardive dyskinesia TD 55 Iron deficiency anemia 55 Myeloproliferative 55 synaptogenesis 55 Six3 55 pheochromocytoma 55 Lewy body 55 classic autism Asperger 55 genetic alterations 55 CP CPPS 55 neural substrates 55 phenotypic variability 55 sphingolipid 55 Hp2 2 55 epigenetic modifications 55 focal segmental glomerulosclerosis FSGS 55 Parkinson Disease PD 55 physiologic mechanisms 55 embryonal rhabdomyosarcoma 55 GRNOPC1 contains 55 bullous 55 eosinophilic 55 rhinosinusitis 55 breast endometrial 55 somatoform disorders 55 Maroteaux Lamy syndrome 55 cardiomyopathies 55 hypercholesterolemia liver 55 Becker muscular dystrophy 55 fibrotic disease 55 asplenia 55 collagen vascular 55 chromosomal regions 55 recessive genetic 55 PGRN 55 Peritoneal mesothelioma 55 apoE 55 variable immunodeficiency 55 dysregulation 55 inherit predisposition 55 LQTS 55 Valvular heart 55 manic depressive disorder 55 gene APOE4 55 degenerative disorders 55 rhythm disturbances 55 potent inhibitors 55 Pervasive Developmental Disorder 55 haemolytic anemia 55 Ischemic heart 55 Ankylosing spondylitis 55 PCOD 55 disorders 54 S. aureus infection 54 micro RNA 54 ophthalmologic disorders 54 Gorlin syndrome 54 HDACs 54 multiple etiologies 54 eczema asthma 54 chromosome rearrangements 54 Peripheral artery disease 54 inflammatory bowel 54 psychobiological 54 molecular underpinnings 54 mycosis 54 autosomal dominant 54 hematological abnormalities 54 amyloid formation 54 polycystic ovarian syndrome PCOS 54 malignant lymphomas 54 KCNH2 54 urolithiasis 54 latent TB infections 54 Lupus nephritis 54 Plaque psoriasis 54 neurodegenerative disease 54 Bcr Abl mutations 54 myosins 54 chromatin structure 54 Childhood Disorder 54 ichthyosis vulgaris 54 carbohydrate antigens 54 hematologic diseases 54 autoimmune inflammatory 54 Chronic pancreatitis 54 Allergic conjunctivitis 54 hyper IgE syndrome 54 GPCR targets 54 thyroid deficiency 54 postpartum mood 54 neurologic symptoms 54 Schizoaffective disorder 54 neurocognitive deficits 54 Rheumatic fever 54 Diabetic nephropathy 54 microcephalin 54 bacterial prostatitis 54 Panton Valentine leukocidin PVL 54 Sezary syndrome 54 cardiovascular endocrine 54 autoimmune uveitis 54 psychiatric comorbidity 54 Mucositis 54 amyloid protein plaques 54 Venous thromboembolism 54 multiple sclerosis psoriasis 54 Mitochondrial diseases 54 Molnar Szakacs 54 hypereosinophilic syndrome 54 polycythemia vera PV 54 Angelman syndrome 54 viral proteins 54 micro RNAs 54 cardio metabolic diseases 54 levodopa induced 54 antiphospholipid syndrome 54 diabetic microvascular complications 54 disorder FASD 54 Borrelia 54 dermatological disorders 54 Trichomonas vaginalis 54 myelomas 54 Opportunistic infections 54 neurological diseases 54 amnestic MCI 54 Zollinger Ellison Syndrome 54 ceroid lipofuscinosis NCL 54 hyperprolactinemia 54 incurable neurological disorder 54 Parkinsons disease 54 developmental abnormalities 54 exocrine 54 Phenylketonuria PKU 54 hypercoagulable 54 Fetal alcohol 54 Neurofibromatosis type 54 nerve degeneration 54 anticholinergic effects 54 histone deacetylases 54 microdeletion 54 histone modification 54 periodontal pathogens 54 Niemann Pick disease 54 chromosomal deletions 54 allergic inflammation 54 Proteus syndrome 54 Chlamydia pneumoniae 54 biochemical abnormalities 54 neurobiological underpinnings 54 noncontagious disease 54 Alzheimer Disease AD 54 cardio metabolic 54 neurofibroma 54 tic severity 54 Mendelian disorders 54 aneuploid cells 54 bacterium Neisseria meningitidis 54 fatal myelination disorder 54 disorder ASD 54 dysgraphia 54 thyroid dysfunction 54 myotonic dystrophy 54 essential thrombocythemia 54 rheumatological 54 dystrophies 54 microRNA biomarkers 54 medulloblastomas 54 diagnostic biomarkers 54 hyperglycaemia 54 chronic inflammatory bowel 54 transfusion syndrome 54 cholinergic tone 54 Takotsubo cardiomyopathy 54 Lactose intolerance 54 Multiple logistic regression 54 ADAMTS# 54 genetic lysosomal storage 54 schizotypal 54 neurological complications 54 Degenerative diseases 54 metabolic syndrome MetS 54 lymph node enlargement 54 inactivating mutations 54 meta cognitive 54 cardioembolic stroke 54 Alport syndrome 54 Fibromyalgia syndrome 54 abnormal clotting 54 chromosome aberrations 54 Lewy bodies DLB 54 neuroanatomical 54 biochemical imbalance 54 Uncontrolled hypertension 54 deCODE Glaucoma TM 54 flavivirus 54 Hurthle cell 54 Malignant tumors 54 protein tau 54 leukoencephalopathy 54 mycosis fungoides 54 severely immunosuppressed 54 picornavirus 54 severe dehydrating diarrhea 54 psychiatric illnesses 54 pediatric cataract 54 K ras mutations 54 prion disease 54 Irritable Bowel Syndrome IBS 54 liver cancers TTR 54 telomere dysfunction 54 achromatopsia 54 pre mRNA splicing 54 previously undescribed 54 Seborrheic dermatitis 54 prognostic markers 54 allograft rejection 54 mediated autoimmune diseases 54 noninfectious 54 TSLP 54 gliosis 54 Hoarseness 54 hypovitaminosis D 54 SCN5A 54 diabetes dyslipidemia 54 neuropathic pain spasticity 54 multigene 54 immunosuppressed patients 54 opioid peptides 54 neuronal nicotinic receptors NNRs 54 Cognitive impairment 54 Basal cell carcinoma 54 demyelinating 54 Hereditary angioedema 54 familial aggregation 54 disordered breathing 54 Fragile X Syndrome 54 Bronchiectasis 54 gene deletions 54 Velculescu 54 Sjogren syndrome 54 INF2 54 cognitive dysfunctions 54 coagulation abnormalities 54 neuro degenerative 54 Hurler syndrome 54 chronic periodontitis 54 psychiatric disorders 54 cirrhosis liver failure 54 schizophrenia bipolar disorders 54 mucosal immunity 54 costimulatory 54 osteoarthritis rheumatoid arthritis 54 coagulation disorders 54 osteosarcomas 54 parasitic flatworms 54 disease NAFLD 54 autosomal recessive genetic 54 uncharacterized genes 54 Lenzenweger 54 pyoderma 54 nondemented 54 lung adenocarcinoma 54 systemic lupus erythematosus 54 leukodystrophies 54 epiglottitis 54 diseases 54 predisposing factor 54 hepatic steatosis 54 Malignant mesothelioma 54 metabolic disturbances 54 trigeminal 54 identify protein biomarkers 54 temporomandibular joint disorder 54 TMEM#B 54 neurologic complications 54 EEG biofeedback 54 gene expression assays 54 histone modifications 54 nonsense mutations