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(Click for frequent words.) 66 etiologies 63 pain syndromes 63 dissociative disorders 62 disorders 61 syndrome 61 etiology 61 aetiology 60 phenotypes 60 psychiatric disorders 60 neurodevelopmental disorders 59 somatic complaints 59 pathologies 59 neurodevelopmental disorder 59 chromosomal anomaly 59 genetic syndromes 59 phenotype 59 Cushing syndrome 59 epilepsies 58 distress syndrome 58 microdeletion 58 neurologic symptoms 58 somatoform disorders 58 neuropsychiatric disorder 58 ataxias 58 neurologic diseases 58 underlying pathophysiology 58 hypochondriasis 58 disorders FASD 58 demyelinating diseases 58 etiologic factors 58 Pervasive Developmental Disorder 58 mitochondrial disorders 57 thyroiditis 57 myopathies 57 alexithymia 57 susceptibility genes 57 myeloproliferative neoplasms 57 paraneoplastic 57 chromosomal deletions 57 idiopathic 57 Not Otherwise Specified 57 pathophysiologic 57 subsyndromal 57 Inflammatory bowel disease 57 autosomal dominant disorder 57 PTEN mutations 56 predisposing factors 56 mitochondrial dysfunction 56 muscular dystrophies 56 motor neuron diseases 56 de novo mutations 56 neurasthenia 56 autoinflammatory diseases 56 abnormalities 56 myalgic encephalomyelitis ME 56 Autistic Disorder 56 Hashimoto thyroiditis 56 neoplastic 56 untreated celiac disease 56 neurologic disorders 56 rheumatic disease 56 monoclonal gammopathy 56 Shy Drager syndrome 56 congenital anomalies 56 Idiopathic 56 myositis 56 ciliopathies 56 prodrome 56 autoinflammatory 56 inherited neurological disorder 56 Churg Strauss syndrome 56 autoimmune thyroiditis 56 neuropathies 56 behavioral abnormalities 56 Anxiety disorders 56 neurological manifestations 55 Inflammatory bowel diseases 55 Cognitive impairment 55 familial adenomatous polyposis 55 paragangliomas 55 neuropsychiatric disorders 55 pathogenic mechanisms 55 chronicity 55 Obsessive compulsive disorder 55 dominantly inherited 55 PANDAS 55 autosomal dominant 55 IgA deficiency 55 missense mutations 55 hormonal abnormalities 55 neuropsychiatric diseases 55 neoplasms 55 immunodeficiencies 55 subtypes 55 Reflex sympathetic dystrophy 55 pathophysiology 55 monogenic 55 lysosomal storage diseases 55 anemias 55 Frontotemporal dementia 55 epididymitis 55 hereditary predisposition 55 hyperplastic 55 psychiatric illnesses 55 mental retardation epilepsy 55 systemic autoimmune 55 Venous thromboembolism 55 syndromal 55 Brugada Syndrome 55 Cluster headaches 55 anosognosia 55 neoplasm 55 Sjögren syndrome 55 giant cell arteritis 55 incurable neurodegenerative disease 55 degenerative disorders 54 neurodegenerative disorder 54 rare autosomal recessive 54 parkinsonism 54 asplenia 54 Posttraumatic stress disorder 54 Childhood Disorder 54 neuronal dysfunction 54 mood disorders 54 neurological abnormalities 54 Irritable bowel syndrome 54 sporadic ALS 54 lymphocytic 54 spastic colon 54 #q#.# [002] 54 cardiomyopathies 54 hamartomas 54 Dysplasia 54 Genetic variants 54 thyroid dysfunction 54 Severe Combined Immunodeficiency 54 pyelonephritis 54 glomerulonephritis 54 malperfusion 54 Compulsive hoarding 54 somatization 54 aneuploidies 54 cystic lesions 54 generalized epilepsy 54 autoimmune disorders 54 anatomical abnormalities 54 coprolalia 54 Chronic fatigue syndrome 54 unknown etiology 54 dysthymic disorder 54 Kraepelin 54 optic atrophy 54 pathological 54 vulvodynia 54 Bardet Biedl syndrome 54 Sydenham chorea 54 thyrotoxicosis 54 systemic lupus erythematosus 54 autoimmune thyroid 54 prodromal 54 involuntary tics 54 nosology 54 somatic symptoms 54 metabolic abnormality 54 puerperal psychosis 54 lysosomal storage disease 54 somatization disorder 54 paresis 54 chromosome abnormality 54 Cowden syndrome 54 osteochondromas 54 FTLD 54 Parkinsonian Syndromes 54 cognitive dysfunction 54 pathophysiological 54 Oppositional Defiant Disorder 53 myalgias 53 Klinefelter syndrome 53 rheumatic diseases 53 VCFS 53 hematologic disorders 53 comorbid disorders 53 degenerative neurological diseases 53 rheumatoid arthritis lupus 53 mood dysregulation 53 Henoch purpura 53 pathophysiological mechanisms 53 Psoriatic arthritis 53 Hemangiomas 53 insulin resistance syndrome 53 congenital disorders 53 symptomatology 53 Myotonic dystrophy 53 Severe Primary IGFD 53 childhood disintegrative disorder 53 Mood disorders 53 myeloproliferative 53 immunocompetent 53 MGUS 53 essential thrombocythemia 53 paraganglioma 53 affective disorders 53 Brodmann Area 53 autosomal recessive disorder 53 Prion diseases 53 mito 53 olfactory dysfunction 53 autosomal recessive 53 subclinical 53 sequelae 53 mosaicism 53 Li Fraumeni syndrome 53 alleles 53 comorbid anxiety 53 motor tics 53 dissociative symptoms 53 metabolic abnormalities 53 tonic clonic seizures 53 dementia praecox 53 somatoform disorder 53 behavioral disinhibition 53 Major depressive disorder 53 primary ciliary dyskinesia 53 pathogenesis 53 Cognitive dysfunction 53 symptoms 53 Leber hereditary optic neuropathy 53 parkinsonian 53 somatic 53 polyarticular 53 osteochondroma 53 myelopathy 53 sonographic appearance 53 leaky gut 53 Neurodegenerative diseases 53 sub syndromal 53 polymyalgia rheumatica 53 rheumatologic 53 osteoarthritis rheumatoid arthritis 53 late infantile neuronal 53 Social Phobia 53 affective psychoses 53 syndromic 53 comorbid depression 53 cretinism 53 Atypical antipsychotics 53 lupus scleroderma 53 myofascial pain syndrome 53 dystrophies 53 genetic aberrations 53 psychotic disorders 53 neurosyphilis 53 FMR1 gene 53 granulomatous 52 ceroid lipofuscinosis NCL 52 Vitamin B# deficiency 52 endophenotypes 52 multisystemic 52 Diabetic neuropathy 52 Korsakoff syndrome 52 posttraumatic 52 aetiological 52 esophageal reflux 52 Chronic Fatigue Syndrome CFS 52 chromosome deletion 52 thrombophilia 52 pulmonary hypertension PH 52 neurological syndromes 52 coagulopathy 52 heritable disorders 52 clefting 52 torticollis 52 Pathological gambling 52 Systemic lupus erythematosus SLE 52 haemolytic anemia 52 akathisia 52 autonomic dysfunction 52 circadian genes 52 compulsive hoarding 52 juvenile idiopathic arthritis JIA 52 Syndrome 52 pyoderma 52 nongenetic 52 cutaneous lesions 52 chromosomal anomalies 52 fungoides 52 viral etiology 52 fatal neuromuscular disorder 52 cryptogenic 52 malformations 52 pathophysiologic mechanisms 52 hyperarousal 52 pituitary tumors 52 dysmotility 52 schizotypal 52 Dilated cardiomyopathy 52 FXTAS 52 MYH9 gene 52 ADPKD 52 genetic polymorphisms 52 Atopic dermatitis 52 #q#.# deletion syndrome 52 juvenile idiopathic arthritis 52 Hyperthyroidism 52 hypersensitivities 52 Comorbid 52 myoclonus 52 leukoencephalopathy 52 Posttraumatic 52 dysgenesis 52 disorder OCD 52 Prenatal diagnosis 52 Hypertrophic 52 post transplant lymphoproliferative 52 connective tissue disorders 52 mycosis fungoides 52 Sleep disordered breathing 52 ANCA associated 52 clinically heterogeneous 52 epigenetic alterations 52 chromosome #p#.# 52 delusional parasitosis 52 neurological diseases 52 polyneuropathy 52 Migraine headaches 52 connective tissue diseases 52 tuberculous 52 dementias 52 Brugada syndrome 52 predisposing factor 52 progressive neurodegenerative disorder 52 fibroma 52 herpesviruses 52 neurologic 52 Myasthenia gravis 52 genetic loci 52 symptomatically 52 hemolytic 52 tic disorders 52 cardiac allograft vasculopathy 52 inflammatory demyelinating 52 variable immunodeficiency 52 arthrosis 52 Ankylosing spondylitis 52 motor neuron degeneration 52 hydrops 52 temporal arteritis 52 hereditary hemochromatosis 52 PDD NOS 52 β thalassemia 52 neurologic disorder 52 karyotypes 52 dyskeratosis congenita 52 fibromatosis 52 polyposis 52 blood clotting disorder 52 neurological disorders 52 Alleles 52 Clinical manifestations 52 osteochondrosis 52 JAK mutations 52 chromosomal defects 52 chromosome #q#.# [001] 52 genetic alterations 52 seminomas 52 Hutchinson Gilford progeria 52 motor neuropathy 52 Raynaud syndrome 52 neurobiological 52 extrapyramidal 52 hamartoma 52 LEOPARD syndrome 52 pathologic 52 idiopathic PAH 52 Zollinger Ellison syndrome 52 ataxia telangiectasia 51 myalgic encephalomyelitis 51 epiglottitis 51 hypoxemia 51 disorders ASD 51 lipomas 51 enteropathy 51 myotonic dystrophy 51 #p#.# [001] 51 deafness blindness 51 recurrent abdominal pain 51 systemic scleroderma 51 incidentalomas 51 Nasal allergies 51 pseudotumor cerebri 51 prostatic hyperplasia 51 CP CPPS 51 NF2 51 chronic autoimmune disorder 51 syndrome FAS 51 autoimmune diseases 51 holoprosencephaly 51 velo cardio facial 51 #q#.# [001] 51 sCJD 51 causative agents 51 dysregulation 51 monozygotic twins 51 motility disorders 51 Pervasive Developmental Disorders 51 toxic megacolon 51 germline mutations 51 inherited mutations 51 neuropathologic 51 lichen planus 51 medically unexplained 51 inherited retinal degeneration 51 monozygotic twin 51 neurobehavioral disorders 51 neurocognitive deficits 51 myelofibrosis polycythemia vera 51 Chronic lymphocytic leukemia 51 dopamine transporter gene 51 Morquio 51 parasomnias 51 EBV infection 51 Acute respiratory distress 51 apolipoprotein E gene 51 AAT Deficiency 51 Binge Eating Disorder 51 encephalitis meningitis 51 Necrotizing fasciitis 51 Osteogenesis imperfecta 51 Hip dysplasia 51 cervicitis 51 hyperreflexia 51 galactosemia 51 intracranial hypertension 51 paralysis blindness 51 radiculopathy 51 arthropathy 51 exotropia 51 LVNC 51 lysosomal diseases 51 hereditary nonpolyposis colorectal cancer 51 hemoglobinopathies 51 celiac sprue 51 recurrent laryngeal nerve 51 ataxia 51 Fetal alcohol 51 superior mesenteric artery 51 situs inversus 51 psychopathologies 51 familial ALS 51 carcinoid tumor 51 diseases 51 recessive inheritance 51 esophagitis 51 emotional lability 51 rhinorrhea 51 Becker muscular dystrophy 51 Bronchiolitis 51 autosomal recessive genetic 51 psychiatric comorbidity 51 Chronic constipation 51 hypogonadotropic hypogonadism 51 CHD7 51 eosinophilic 51 teratoma 51 Excessive daytime sleepiness 51 lumbosacral 51 cervical lymph nodes 51 epithelial tumors 51 EDNOS 51 Allergic rhinitis 51 psychopathology 51 Asperger disorder 51 biopsychosocial 51 multiple etiologies 51 erythema nodosum 51 adrenal hyperplasia 51 arthralgias 51 urethritis 51 dissecans 51 Niemann Pick disease 51 psychiatric diagnoses 51 Magnesium deficiency 51 inflammatory bowel 51 causative gene 51 missense mutation 51 clinicopathologic 51 neuroendocrine 51 APOE ε4 51 Genetic predisposition 51 neonatal respiratory distress 51 gastrointestinal symptoms 51 pathognomonic 51 nonischemic 51 nerve degeneration 51 psychogenic 51 necrotizing 51 genetic lysosomal storage 51 synaptogenesis 51 rheumatoid 51 skeletal abnormalities 51 facioscapulohumeral muscular dystrophy 51 HNPCC 51 MELAS 51 metabolic disorders 51 schwannoma 51 tauopathies 51 Dwarfism 51 autism dyslexia 51 developmental abnormalities 51 nonspecific symptoms 51 skeletal dysplasia 51 Mitochondrial diseases 51 lupus multiple sclerosis 51 hyperexcitability 51 myeloproliferative diseases 51 Chronic fatigue 51 enterocolitis 51 supratentorial 51 dysautonomia 51 acute colitis 51 dystonias 51 genetic determinants 51 Generalized Anxiety Disorder 51 vWD 51 neurobehavioral disorder 51 Graves ophthalmopathy 51 Wernicke Korsakoff syndrome 51 cystic fibrosis chronic pancreatitis 51 primary aldosteronism 51 gene MECP2 51 Mendelian disorders 51 Juvenile Idiopathic Arthritis JIA 51 MECP2 gene 51 euthymic patients 51 afflictions 51 dopamine receptor gene 51 hypermobility 51 AAT deficiency 51 antiphospholipid syndrome 51 Androgenetic alopecia 51 T1DM 51 muscular dystrophy cystic fibrosis 51 Celiac sprue 51 lymph node enlargement 50 rheumatic disorders 50 Congenital 50 familial clustering 50 Leukemias 50 etiologic agent 50 chronic degenerative 50 genetically inherited 50 neurogenerative diseases 50 chromosomal disorders 50 herpes viruses 50 brain lesions 50 glial tumors 50 gestational diabetes mellitus 50 IL#R 50 Irritable bowel syndrome IBS 50 multisystem disorder 50 subtype 50 genetic polymorphism 50 ectodermal dysplasia 50 bullous pemphigoid 50 morphologically 50 SSc 50 myotonia 50 multisystem disease 50 morbidities 50 Chronic sinusitis 50 fatal neurodegenerative disorder 50 frontotemporal dementia 50 hyperinsulinism 50 idiopathic pulmonary 50 neurogenic 50 endocrine disorder 50 cortical dysplasia 50 genomic instability 50 biochemical abnormalities 50 carcinoid 50 syndrome ARDS 50 biochemical imbalances 50 XMRV infection 50 microdeletions 50 blindness paralysis 50 Glucocorticoids 50 Schizoaffective disorder 50 Tay Sachs disease 50 syndrome OSAS 50 chromosome #q# [001] 50 cognitive deficits 50 demyelinating 50 congenital adrenal hyperplasia 50 causal pathways 50 leiomyomas 50 immunodeficiency 50 neuropsychological impairments 50 hereditary spastic paraplegia 50 chromosomal translocations 50 unipolar depression 50 cerebellar hypoplasia 50 tic disorder 50 neurological disorder characterized 50 maladaptive behaviors 50 hormonal disorder 50 derangements 50 Antisocial Personality Disorder 50 hemiparesis 50 polycystic ovarian syndrome PCOS 50 acute myocarditis 50 chronic pelvic 50 oral thrush 50 crohn disease 50 Muscular dystrophy 50 diarrhea predominant IBS 50 congenital anomaly 50 neurofibromatosis type 50 pediatric bipolar disorder 50 dis eases 50 Thyroid disorders 50 nausea vomiting headache 50 Huntingtons disease 50 virulence genes 50 meningitis encephalitis 50 atypical hemolytic uremic syndrome 50 inappropriate antidiuretic hormone SIADH 50 autism Asperger 50 disabling neurological 50 G6PD deficiency 50 TACI mutations 50 benign positional vertigo 50 narcolepsy cataplexy 50 septal defects 50 recessive dystrophic epidermolysis bullosa 50 anterior uveitis 50 mutations 50 autoimmune 50 steatohepatitis 50 neurologic complications 50 atopic 50 #q# deletion 50 HeFH 50 TTR amyloidosis 50 fatal neurodegenerative 50 Lyme arthritis 50 etiologic 50 cognitive dysfunctions 50 #p#.# [002] 50 compulsive disorder 50 idiopathic generalized epilepsy 50 Tourette Syndrome TS 50 hyperhydrosis 50 Binge eating 50 OSAHS 50 ASDs 50 Polymorphic Ventricular Tachycardia CPVT 50 generalized seizures 50 malignancies 50 bone marrow mesenchymal stem 50 Wernicke encephalopathy 50 immunodeficiency disorder 50 calculi 50 hemolytic anemia 50 extrapyramidal symptoms 50 distinct subtypes 50 seborrheic keratoses 50 systemic amyloidosis 50 Fragile X Syndrome 50 eczema asthma 50 convulsive disorders 50 Patellofemoral 50 chronic fatigue syndrome 50 Intussusception 50 bullous 50 mastocytosis 50 recessive trait 50 differential diagnoses 50 disorder ASD 50 nonalcoholic steatohepatitis NASH 50 delusions hallucinations 50 syncope 50 discoid lupus 50 hereditary nonpolyposis colon cancer 50 Bacterial vaginosis 50 physiological abnormalities 50 Arrhythmogenic 50 proliferative disorders 50 haemorrhagic 50 chromosome rearrangements 50 autistic regression 50 myocardial ischemia 50 autistic enterocolitis 50 spongiform encephalopathies 50 SYMPTOMS 50 radiographic findings 50 Aortic stenosis 50 Encephalopathy 50 immune dysregulation 50 orthorexia nervosa 50 lipid abnormalities 50 underdiagnosis 50 Meckel Gruber 50 orchitis 50 Von Willebrand disease 50 chronic renal insufficiency 50 osteosarcomas 50 neuro degenerative disorder 50 lymphoproliferative disorder 50 aneurysmal bone cyst 50 autosomal recessive disease 50 Frontal lobe 50 neurocognitive impairment 50 pharmacological approaches 50 hypokalemia hypomagnesemia 50 stress cardiomyopathy 50 streptococcal 50 Eosinophilic esophagitis 50 Essential tremor 50 genomic rearrangements 50 susceptibility loci 50 homozygous FH 50 neoplasias 50 acetabular dysplasia 50 syndrome gastroesophageal reflux 50 allelic variants 50 urolithiasis 50 Coeliac disease 50 Langerhans cell histiocytosis 50 Chronic pancreatitis 50 multiple sclerosis lupus 50 WAGR syndrome 50 delayed gastric emptying 50 atherothrombotic 50 lactose malabsorption 50 suppurative 50 polyuria 50 chronic degenerative diseases 50 Postpartum psychosis 50 vascular Ehlers Danlos 50 neurogenetic 50 Seasonal affective disorder 50 extramedullary 50 neurofibromas 49 somatic mutations 49 cytopenia 49 denervation 49 Trichophyton rubrum 49 hyperalgesia 49 Spasticity 49 manic depression bipolar disorder 49 neuro degenerative disorders 49 bowel disorders 49 Bardet Biedl Syndrome 49 ADA SCID 49 functional polymorphism 49 intestinal metaplasia 49 psychopathological 49 cellular pathways 49 neuritis 49 recurrent miscarriage 49 myelodysplasia 49 developmental disorders 49 hallucinations psychosis 49 histiocytosis 49 hyper IgE syndrome 49 coexistent 49 subclinical atherosclerosis 49 T1D 49 lupus rheumatoid arthritis 49 exostosis 49 renal fibrosis 49 epigenetic markers 49 atopic disorders 49 polyglutamine 49 erythema migrans 49 A. fumigatus 49 ependymomas 49 chromosomal rearrangement 49 histologic subtypes 49 Tardive Dyskinesia 49 pituitary adenomas 49 primary hyperparathyroidism 49 disorder 49 hippocampal function 49 vaginitis 49 optic neuropathy 49 psychosomatic symptoms 49 Arrhythmogenic Right Ventricular Cardiomyopathy 49 genomic deletions 49 herpes zoster shingles 49 Periodontitis 49 hyperparathyroidism 49 cardiac hypertrophy 49 epilepsy Parkinson disease 49 Body Dysmorphic Disorder 49 Psychiatric Disorders 49 gene polymorphisms 49 gastric distention 49 patella femoral 49 rheumatological 49 endocannabinoid signaling 49 polymorphic ventricular tachycardia 49 #q# deletion syndrome 49 hypoperfusion 49 unprovoked seizures 49 brain malformation 49 mediated autoimmune diseases 49 herpetic 49 subclinical disease 49 fibromyalgia chronic 49 renal diseases 49 Eosinophilic 49 thrombocytosis 49 Rh incompatibility 49 sclerosis ALS 49 dysplastic 49 chromosomal rearrangements 49 Polycythemia vera 49 akinetic 49 dysmorphic features 49 modifier genes 49 bulimia nervosa 49 bipolar disorder schizophrenia 49 neuroinflammation 49 bipolar illness 49 microvascular disease 49 disorder PTSD 49 inflammatory bowel syndrome 49 Malformations 49 GISTs 49 genes predisposing 49 Proteus syndrome 49 schizophrenia bipolar 49 inflammatory bowel disease 49 zoster 49 cardiac abnormalities 49 intestinal disorders 49 artery stenosis 49 hypoplasia 49 myasthenia gravis MG 49 gene variants 49 Leber congenital amaurosis 49 homozygosity 49 frontotemporal 49 Abdominal pain 49 prognostic significance 49 lipid disorders 49 psychosomatic illness 49 hypoplastic 49 IUGR 49 maladies 49 Autoimmune disorders 49 fibrous dysplasia 49 astrocytomas 49 synovial cells 49 nonalcoholic steatohepatitis 49 Bullous 49 fibromyalgia syndrome 49 Ventricular Tachycardia 49 POIS 49 neurobiological disorders 49 fatigue syndrome 49 carcinoid tumors 49 Sanfilippo Syndrome 49 TP# mutation 49 etiological factors 49 cholestasis 49 NOMID 49 fronto temporal dementia 49 arthritis RA 49 autosomal 49 HYPP 49 polymorphisms 49 reflux symptoms 49 Sezary syndrome 49 schizophreniform disorder 49 APOL1 49 congenital 49 pharmacological interventions 49 impingement syndrome 49 allograft rejection 49 leptin deficiency 49 hormonal disorders 49 epilepsy multiple sclerosis 49 acute rheumatic fever 49 phenotypic variability 49 coagulation disorders 49 arthritis osteoporosis 49 nondemented 49 Cancer cachexia 49 Neurofibromatosis type 49 Zollinger Ellison Syndrome 49 dermatitis herpetiformis 49 ABCB1 49 SRBD 49 eating disorders anorexia nervosa 49 constipation predominant irritable bowel 49 neural crest 49 Gastritis 49 LIS1 49 syndrome RLS 49 inflammatory bowel diseases 49 congenital adrenal hyperplasia CAH 49 sleep disorders 49 pneumonias 49 lupus erythematosus 49 septic arthritis 49 intergenic 49 familial adenomatous polyposis FAP 49 respiratory viral infections 49 Cockayne syndrome 49 Chronic Inflammatory Demyelinating Polyneuropathy 49 obstructive sleep 49 piriformis syndrome 49 Iron deficiency anemia 49 progressive dyspnea 49 neurological disorder affecting 49 arrhythmogenic 49 neurodegenerative diseases 49 vascular cognitive impairment 49 hypertrophic 49 vascular dysfunction 49 hypotonia 49 debilitating complication 49 bone deformities 49 penetrance 49 neuroendocrine tumors 49 proliferative diabetic retinopathy 49 SLC#A# [002] 49 mental retardation blindness 49 meniscal tears 49 vitreous hemorrhage 49 hypopituitarism 49 myeloproliferative disorders 49 BDNF gene 49 C1q 49 Nonalcoholic fatty liver 49 psychiatric disorder 49 Chlamydia pneumoniae 49 Primary IGFD 49 genetic underpinnings 49 affective disorder 49 Systemic lupus 49 vestibular schwannomas 49 Hurler syndrome 49 MTHFR 49 Leydig cell 49 functional gastrointestinal disorders 49 Lactose intolerance 49 Mitral regurgitation 49 schizophrenia 49 infarcts 49 vascular anomalies 49 colorectal carcinogenesis 49 marasmus 49 pathophysiologic mechanism 49 susceptibility gene 49 thrombotic thrombocytopenic purpura 49 Hurthle cell 49 anaphylaxis angioedema 49 Haptoglobin 49 arachnoiditis 49 NPHP 49 KCNH2 49 neurobiological disorder 49 hematuria 49 Acid reflux 49 Epidermolysis bullosa 49 genetic variants 49 Myofascial pain 49 Social Anxiety Disorder 49 Dengue Shock 49 lymphoid cells 49 pancytopenia 49 Tay Sachs thalassemia 49 encephalopathy 49 efferent 49 purpura 49 spastic paraplegia 49 Asymptomatic 49 Ehlers Danlos syndrome 49 protein misfolding diseases 49 monogenic diseases 49 disc degeneration 49 subcortical 49 gastric atrophy 49 Epstein Barr 49 primary biliary cirrhosis 49 inflammations 49 receptor subtypes 49 neural disorders 49 vascular endothelial dysfunction 49 anatomic abnormalities 49 PCNSL 49 diabetic kidney 49 symptomology 49 neuroleptic malignant syndrome 49 ectopia 49 Epstein Barr Virus