Related by context. All words. (Click for frequent words.) 58 Parkinsons Disease 58 ectodermal dysplasia 58 Dysplasia 58 recessively inherited 57 discoid lupus 57 Myocarditis 57 rare chromosomal disorder 57 Proteus syndrome 56 retinitis pigmentosa degenerative 56 Hemochromatosis 56 Myositis 56 Acute Leukemia 55 Eosinophilic 55 dominantly inherited 55 Spinal muscular atrophy 55 hereditary hemorrhagic telangiectasia 55 imperfecta 55 Angelman 55 Hand Arm Vibration 55 von Hippel Lindau 55 Holoprosencephaly 54 Brugada Syndrome 54 Langerhans cell histiocytosis 54 Essential Tremor 54 medium chain acyl 54 congenital muscular dystrophy 54 Noonan Syndrome 54 Congenital 54 Cockayne syndrome 54 PNET 54 Wiskott Aldrich Syndrome 54 Hip Dysplasia 54 Apert syndrome 54 Alopecia Areata 53 Chiari Malformation 53 Ectodermal Dysplasia 53 paraneoplastic 53 Congenital Adrenal Hyperplasia 53 hereditary spastic paraplegia 53 recessive genetic 53 Syringomyelia 53 Nodule 53 Epstein Barr Virus 53 holoprosencephaly 53 Lewy Body 53 Myasthenia gravis 53 Retinoblastoma 53 Adrenoleukodystrophy 53 Sudden Arrhythmic Death 53 aniridia 53 Medullary 53 Neurofibromatosis type 52 autosomal recessive genetic 52 choriocarcinoma 52 autosomal dominant polycystic kidney 52 Wegener Granulomatosis 52 Dystrophy 52 Sjogren Syndrome 52 gene MECP2 52 Treacher Collins syndrome 52 Osteogenesis imperfecta 52 Hirschsprung Disease 52 Transverse Myelitis 52 polymyalgia rheumatica 52 Hemolytic 52 congenital disorders 52 Myopathy 52 Moebius Syndrome 52 Hashimoto thyroiditis 52 Malformation 52 systemic amyloidosis 52 VCFS 52 Arteriosclerosis 52 Arnold Chiari Malformation 52 multisystem disease 52 Abstract P# [002] 51 dysgenesis 51 Trigeminal Neuralgia 51 Ichthyosis 51 CMML 51 Cognitive dysfunction 51 variable immunodeficiency 51 Tuberous Sclerosis 51 Primary Immunodeficiency 51 Vasculitis 51 chromosome abnormality 51 Arteriovenous Malformation 51 primary ciliary dyskinesia 51 immunodeficiency disorder 51 Henoch purpura 51 Cytomegalovirus 51 Polycystic Ovary Syndrome 51 Necrotizing Fasciitis 51 DiGeorge Syndrome 51 Dwarfism 51 haemochromatosis 51 Klinefelter Syndrome 51 systemic mastocytosis 51 Niemann Pick disease 51 congenital cataract 51 MELAS 51 dysautonomia 51 Polycystic ovary syndrome PCOS 51 spastic diplegia 51 Hip dysplasia 51 juvenile dermatomyositis 50 Chiari malformation 50 Hutchinson Gilford progeria 50 Krabbe Disease 50 bacterial endocarditis 50 hereditary degenerative 50 Neurofibromatosis Type 50 Retinitis Pigmentosa RP 50 osteopetrosis 50 Chronic fatigue 50 sporadic Creutzfeldt Jakob 50 Respiratory Syncytial Virus 50 histiocytosis 50 Fetal Alcohol 50 Shy Drager syndrome 50 ventricular cardiomyopathy 50 aneuploidies 50 Prenatal diagnosis 50 chronic autoimmune disorder 50 Arrhythmogenic Right Ventricular Cardiomyopathy 50 inflammatory demyelinating 50 R#W [002] 50 Hypophosphatasia 50 Severe Combined Immunodeficiency 50 Idiopathic 50 Hypertrophic 50 Sanfilippo Syndrome 50 Klippel Trenaunay Syndrome 50 CFS ME 50 Fibrosis 50 hyperparathyroidism 50 xeroderma pigmentosum 50 paraganglioma 50 Syndrom 50 Acidosis 50 Chemotherapy induced 50 mastocytosis 50 Hirschsprung disease 50 Sandhoff disease 50 lysosomal storage disease 50 Ehlers Danlos syndrome 50 Arrhythmogenic 50 Eosinophilic Esophagitis 49 Sclerosing 49 dissecans 49 enterocolitis 49 Pelizaeus Merzbacher disease 49 Meckel Gruber 49 Hyperthyroidism 49 Patellofemoral 49 Crouzon syndrome 49 mitochondrial myopathy 49 roseola 49 Clubfoot 49 degenerative neuromuscular disease 49 optic atrophy 49 Palsy 49 Myelodysplastic syndrome 49 congenital adrenal hyperplasia CAH 49 Obstructive Sleep Apnoea 49 multiple sclerosis lupus 49 Phenylketonuria 49 Meniere Disease 49 Alport syndrome 49 Myalgic Encephalomyelitis 49 myalgic encephalomyelitis 49 Perthes disease 49 Crouzon Syndrome 49 Pemphigus 49 FCAS 49 familial adenomatous polyposis FAP 49 myelopathy 49 tricuspid atresia 49 hydatid disease 49 cardio myopathy 49 Streptococcus agalactiae 49 Pompe Disease 49 giant cell arteritis 49 fibrodysplasia ossificans progressiva 49 Rheumatoid 49 cerebri 49 autosomal dominant disorder 49 erythema nodosum 49 Granulomatous 49 Testicular 49 Great Imitator 49 blastoma 49 channelopathies 49 SADS 49 Hypospadias 49 neuro degenerative disorder 49 de novo mutations 49 optic nerve hypoplasia 49 monoclonal gammopathy 49 Malformations 49 Crigler Najjar syndrome 49 Acute Renal Failure 49 hypoplastic 49 Lou Gehrigs disease 49 Oppositional Defiant Disorder 49 Kawasaki Disease 49 lichen planus 49 Primary Pulmonary Hypertension 49 Brainstem 49 Osteosarcoma 48 dyskeratosis congenita 48 Dyspraxia 48 Polycystic Ovarian Syndrome 48 Krabbe Leukodystrophy 48 retrovirus XMRV 48 cerebellar hypoplasia 48 Acute Myelogenous Leukemia 48 Immune Deficiency 48 Epidermolysis bullosa 48 Encephalomyelitis 48 Cerebellar 48 septo optic dysplasia 48 Myotonic dystrophy 48 Haemorrhage 48 skeletal malformations 48 Porphyria 48 velo cardio facial 48 ocular albinism 48 myositis 48 congential 48 pyloric stenosis 48 Endocarditis 48 autosomal recessive disease 48 atypical scrapie 48 myalgic encephalomyelitis ME 48 hemorrhagic colitis 48 degenerative neurological disease 48 Irritable Bowel 48 fronto temporal dementia 48 hypoplasia 48 CHD7 48 Chronic Pelvic Pain 48 spastic paraplegia 48 Reflex Sympathetic Dystrophy 48 thyroid dysfunction 48 pulmonary hypertension PH 48 polycystic kidneys 48 congenital glaucoma 48 hypotonia 48 diaphragmatic hernia 48 Diamond Blackfan anemia 48 Dravet syndrome 48 autosomal recessive disorder 48 Von Hippel Lindau 48 eosinophilic 48 Chronic Myelogenous Leukemia 48 Congenital Muscular Dystrophy 48 Vulvodynia 48 Metastases 48 Churg Strauss syndrome 48 pseudotumor cerebri 48 Treacher Collins 48 neoplasias 48 obliterans 48 Tuberous Sclerosis Complex 48 myocarditis inflammation 48 Leber Congenital Amaurosis LCA 48 Spasticity 48 Hypothyroidism 48 neurologic deficits 48 osteodystrophy 48 Li Fraumeni syndrome 47 Von Willebrand disease 47 nephritis 47 infantile hemangioma 47 Morgellons Disease 47 renal allograft 47 Hyperkalemia 47 Spina bifida 47 nephrosis 47 cryptogenic 47 Sydrome 47 Nonspecific 47 Spinal Meningitis 47 polymyalgia 47 Keratoconus 47 congenital disorder 47 Necrotizing fasciitis 47 Lameness 47 Articular 47 autoimmune thyroiditis 47 embryonal rhabdomyosarcoma 47 motor neurone 47 Prolapse 47 germline mutations 47 epidermolysis bullosa 47 Acute Lymphoblastic Leukaemia 47 GBA mutations 47 Guillain Barr 47 hypogonadotropic hypogonadism 47 Syndrome SADS 47 urolithiasis 47 Usher Syndrome 47 pernicious anemia 47 MD CCFP 47 Hallux 47 inherited retinal 47 degenerative disorder 47 interstitial nephritis 47 genetic syndromes 47 Keratitis 47 Multivariate analysis 47 Angelman syndrome 47 hydrops 47 macular disease 47 fructose intolerance 47 heart syndrome HLHS 47 cerebellar ataxia 47 Trigeminal neuralgia 47 Sjögren syndrome 47 Hypoplastic Left Heart 47 Leber congenital amaurosis 47 Reflex Sympathetic Dystrophy Syndrome 47 hereditary hemochromatosis 47 leaky gut 47 Synovial Sarcoma 47 medial tibial stress 47 1 Antitrypsin Deficiency 47 acute myocarditis 47 ataxia telangiectasia 47 pigmentosa 47 sacral agenesis 47 Thrombotic 47 Urticaria 47 Encephalopathy 47 Leukodystrophy 47 Adrenal 47 DiGeorge syndrome 47 Osteogenesis Imperfecta 47 Hydrocephalus 47 Hemorrhagic 47 Chronic Fatigue Syndrome CFS 47 Wilms Tumor 47 Periodontitis 47 Morquio syndrome 46 Congenital Heart Disease 46 Motor neurone disease 46 Hereditary angioedema 46 agenesis 46 androgenetic alopecia 46 hemolytic anemia 46 tuberous sclerosis complex 46 CHARGE syndrome 46 Neurofibromatosis 46 Polio Syndrome 46 somatization disorder 46 hereditary deafness 46 incurable neurodegenerative disease 46 Ebstein anomaly 46 aciduria 46 degenerative neurological disorder 46 Sudden Arrhythmia Death 46 Disease GVHD 46 disorder thalassemia 46 leptin deficiency 46 Neimann Pick 46 Interstitial cystitis 46 arthrogryposis 46 radiculopathy 46 Pancreatic 46 hypertrophic cardiomyopathy HCM 46 Amblyopia 46 Medulloblastoma 46 diffuse intrinsic pontine glioma 46 congenital anomaly 46 Ectopia Cordis 46 Ultrasonography 46 Beta thalassemia 46 cystic fibrosis chronic pancreatitis 46 encephalomyelitis 46 Shwachman Diamond Syndrome 46 valvular heart disease 46 transcranial Doppler ultrasound 46 Anaemia 46 Sclerosis 46 Melasma 46 intestinal polyps 46 Genetic mutation 46 Guillain Barré Syndrome 46 Wolf Hirschhorn 46 Rh factor 46 progressive neurodegenerative disorder 46 metachromatic leukodystrophy 46 Nat Genet 46 #:#-# [037] 46 Atrophy 46 renal fibrosis 46 idiopathic epilepsy 46 syringomyelia 46 multisystem disorder 46 haemolytic anemia 46 degenerative neurological condition 46 leukoencephalopathy 46 brain malformation 46 aphthous stomatitis 46 Oedema 46 disorders FASD 46 Tachycardia 46 Anencephaly 46 hereditary blindness 46 neuritis 46 Marfan Syndrome 46 Graves ophthalmopathy 46 chromosomal disorder 46 spasmodic torticollis 46 malignant hyperthermia 46 Canavan Disease 46 hypercoagulability 46 Joubert syndrome 46 Social Anxiety Disorder 46 CLINICAL PHARMACOLOGY 46 chromosomal defect 46 neurologic disorder 46 Alzheimer Dementia 46 Chronic Sinusitis 46 Abnormality 46 spongiform encephalopathies 46 Polymorphic Ventricular Tachycardia CPVT 46 eosinophilic inflammation 46 Bronchiectasis 46 Battens Disease 46 mosaicism 46 cardiac channelopathies 46 Lymphoproliferative 46 Olanow 46 NQO1 46 Bronchiolitis 45 myeloproliferative neoplasms MPNs 45 autoimmune thyroid 45 proband 45 Foetal alcohol 45 thrombophilia 45 Infantile 45 Gallstone 45 neonatal lupus 45 Enuresis 45 autosomal recessive 45 benign positional vertigo 45 Gynecomastia 45 Nephrotic Syndrome 45 Deep Vein Thrombosis 45 Brugada syndrome 45 Nephropathy 45 Klinefelter syndrome 45 Ataxia 45 metaplasia 45 Apert 45 polycystic ovary 45 osteogenesis imperfecta OI 45 Urinary tract infection 45 Lafora disease 45 alveolar rhabdomyosarcoma 45 Sleep Apnoea 45 CIAS1 45 Macular Dystrophy 45 skeletal dysplasia 45 polycystic ovary syndrome 45 Usher syndrome 45 familial polyposis 45 Cellulitis 45 Neuropathic 45 recessive inheritance 45 Immune Thrombocytopenic Purpura 45 Fibromyalgia Chronic Fatigue Syndrome 45 Nonalcoholic fatty liver 45 Alkaline Phosphatase 45 recessive trait 45 IgA deficiency 45 Bruxism 45 hereditary nonpolyposis colorectal cancer 45 Mitochondrial Dysfunction 45 coxsackievirus 45 spastic cerebral palsy 45 HNPCC 45 primitive neuroectodermal tumor 45 monogenic 45 Chemical Sensitivity 45 chiari malformation 45 cystic fibrosis Duchenne muscular 45 myeloproliferative 45 Helps Diagnose 45 cardiac fibrosis 45 Muscular dystrophy 45 ME CFS 45 Stargardt Macular Dystrophy 45 allelic variants 45 Hurler syndrome 45 Rhabdomyolysis 45 dysplasia 45 chronic obstructive airway 45 Benign Paroxysmal Positional Vertigo 45 Alopecia 45 Gunderson JG 45 AAT deficiency 45 Genetic susceptibility 45 orthostatic intolerance 45 Pervasive Developmental Disorders 45 Irritable bowel syndrome 45 syndrom 45 paragangliomas 45 pancreatectomy 45 Chronic Lyme disease 45 epididymitis 45 Juvenile Rheumatoid Arthritis 45 Raynaud disease 45 Male Pattern Baldness 45 hypertrichosis 45 #p#.# [001] 45 systemic autoimmune 45 cause cardiac channelopathies 45 Autosomal dominant 45 temporal arteritis 45 Prognostic Factors 45 Hydrocephalus Foundation 45 Hemangioma 45 chronic renal insufficiency 45 Irritable Bowel Syndrome IBS 45 Iatrogenic 45 ADPKD 45 neuroblastoma tumor 45 thyroiditis 44 ataxias 44 rare autosomal recessive 44 Vitamin B# deficiency 44 Bells Palsy 44 congenital deficiency 44 hereditary disorders 44 Fragile X Syndrome 44 Hypoparathyroidism 44 Deformity 44 Rheumatic Fever 44 myofascial pain syndrome 44 Obsessive compulsive disorder 44 promyelocytic leukemia 44 muscle degeneration 44 T1D 44 neurodevelopment disorder 44 Hyperplasia 44 Apnoea 44 auditory neuropathy 44 Kidney Injury 44 diabetes insipidus 44 Aortic stenosis 44 neurological manifestations 44 Dravet Syndrome 44 polydactyly 44 Bardet Biedl syndrome 44 neuro degenerative 44 Chronic Myeloid Leukaemia 44 G6PD deficiency 44 limb girdle muscular dystrophy 44 Sciatica 44 paroxysmal nocturnal hemoglobinuria 44 interstitial cystitis IC 44 incurable degenerative 44 haemolytic uraemic syndrome 44 CFIDS 44 Reflex sympathetic dystrophy 44 Hemophilia B 44 Sudden Unexpected Death 44 Maroteaux Lamy syndrome 44 neurological disorder affecting 44 multigenic 44 aetiological 44 uro genital 44 Chronic Rhinosinusitis 44 neural crest 44 Gastritis 44 myotonic dystrophy 44 Osteopenia 44 neurofibromatosis 44 Testicular Cancer 44 Bovi Shield GOLD 44 testicular tumors 44 Hemolytic Uremic Syndrome 44 Diverticulitis 44 fibrotic lung 44 autosomal dominant inheritance 44 congenital 44 alpha thalassemia 44 microdeletions 44 TCF#L# gene 44 ploidy 44 inherited neurological disorder 44 MECP2 gene 44 NF2 44 cardiac arrythmia 44 spinal muscular atrophy SMA 44 alzheimer disease 44 acute rheumatic fever 44 Vulvar 44 Pulmonary hypertension 44 Cushing syndrome 44 spasmodic dysphonia 44 Retinitis pigmentosa 44 neonatal respiratory distress 44 genetic abnormality 44 Reactive Attachment Disorder 44 Severe Primary IGFD 44 dystrophy 44 myeloproliferative neoplasms 44 Fatty liver 44 Arthrogryposis 44 Genes Discovered 44 idiopathic cardiomyopathy 44 Adrenal Fatigue 44 neurologic symptoms 44 Lou Gherig disease 44 Tick Borne Disease 44 pathophysiologic 44 Autoimmune 44 MYH9 gene 44 pectus 44 Osgood Schlatter 44 Sarcopenia 44 Essential tremor 44 Pernicious anemia 44 Variant Creutzfeldt Jakob Disease 44 prosopagnosia 44 Pulmonary arterial hypertension 44 Weinstock Guttman 44 achromatopsia 44 neuropsychiatric disorder 44 #q#.# [001] 44 pattern baldness 44 WAGR syndrome 44 Rubinstein Taybi syndrome 44 Regurgitation 44 nonhereditary 44 Autistic Spectrum Disorder 44 recessive dystrophic epidermolysis bullosa 44 Postnatal Depression 44 Joubert Syndrome 44 hemochromatosis 43 B Strep 43 progressive neurodegenerative 43 Gall Bladder 43 lactose malabsorption 43 pathognomonic 43 bronchogenic carcinoma 43 ventricular dysplasia 43 Alzheimers Disease 43 intracranial hypertension 43 genetically inherited 43 Dengue Shock 43 Paget Disease 43 autoinflammatory 43 Hypertrophic Cardiomyopathy HCM 43 Cowden syndrome 43 mitochondrial disorders 43 Dystonia 43 Alzeimer 43 Keratosis 43 Polycystic kidney disease 43 HELLP syndrome 43 leukodystrophies 43 FELV 43 Lymphoma Leukemia 43 Feline Leukemia Virus 43 Morquio 43 polydactylism 43 Morton Neuroma 43 Posttraumatic 43 spondylolysis 43 anaerobic bacterium 43 retinal dysfunction 43 incurable genetic 43 autonomic dysfunction 43 kidney insufficiency 43 MGUS 43 schizoaffective disorder bipolar 43 Creutzfeldt Jacob 43 multiple endocrine neoplasia 43 Goldenhar syndrome 43 Long QT syndrome 43 MD FRCS 43 Parkinsons disease 43 Chronic Lyme Disease 43 BCNS 43 chronic venous insufficiency 43 Echocardiographic 43 Hallux valgus 43 inherited genetic mutation 43 ADA SCID 43 autoinflammatory diseases 43 J Foot Ankle 43 genes predisposing 43 dopamine transporter gene 43 Trichotillomania 43 Heredity 43 MRCVS 43 Merkel Cell Carcinoma 43 vascular cognitive impairment 43 Gastroparesis 43 C. Diff 43 neoplastic 43 ECLS 43 incurable neurological disorder 43 Dysautonomia 43 Bovine spongiform encephalopathy BSE 43 Leber congenital amaurosis LCA 43 Coeliac disease 43 Spectrum Disorder 43 autosomal dominant 43 myoclonic epilepsy 43 achondroplasia 43 facioscapulohumeral muscular dystrophy 43 Susceptibility Testing 43 Immunodeficiency 43 #q#.# deletion syndrome 43 Pervasive Developmental Disorder 43 hyperpyrexia 43 Familial 43 immuno deficiency 43 SGPGI Lucknow 43 familial aggregation 43 genetic disorder 43 dystrophies 43 neurodegenerative disorder 43 Ovary 43 Vaccine Shows Promise 43 canine heartworm 43 mitochondrial mutations 43 Rare Genetic 43 spongiform encephalopathy 43 Stress Urinary Incontinence 43 somatic mutation 43 Male pattern baldness 43 congenital cataracts 43 Rhinitis 43 Myotonic Dystrophy 43 Adult Respiratory Distress 43 Krabbe leukodystrophy 43 Pinkeye 43 genetic defect 43 distemper virus 43 hormonal disorder 43 TMJ disorder 43 gene locus 43 chronic urticaria 43 susceptibility alleles 43 postural orthostatic tachycardia 43 shaking palsy 43 Catheter Associated 43 #q# deletion syndrome 43 Preeclampsia 43 undescended testicle 43 bicuspid aortic valve 43 Mastitis 43 torticollis 43 Bedsores 43 Aplastic Anemia 43 extrapyramidal 43 Morquio Syndrome 43 Maroteaux Lamy Syndrome 43 Vertebral 43 Necrosis 43 ichthyosis 43 spontaneous mutation 43 Restless Leg Syndrome 43 Respiratory Distress 43 Scrapie 43 Sudden Adult 43 pheochromocytomas 42 juvenile myelomonocytic leukemia 42 hallux limitus 42 retinitis 42 Peutz Jeghers syndrome 42 lymphocytic choriomeningitis virus 42 paresis 42 Peripheral neuropathy 42 lateral sclerosis ALS 42 Hurthle cell 42 celiac sprue 42 Multiple Chemical Sensitivity 42 malformation 42 congenital abnormalities 42 Sarcoidosis 42 Sexsomnia 42 HLA DRB1 42 Prenatal Diagnostic 42 Syndrome 42 Alopecia areata 42 obstructive coronary artery 42 dilated cardiomyopathy 42 Bedwetting 42 Patau syndrome 42 chronic rheumatic 42 Parkinsonism 42 congenital deformity 42 Tourette Syndrome TS 42 spontaneous remission 42 SIDS Sudden Infant Death 42 subclinical 42 Hutchinson Gilford Progeria Syndrome 42 FXTAS 42 pheochromocytoma 42 Geriatr 42 malformations 42 Lateral Sclerosis 42 progressive neurodegenerative disease 42 McCune Albright 42 progressive neuromuscular 42 Hypersensitivity 42 Respir 42 nonprogressive 42 Oxidative stress 42 Hutchinson Gilford Progeria 42 JAK2 mutation 42 Dissociative 42 Celiac 42 inherited neurodegenerative 42 Six3 42 Ischaemic heart 42 toxic epidermal necrolysis TEN 42 Retinopathy 42 Genetic Diversity 42 CSPG 42 neurodegenerative disorder characterized 42 chromosomal anomalies 42 Diabetic neuropathy 42 syndromic 42 Parkinson degenerative 42 pilocytic astrocytomas 42 lysosomal storage diseases 42 Chagas Disease 42 Ulcer 42 Lou Gherig Disease 42 laryngeal paralysis 42 Familial Dysautonomia 42 LHON 42 contagious equine metritis 42 TP# mutation 42 LRRK2 mutations 42 Excessive sweating 42 Proteus Syndrome 42 Fibro 42 Genotypic 42 ALT elevation 42 progressive retinal degenerative 42 chromosomal anomaly 42 situs inversus 42 keratoconjunctivitis 42 Lupus Erythematosus 42 underactive thyroid gland 42 monozygotic twins 42 moyamoya 42 neurodermatitis 42 adrenal hyperplasia 42 Graft Versus Host 42 Exercise Induced 42 debilitating neurological disorder 42 apolipoprotein E gene 42 monogenic disorders 42 multi infarct dementia 42 filaggrin 42 Atopic dermatitis 42 progressive neurodegenerative disorders 42 spinocerebellar ataxia 42 feline leukemia virus 42 sCJD 42 Mitochondrial dysfunction 42 inheritable genetic 42 Hurler Syndrome 42 Embryo Transfer 42 Obsessive compulsive 42 Alzeheimer 42 ABO blood 42 autonomic neuropathy 42 rheumatic disease 42 Coeliac 42 panleukopenia 42 PALB2 42 exfoliative glaucoma 42 progressive neurological disorder 42 progressive degenerative neurological 42 Endometrial cancer 42 Cyst 42 Pulmonary Artery 41 hereditary predisposition 41 Kleine Levin 41 primary sclerosing cholangitis 41 Compulsive hoarding 41 bacterium Streptococcus 41 BSE Bovine Spongiform 41 Misdiagnosed 41 renal scarring 41 Amyotrophic lateral sclerosis ALS 41 Esophagitis 41 Arch Facial Plast 41 Urinary Tract Infection 41 NADIS 41 bloodborne 41 Hepato 41 inappropriate antidiuretic hormone SIADH 41 Mouse Model 41 fatal neurodegenerative disorder 41 benign paroxysmal positional vertigo 41 Tennis Elbow 41 Short Stature 41 epidermolysis bullosa EB 41 transverse myelitis 41 AAT Deficiency 41 Sickle Cell Anemia 41 static encephalopathy 41 degenerative neurological 41 depersonalization disorder 41 cancerous polyps 41 autoregulation 41 Asberger Syndrome 41 Overactive 41 ARVC 41 NMO 41 bicuspid valve 41 Acute Liver Failure 41 hyperinsulinism 41 Fibromyalgia syndrome 41 Chronic Inflammatory Demyelinating Polyneuropathy 41 nephron 41 oral thrush 41 sporadic ALS 41 polygenic 41 immunodeficiency diseases 41 idiopathic myelofibrosis 41 IMHA 41 autoimmune pancreatitis 41 CDH1 41 eg erythema multiforme 41 Marfan syndrome genetic 41 optic neuropathy 41 retinitis pigmentosa RP 41 hyperhydrosis 41 pyelonephritis 41 TEVAR 41 premature ovarian 41 blood clotting disorder 41 inherited neurodegenerative disorder 41 NF1 41 Inflammatory bowel disease 41 Chronic Insomnia 41 heritable 41 conjunctival hyperemia 41 Binge Eating Disorder 41 Cardiological 41 gallstone disease 41 immune reconstitution inflammatory 41 hereditary 41 Disease 41 Aicardi syndrome 41 predisposing factor 41 Candida overgrowth 41 progranulin gene 41 systemic scleroderma 41 lactase deficiency 41 G#S mutation 41 phenotypic expression 41 idiopathic 41 corneal dystrophy 41 nongenetic 41 Pediatric Neurologist 41 missense mutations 41 Apraxia 41 Colon Polyps 41 alopecia 41 Imaging Diagnostic 41 Translational Oncology 41 microdeletion 41 Analyte 41 Breast Cancers 41 maternally inherited 41 cardiac insufficiency 41 nondemented 41 Hypertrophic cardiomyopathy 41 hyperprolactinemia 41 Scleroderma 41 Obsessive Compulsive 41 anosognosia 41 acute myocardial 41 non polyposis colorectal 41 causative genes 41 Taenia 41 susceptibility gene 41 toxoplasmosis 41 Dilated cardiomyopathy 41 PGAD 41 Conduct Disorder 41 vulvodynia 41 Sudden Unexplained Death 41 proximal femoral