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(Click for frequent words.) 77 progressive neurodegenerative disorder 74 neurodegenerative disorder 74 inherited neurodegenerative disorder 73 incurable neurological disorder 73 inherited neurodegenerative 73 incurable neurodegenerative disease 72 neuropsychiatric disorder 72 fatal neurodegenerative disorder 72 neurological disorder affecting 72 neuro developmental disorder 71 tics involuntary 71 Essential tremor 71 progressive neurodegenerative 70 monogenic 70 dominantly inherited 70 degenerative disorder 70 progressive neurodegenerative disease 69 autosomal dominant 69 fatal neuromuscular disorder 69 autosomal recessive 69 neurodevelopmental disorder 69 autosomal dominant disorder 69 neurobehavioral disorder 68 neurologic disorder 68 Obsessive compulsive disorder 68 multisystem disease 68 Hutchinson Gilford progeria 68 Myasthenia gravis 67 Pulmonary hypertension 67 degenerative neurological disease 67 Muscular dystrophy 67 autosomal recessive disorder 67 Diabetic neuropathy 67 chronic autoimmune disorder 67 fatal neurodegenerative 67 huntingtin gene 67 Hereditary angioedema HAE 67 chronic neurological disorder 66 neurological disorder characterized 66 Myotonic dystrophy 66 Obstructive sleep apnea 66 degenerative neurological disorder 66 Atopic dermatitis 66 Tourette Syndrome TS 66 inherited retinal degeneration 66 disabling neurological 66 Medulloblastoma 66 degenerative neurological condition 66 Psoriatic arthritis 66 Major depressive disorder 66 complex neurobiological disorder 66 Systemic lupus erythematosus SLE 66 hereditary degenerative 66 autoinflammatory diseases 66 ADPKD 66 ataxia telangiectasia 66 Pulmonary fibrosis 66 Irritable bowel syndrome IBS 66 Cholangiocarcinoma 66 Cockayne syndrome 66 autosomal recessive disease 66 ataxias 66 Leukemias 66 generalized epilepsy 65 neurobiological disorder 65 holoprosencephaly 65 Aortic stenosis 65 Chronic lymphocytic leukemia 65 ceroid lipofuscinosis NCL 65 myalgic encephalomyelitis ME 65 Brugada Syndrome 65 Parkinsonism 65 Retinitis pigmentosa 65 immunodeficiency disorder 65 Acute myeloid leukemia 65 unprovoked seizures 65 Spasmodic dysphonia 65 von Hippel Lindau 65 neurodevelopment disorder 65 progressive degenerative 65 Cystic fibrosis CF 65 Endometrial cancer 65 Chronic sinusitis 65 genetic lysosomal storage 65 inflammatory demyelinating 65 Mitochondrial diseases 65 Tourette syndrome TS 65 Hypophosphatasia 65 Lafora disease 65 Multiple sclerosis MS 65 leukoencephalopathy 65 debilitating neurodegenerative disorder 65 Pompe Disease 65 Leber hereditary optic neuropathy 65 Inflammatory Bowel 65 immunodeficiencies 65 chromosome abnormality 65 Niemann Pick disease 65 dyskeratosis congenita 65 Bulimia nervosa 65 TTR amyloidosis 65 Obstructive sleep apnea OSA 64 Ankylosing spondylitis 64 progressive degenerative neurological 64 Neuropathic pain 64 Systemic lupus 64 spinal muscle atrophy 64 Gastroparesis 64 Chronic pancreatitis 64 Polycystic ovary syndrome PCOS 64 neuro degenerative disorder 64 frontotemporal dementia 64 pseudotumor cerebri 64 paraneoplastic 64 debilitating autoimmune 64 AAT Deficiency 64 epilepsies 64 Becker muscular dystrophy 64 fatal myelination disorder 64 hereditary disorder 64 Epstein Barr Virus 64 AAT deficiency 64 neurodegenerative disorder characterized 64 de novo mutations 64 Aplastic anemia 64 polymorphic ventricular tachycardia 64 multi infarct dementia 64 Irritable bowel syndrome 64 gene MECP2 64 progressive neurodegenerative disorders 64 lysosomal storage diseases 64 recurrent seizures 64 Li Fraumeni syndrome 64 paraganglioma 64 cortical dysplasia 64 lysosomal storage disease 64 Malignant mesothelioma 64 Childhood Disorder 64 Shy Drager syndrome 64 neurodevelopmental disorder characterized 64 Seborrheic dermatitis 64 Brugada syndrome 64 Huntingtons disease 63 neurofibromatosis type 63 Leber congenital amaurosis LCA 63 hereditary spastic paraplegia 63 involuntary tics 63 Frontotemporal Dementia 63 Hyperactivity 63 paragangliomas 63 debilitating neurological disorder 63 Peripheral neuropathy 63 Myopathy 63 Idiopathic pulmonary fibrosis IPF 63 Polycystic kidney disease 63 Sporadic CJD 63 Narcolepsy 63 inherited mutations 63 Retinoblastoma 63 myotonic dystrophy 63 multisystem disorder 63 Hyperthyroidism 63 Pulmonary arterial hypertension 63 Hashimoto thyroiditis 63 myoclonus 63 Inflammatory bowel disease 63 Sanfilippo Syndrome 63 Sjögren syndrome 63 Von Willebrand disease 63 Pervasive Developmental Disorder 63 G#S [002] 63 Magnesium deficiency 63 recessive dystrophic epidermolysis bullosa 63 Coeliac disease 63 sporadic Creutzfeldt Jakob 63 NF2 63 degenerative nerve disorder 63 Iron deficiency anemia 63 Dental caries 63 neuronal dysfunction 63 progressive degeneration 63 Amyotrophic lateral sclerosis 63 dysgenesis 63 Mouse Model 63 variable immunodeficiency 63 Migraine headache 63 mental retardation epilepsy 63 Motor neurone disease 63 Spinal muscular atrophy 63 cramping abdominal pain 63 Interstitial cystitis 63 Hemophilia B 63 neuro degenerative disease 63 ectodermal dysplasia 63 Autoimmune disorders 63 tic disorders 63 Hoarseness 63 Idiopathic Thrombocytopenic Purpura ITP 63 sclerosis ALS 63 FTLD 63 Eosinophilic 63 systemic autoimmune 63 Rhabdomyolysis 63 Pervasive Developmental Disorders 63 phonic tics 63 Vascular dementia 63 Jakob Disease 63 Ulcerative colitis 63 pancytopenia 63 Bardet Biedl syndrome 63 progressive neurological disorder 63 genetic neuromuscular disorder 62 Leber congenital amaurosis 62 Trichotillomania 62 Bronchiectasis 62 fronto temporal dementia 62 spinocerebellar ataxia 62 Parkinsons Disease 62 vascular cognitive impairment 62 torsion dystonia 62 Periodontitis 62 systemic amyloidosis 62 Hereditary angioedema 62 Bronchiolitis 62 WAGR syndrome 62 Angelman syndrome 62 Enlarged prostate 62 Plaque psoriasis 62 autosomal recessive genetic 62 fatal neuromuscular 62 Dravet syndrome 62 hereditary predisposition 62 fibrous dysplasia 62 Herpes simplex virus 62 motor neuron diseases 62 tau pathology 62 Leber Congenital Amaurosis LCA 62 neurological dysfunction 62 chronic inflammatory bowel 62 Basal cell carcinoma 62 Peritoneal mesothelioma 62 bacterium Neisseria meningitidis 62 Bruxism 62 autoinflammatory 62 Vulvodynia 62 ANCA associated 62 Osteogenesis imperfecta 62 Fibrosis 62 dysmotility 62 familial adenomatous polyposis 62 Krabbe Disease 62 Parkinsonian Syndromes 62 Chronic insomnia 62 nerve degeneration 62 familial ALS 62 Lesch Nyhan syndrome 62 Arrhythmogenic Right Ventricular Cardiomyopathy 62 Maroteaux Lamy syndrome 62 motor tics 62 Research www. elsevier.com 62 Rubinstein Taybi syndrome 62 Mucositis 62 muscular dystrophies 62 Epstein Barr virus EBV 62 aneuploidies 62 cystic fibrosis chronic pancreatitis 62 hypothalamic pituitary adrenal axis 62 hormonal disorder 62 Fragile X Syndrome 62 cystic fibrosis Duchenne muscular 62 Parkinson degenerative 62 rare autosomal recessive 62 MELAS 62 neurological manifestations 62 Neurofibromatosis Type 62 Pathological gambling 62 Genetic mutation 62 chorea 62 Tuberous sclerosis 62 Churg Strauss syndrome 61 ataxia telangiectasia AT 61 homocystinuria 61 Eisenmenger syndrome 61 inappropriate antidiuretic hormone SIADH 61 Amyotrophic lateral sclerosis ALS 61 Chorea 61 incurable degenerative brain 61 thyroiditis 61 muscular degeneration 61 Retinitis Pigmentosa RP 61 enterocolitis 61 Ehlers Danlos syndrome 61 Alzheimer Disease AD 61 degenerative neurological diseases 61 #q# deletion 61 Cervical dystonia 61 demyelinating disease 61 inherited degenerative 61 Chronic fatigue 61 Chronic constipation 61 Zinc deficiency 61 leukoencephalopathy PML 61 mastocytosis 61 #q#.# [001] 61 incurable genetic 61 myasthenia gravis MG 61 hereditary deafness 61 Chronic bronchitis 61 Lupus nephritis 61 Tay Sachs thalassemia 61 Essential Tremor 61 Diabetic retinopathy 61 recessive trait 61 Parkinson disease degenerative 61 humans variant Creutzfeldt 61 Epstein Barr Virus EBV 61 Glioma 61 lichen planus 61 frontotemporal dementia FTD 61 muscular dystrophy cystic fibrosis 61 Antisocial personality 61 thyroid hormone deficiency 61 common disabling neurological 61 Korsakoff syndrome 61 complement inhibitor eculizumab 61 Ischemic 61 Hyperkalemia 61 Meningiomas 61 Idiopathic 61 Severe Combined Immunodeficiency 61 Spasticity 61 Critical limb ischemia 61 involuntary movements 61 Parkinson Disease PD 61 overactivation 61 dysphonia 61 Atopic eczema 61 Myelodysplastic syndrome 61 Ribavirin causes 61 oligodendrogliomas 61 Ataxia Telangiectasia 61 spinal muscular atrophy SMA 61 embryonal rhabdomyosarcoma 61 Retinopathy 61 Dwarfism 61 childhood disintegrative disorder 61 recessive inheritance 61 blood clotting disorder 61 chronic granulomatous disease 61 Dilated cardiomyopathy 61 chromosomal anomaly 61 neurological degeneration 61 ataxia 61 Allergic rhinitis 61 channelopathies 61 behavioral abnormalities 61 blastoma 61 Overactive bladder 61 ciliopathies 61 Hypertrophic cardiomyopathy 61 Fatty liver 61 NF1 61 involuntary muscle contractions 61 manic depressive disorder 61 opsoclonus myoclonus syndrome 61 chronic autoimmune 61 myeloproliferative 61 Fanconi Anemia 61 Sleep disordered breathing 61 myelopathy 61 parkinsonism 61 post transplant lymphoproliferative 61 vWD 61 coprolalia 61 idiopathic PAH 61 primary ciliary dyskinesia 61 HGPS 61 missense mutation 61 causative gene 61 herpesviruses 61 Tourette syndrome neurological disorder 61 Genital herpes 61 CNTNAP2 61 Generalized anxiety disorder 61 Trigeminal neuralgia 60 encephalitis swelling 60 Relapsing remitting MS 60 facioscapulohumeral muscular dystrophy 60 autoimmune encephalitis 60 chromosomal defect 60 Chronic renal failure 60 Glioblastoma 60 Neurofibromatosis type 60 Anorexia nervosa 60 Krabbe Leukodystrophy 60 degenerative neuromuscular disease 60 deafness blindness 60 cystic fibrosis muscular dystrophy 60 Apolipoprotein E 60 Peripheral artery disease 60 thrombocytopenia neutropenia 60 autoimmune thyroiditis 60 demyelinating 60 Cryptococcus neoformans 60 leptin deficiency 60 brain malformation 60 glomerulonephritis 60 Idiopathic pulmonary fibrosis 60 JAK2 enzyme 60 myopathies 60 Marfan Syndrome 60 Male pattern baldness 60 anosognosia 60 associated tremor ataxia 60 Hemorrhagic 60 lymphangioleiomyomatosis LAM 60 Penile cancer 60 1 diabetes T1D 60 Joubert syndrome 60 CDH1 60 obesity insulin resistance 60 CHD7 60 lysosomal storage disorder 60 clinically heterogeneous 60 polyglutamine diseases 60 Kleine Levin 60 tuberous sclerosis complex 60 Acute lymphoblastic leukemia 60 Osteosarcoma 60 fungoides 60 Gliomas 60 fibrodysplasia ossificans progressiva FOP 60 Holoprosencephaly 60 Cataplexy 60 Anaplastic 60 Peripheral vascular disease 60 rheumatic disease 60 Premature Aging 60 Adenocarcinoma 60 motor neuron degeneration 60 Papillary 60 airflow limitation 60 syndrome OSAS 60 bacterium Mycobacterium tuberculosis 60 Nonalcoholic fatty liver 60 Bedwetting 60 Oppositional Defiant Disorder 60 incurable neurological 60 Trypanosoma brucei 60 Rhabdomyosarcoma 60 tauopathies 60 Carcinoid tumors 60 optic neuropathy 60 euthymic patients 60 achromatopsia 60 epigenetic alterations 60 Maroteaux Lamy Syndrome 60 apolipoprotein E gene 60 neurodegenerative disease 60 neurological disorder 60 genetic syndromes 60 BRAF gene 60 sensory disturbances 60 renal fibrosis 60 aciduria 60 Atrial fibrillation AF 60 mood dysregulation 60 autosomal dominant polycystic kidney 60 neurofibrillary 60 Proteus syndrome 60 Klippel Trenaunay Syndrome 60 paralysis blindness 60 Henoch purpura 60 myeloproliferative neoplasms 60 transgenic mouse models 60 sickle cell cystic fibrosis 60 nephritis 60 encephalitis meningitis 60 Social Anxiety Disorder 60 molecular abnormalities 60 polymyalgia rheumatica 60 SSc 60 Systemic lupus erythematosus 60 hemolytic anemia 60 Chronic Obstructive Pulmonary 60 Malignant glioma 60 Adrenoleukodystrophy 60 optic atrophy 60 carcinoid tumor 60 generalized dystonia 60 locus coeruleus 60 Myocarditis 60 McCune Albright 60 multiforme 60 genomic variants 60 mycobacterium tuberculosis 60 missense mutations 60 Chronic myeloid leukemia CML 60 Binge eating 60 Friedreich ataxia 60 Schizoaffective Disorder 60 chromosomal disorder 60 Pleural mesothelioma 60 Foodborne botulism 60 systemic scleroderma 60 Genes Identified 60 Bacterial vaginosis 60 CAG repeats 60 spinocerebellar ataxia type 60 Diverticulosis 60 Treatment Shows Promise 60 MC4R gene 60 LHON 60 degenerative retinal disease 60 idiopathic pulmonary 60 Dystrophin 60 Oral mucositis 60 dissociative disorders 60 flaccid paralysis 60 genetically inherited 60 Genetic variants 60 HFE gene 59 chronic progressive neurodegenerative 59 Chronic Inflammatory Demyelinating Polyneuropathy 59 Mental retardation 59 Cluster headaches 59 unknown etiology 59 leiomyomas 59 arthritis RA 59 underlying vasculopathy 59 Urinary tract 59 obliterative bronchiolitis 59 Uncontrolled diabetes 59 tonic clonic seizures 59 MYH9 gene 59 neuroblastoma tumor 59 Juvenile Idiopathic Arthritis JIA 59 dystrophy 59 Diabetic nephropathy 59 Tay Sachs Disease 59 blepharospasm 59 Chronic Pelvic Pain 59 hydrops 59 Emphysema 59 Biliary atresia 59 Rotavirus infection 59 Bullous 59 medium chain acyl 59 MECP2 gene 59 hereditary blindness 59 Arrhythmogenic 59 progressively degenerative 59 Hemorrhagic stroke 59 gastrointestinal dysfunction 59 Glioblastoma multiforme GBM 59 Colorectal cancers 59 Postherpetic neuralgia 59 idiopathic generalized epilepsy 59 Neurodegenerative diseases 59 enzyme deficiency 59 hyperammonemia 59 TSC1 59 Gene Linked 59 leukodystrophy 59 Upregulation 59 CP CPPS 59 Premature ejaculation 59 Cerebral malaria 59 Wiskott Aldrich Syndrome 59 bacterium Streptococcus pneumoniae 59 Kufs disease 59 Hutchinson Gilford Progeria 59 Parkinsons disease 59 BRAF protein 59 disorders FASD 59 Retinal vein occlusion 59 Peutz Jeghers syndrome 59 Hutchinson Gilford Progeria Syndrome 59 neurologic dysfunction 59 Moyamoya disease 59 neuronal degeneration 59 granulomatous 59 infantile hemangioma 59 mitochondrial dysfunction 59 Neurological Disorder 59 Mitral regurgitation 59 pathological hallmark 59 dopamine D4 receptor 59 Hypothyroidism 59 autism neurological disorder 59 Duchenne Muscular Dystrophy DMD 59 immunodeficiency 59 Hurler Syndrome 59 choriocarcinoma 59 Focal dystonia 59 Vitamin B# deficiency 59 demyelination 59 IgA deficiency 59 fibrodysplasia ossificans progressiva 59 Latent TB 59 neurofibroma 59 Angioedema 59 GPC5 59 inherited genetic mutations 59 Acid reflux 59 hematologic disorders 59 manic depression bipolar disorder 59 Tay Sachs genetic 59 Hypertrophic 59 Idiopathic Pulmonary Fibrosis IPF 59 Osteoarthritis OA 59 retinal dysfunction 59 Lennox Gastaut Syndrome 59 sporadic ALS 59 irreversible blindness 59 tremors rigidity 59 NPHP 59 Usher Syndrome 59 Sensorineural hearing loss 59 Prosopagnosia 59 retinitis pigmentosa RP 59 gene APOE4 59 Von Hippel Lindau 59 LRP5 59 Pelizaeus Merzbacher disease 59 hypotonia 59 susceptibility gene 59 Metastases 59 neuro degenerative disorders 59 Ischaemic heart 59 Epidermolysis bullosa 59 Stress urinary incontinence 59 1 Antitrypsin Deficiency 59 endocrine disorder 59 Cancer cachexia 59 neurobehavioral disorders 59 Ectodermal Dysplasia 59 Janus kinase 59 Hemiplegia 59 hereditary hemorrhagic telangiectasia 59 Autistic Disorder 59 chorea associated 59 Lou Gehrigs disease 59 urethritis 59 IL#R 59 cardiac hypertrophy 59 Insulin resistance 59 syndrome FXTAS 59 seizures comas 59 Sarcopenia 59 tic disorder 59 neurologic disorders 59 Vitamin D insufficiency 59 Compulsive hoarding 59 ADAMTS# 59 severe dehydrating diarrhea 59 bullous 59 Thyroid disorders 59 superior mesenteric artery 59 myotonia 59 erythematosus 59 Apraxia 59 generalized seizures 59 WDR# 59 familial adenomatous polyposis FAP 59 epiglottitis 59 TTR FAP 59 MELAS syndrome 59 Duchenne muscular dystrophy DMD 59 pigmentosa 59 Diabetes mellitus 59 FMR1 gene 59 Benign prostatic hyperplasia 59 eosinophilic 59 axonal damage 59 Lactose intolerance 59 hyperprolactinemia 59 Dravet Syndrome 59 Borderline personality 59 hemorrhagic colitis 59 obliterans 59 Postpartum psychosis 59 velo cardio facial 59 kidney urologic 59 Cerebellar 59 muscle degeneration 59 neurologic symptoms 59 eosinophilic esophagitis 59 Hurler syndrome 59 Periodontal disease 59 Beta thalassemia 59 malignant fibrous histiocytoma 59 FXTAS 59 Duchenne Becker 59 Peanut allergy 59 genetic disorder 59 Peripheral arterial disease 59 LRRK2 mutations 59 juvenile myoclonic epilepsy 59 LRRK2 gene 59 essential thrombocythemia 59 Neuronal 59 Transverse Myelitis 59 Parkinson disease neurological disorder 59 lupus erythematosus 59 Raynaud disease 58 Epileptic seizures 58 Acromegaly 58 Fecal incontinence 58 chronic rheumatic 58 interferon pathway 58 hyperplastic 58 Stargardt Macular Dystrophy 58 dizziness imbalance 58 JAK mutations 58 uncontrollable shaking 58 PCNSL 58 Relapsing remitting 58 Autism Asperger Syndrome 58 gastro esophageal reflux 58 Gestational diabetes 58 SCN5A 58 diffuse intrinsic pontine glioma 58 Dental fluorosis 58 Severe sepsis 58 myelodysplasia 58 mutated protein 58 mitochondrial myopathy 58 microcephalin 58 acquired immunodeficiency syndrome 58 arterial calcification 58 discoid lupus 58 Lou Gherig Disease 58 chronic degenerative 58 genus Plasmodium 58 PKU genetic 58 Immune Deficiency 58 Genetic Variations 58 KCNH2 58 Parkinsonian 58 cause cardiac channelopathies 58 Myocardial infarction 58 lysosomal diseases 58 Pituitary 58 SHANK3 58 Aortic dissection 58 Hemochromatosis 58 insulin resistance syndrome 58 VCFS 58 HELLP 58 lissencephaly 58 Creutzfeld Jakob disease 58 Pericarditis 58 cutaneous lesions 58 Tourette Syndrome neurological disorder 58 dystrophies 58 neuroblastomas 58 Sandhoff disease 58 Abdominal aortic aneurysms 58 Genes Linked 58 Myelofibrosis 58 muscle rigidity 58 Perennial allergic rhinitis 58 dentinal hypersensitivity 58 Obsessive Compulsive Disorder OCD 58 dysregulation 58 Chronic lymphocytic leukemia CLL 58 Recurrences 58 Anencephaly 58 opportunistic viral infection 58 Undiagnosed 58 Arrhythmias 58 atypical parkinsonism 58 Schizophrenia affects 58 PNET 58 Mitochondrial 58 monocytic 58 regulator CFTR gene 58 common neurovascular complication 58 Polycystic Ovary Syndrome 58 Diabetic peripheral neuropathy 58 Cirrhosis 58 astrocytomas 58 Cognitive Deficits 58 carcinoid tumors 58 Fanconi anemia 58 Nephrogenic Systemic Fibrosis NSF 58 chronic relapsing 58 Six3 58 Multiple myeloma 58 prosopagnosia 58 ATTR PN 58 Autoimmune hepatitis 58 Wegener Granulomatosis 58 Benign Paroxysmal Positional Vertigo 58 meningitis encephalitis 58 Wernicke Korsakoff syndrome 58 Dystonia 58 spasmodic dysphonia 58 ARVD 58 Subtype 58 hyperparathyroidism 58 Prostatitis 58 hyperactivation 58 Social Phobia 58 muscular spasticity 58 erythema nodosum 58 Glucocorticoid 58 neurogenetic 58 Excessive daytime sleepiness 58 Sydenham chorea 58 underlying pathophysiology 58 nasopharyngeal carcinoma 58 Alzheimer disease cognitive impairment 58 lymphoblastic lymphoma 58 Persistent Sexual Arousal 58 Parkinson disease multiple sclerosis 58 temporomandibular joint disorder 58 Parkinson disease neurodegenerative disorder 58 juvenile dermatomyositis 58 myelogenous leukemia 58 hyperexcitability 58 Gene Mutations 58 Chronic fatigue syndrome 58 Lennox Gastaut syndrome 58 Moraxella catarrhalis 58 Gastric cancer 58 trophoblastic 58 alexia 58 Oxidative stress 58 colorectal carcinoma 58 osteoarthritis degenerative 58 Chronic hepatitis B 58 arrhythmogenic 58 MTHFR 58 MLL2 58 syringomyelia 58 idiopathic epilepsy 58 neurological abnormalities 58 Von Willebrand 58 parkin gene 58 dysphasia 58 disorder characterized 58 Meckel Gruber 58 neuritis 58 Autoimmune diseases 58 Creutzfeldt Jacob 58 polyneuropathy 58 Glioblastomas 58 Sjogren Syndrome 58 myofascial pain syndrome 58 carcinoid 58 Rett syndrome 58 Infant botulism 58 Chronic rhinosinusitis 58 progressive retinal degenerative 58 Mild cognitive impairment 58 Escherichia coli Klebsiella pneumoniae 58 Chronic cough 58 Chemotherapy induced 58 aMCI precursor 58 Metastatic breast cancer 58 Extensively drug 58 Protein Linked 58 Tardive dyskinesia 58 juvenile myelomonocytic leukemia 58 chronic obstructive airway 58 Chronic HCV 58 X Chromosome 58 Cystic fibrosis 58 Alport Syndrome 58 Dysregulation 58 Chronic inflammation 58 Nephrogenic 58 arrhythmogenic right 58 gliosis 58 MAP#K# 58 congenital deafness 58 late infantile neuronal 58 nonhereditary 58 spastic colon 58 neuroendocrine 58 Genetic predisposition 58 Prion diseases 58 Cardiac hypertrophy 58 septo optic dysplasia 58 Glioblastoma multiforme 58 retinal dystrophy 58 Pemphigus 58 Lymphocytic 58 desmoplastic 58 Schizoaffective disorder 58 dystonia neurological movement 58 Major Depressive 58 chromosomal disorders 58 chronic idiopathic 58 Polycystic Kidney Disease 58 included exfoliative dermatitis 58 predisposing factor 58 Acute Myelogenous Leukemia 58 Loeys Dietz syndrome 58 Hirschsprung disease 58 Neural tube defects 58 hay fever allergic rhinitis 58 xeroderma pigmentosum 58 Huntington Chorea 58 Huntingtin 58 Gorlin syndrome 58 Panic Disorder 58 Wolf Hirschhorn 58 lateral sclerosis ALS 58 cognitive dysfunctions 58 Rheumatic fever 58 Ventricular Tachycardia 58 C1 INH deficiency 58 intestinal inflammation 57 BCL#A 57 Menkes disease 57 KCNQ1 57 NASH Huntington 57 infection progressive multifocal 57 chronic lymphocytic 57 Spinal cord injuries 57 Behcet syndrome 57 gastrointestinal stromal tumor 57 metabolic abnormality 57 gastrointestinal reflux 57 multiple endocrine neoplasia 57 blindness paralysis 57 pathological hallmarks 57 Gene Mutation Linked 57 chromosomal rearrangement 57 disorder ASD 57 paroxysmal nocturnal hemoglobinuria 57 Polyneuropathy 57 β thalassemia 57 deCODE Glaucoma TM 57 degenerative disorders 57 BRCA1 BRCA2 57 paralytic illness 57 Polycystic Ovarian Syndrome PCOS 57 Decompensated 57 Encephalopathy 57 Genetic Variation 57 Fanconi anemia FA 57 MeCP2 gene 57 gastroenteritis conjunctivitis 57 Duchene muscular dystrophy 57 sustained muscle contractions 57 Osteogenesis Imperfecta 57 basal forebrain 57 Irritable Bowel Syndrome IBS 57 cerebellar hypoplasia 57 bacterium Mycobacterium leprae 57 chaotic heartbeats 57 mitochondrial disorders 57 Acute sinusitis 57 Folate deficiency 57 proliferative diabetic retinopathy 57 SRBD 57 Hemolytic Uremic Syndrome 57 hematological abnormalities 57 lactose malabsorption 57 roseola 57 congenital anomaly 57 Variant CJD 57 developmental abnormalities 57 Gene Mutation 57 alveolar rhabdomyosarcoma 57 Sezary syndrome 57 Keratitis 57 Nausea vomiting 57 juvenile idiopathic arthritis 57 coagulopathy 57 epidermolysis bullosa EB 57 Ebola Hemorrhagic Fever 57 epithelioid 57 Lymphomas 57 #beta HSD1 57 bradykinesia 57 deafness neurological 57 neuropathologic 57 neuropsychiatric diseases 57 immunocompetent 57 fungus Cryptococcus neoformans 57 Neurogenic 57 Lou Gherig disease 57 atrophic gastritis 57 hepatic cirrhosis 57 NOD2 57 Shows Promise Against 57 Shwachman Diamond Syndrome 57 narcolepsy cataplexy 57 cardiomyopathy weakening 57 neuritic 57 progressive neurologic 57 Osteopenia 57 protein misfolding 57 dysautonomia