Related by context. All words. (Click for frequent words.) 70 progressive neurodegenerative disorder 69 dominantly inherited 69 monogenic 69 missense mutations 68 inflammatory demyelinating 68 myoclonus 68 Leber hereditary optic neuropathy 68 neurodegenerative disorder 68 epilepsies 68 anemias 68 myopathies 68 neurological manifestations 68 Brugada syndrome 67 Prion diseases 67 autosomal recessive 67 Neurodegenerative diseases 67 inherited mutations 67 parkinsonism 67 Parkinsonian Syndromes 67 ADPKD 67 de novo mutations 67 Brugada Syndrome 67 LRRK2 mutations 66 autosomal dominant disorder 66 hereditary predisposition 66 paraneoplastic 66 immunodeficiencies 66 susceptibility gene 66 genetic loci 66 Essential tremor 66 PTPN# 66 inherited neurological disorder 66 GBA mutations 65 neurological disorder affecting 65 Hashimoto thyroiditis 65 FTLD 65 sCJD 65 fatal neuromuscular disorder 65 ANCA associated 65 progressive neurodegenerative 65 motor neuron degeneration 65 Myotonic dystrophy 65 familial ALS 65 inherited retinal degeneration 65 vascular cognitive impairment 65 euthymic patients 65 aneuploidies 65 Diabetic neuropathy 65 parkinsonian 65 TTR amyloidosis 65 myalgias 65 neurologic disorders 65 fronto temporal dementia 65 lichen planus 65 mtDNA mutations 65 autosomal dominant polycystic kidney 65 autosomal dominant 64 neoplastic diseases 64 predisposing factor 64 gene MECP2 64 ataxia 64 #q#.# [001] 64 multisystem disease 64 Systemic lupus erythematosus SLE 64 Sjögren syndrome 64 systemic autoimmune 64 bullous 64 modifier genes 64 incurable neurological disorder 64 alpha synuclein protein 64 Systemic lupus erythematosus 64 chromosomal rearrangement 64 neurofibromas 64 muscle rigidity 64 etiologies 64 systemic amyloidosis 64 muscular dystrophies 64 neuronal dysfunction 64 ciliopathies 64 Parkinsonian 64 oculomotor 64 mitochondrial disorders 64 myeloproliferative 64 nonhereditary 64 Li Fraumeni syndrome 64 CHD7 64 hay fever allergic rhinitis 64 neuroblastomas 64 Leukemias 64 optic atrophy 64 Chronic pancreatitis 64 Genetic predisposition 64 Eisenmenger syndrome 64 generalized epilepsy 64 underlying pathophysiology 63 debilitating neurodegenerative disorder 63 Genetic variants 63 allelic variants 63 gliosis 63 idiopathic PAH 63 behavioral abnormalities 63 LRRK2 gene 63 encephalitis meningitis 63 progressive degenerative neurological 63 Henoch purpura 63 autoinflammatory diseases 63 neurologic disorder 63 hypometabolism 63 meningitis encephalitis 63 cystic fibrosis Duchenne muscular 63 incurable neurodegenerative disease 63 CDH1 63 paragangliomas 63 Hypophosphatasia 63 motor neuron diseases 63 Genetic mutations 63 Sydenham chorea 63 neurosensory 63 unprovoked seizures 63 necrotizing 63 SCN5A 63 Korsakoff syndrome 63 Hypertrophic 63 myelofibrosis polycythemia vera 63 degenerative disorders 63 sporadic ALS 63 herpesviruses 63 Autoimmune disorders 63 neuritic 63 FXTAS 63 chronic autoimmune disorder 63 neurological abnormalities 63 Bardet Biedl Syndrome 63 Polymorphic Ventricular Tachycardia CPVT 63 microdeletion 63 Epstein Barr virus EBV 63 alexithymia 63 childhood disintegrative disorder 63 neurodegenerative disorder characterized 63 Hutchinson Gilford progeria 63 severe malignant osteopetrosis 63 coagulopathy 63 metabolic abnormality 63 MGUS 63 lateral sclerosis ALS 63 IL#R 63 genetically inherited 63 Cerebellar 63 lupus scleroderma 63 familial clustering 63 lymphocytic 63 Von Willebrand disease 63 astrocytic 63 granulomatous 63 Aortic stenosis 63 hamartomas 62 dysgenesis 62 Dilated cardiomyopathy 62 susceptibility alleles 62 fibrosing 62 tremor rigidity 62 torsade de pointes 62 sporadic Creutzfeldt Jakob 62 V#F mutation 62 AAT Deficiency 62 autosomal recessive genetic 62 chromosome #q#.# [001] 62 lysosomal storage disease 62 Neurofibromatosis type 62 complement inhibitor eculizumab 62 chromosomal anomalies 62 hyperexcitability 62 tremors slowness 62 demyelinating disease 62 familial pancreatic cancer 62 neuropsychological impairments 62 hereditary spastic paraplegia 62 Hurthle cell 62 dyskeratosis congenita 62 causative genes 62 recessive trait 62 polymyalgia rheumatica 62 autosomal recessive disorder 62 Shy Drager syndrome 62 neurologic symptoms 62 nongenetic 62 transgenic mouse models 62 EBV infection 62 Tourette Syndrome TS 62 neurological disorder characterized 62 Magnesium deficiency 62 Myasthenia gravis 62 Hereditary angioedema 62 Churg Strauss syndrome 62 DQB1 * 62 essential thrombocythemia 62 Cryptococcus neoformans 62 inherited genetic mutations 62 recessive genetic 62 myelopathy 62 rheumatoid arthritis lupus 62 Treg cell 62 endophenotypes 62 glomerulonephritis 62 JAK2 mutation 62 facioscapulohumeral muscular dystrophy 62 VHL gene 62 Cowden syndrome 62 #q#.# [002] 62 optic neuropathy 62 epigenetic alterations 62 hyperprolactinemia 62 OSAHS 62 primary ciliary dyskinesia 62 neoplastic 62 neurodevelopmental disorder 62 autonomic dysfunction 62 MYH9 gene 62 gene polymorphisms 62 cortical dysplasia 62 alpha thalassemia 62 DNA methylation patterns 62 cause cardiac channelopathies 62 Leydig cell 62 TCF#L# 62 KCNH2 62 eosinophilic 62 postural instability 62 spinocerebellar ataxia 62 pathophysiologic 62 genes predisposing 62 SSc 62 polyglutamine diseases 62 Pulmonary hypertension 62 G#S [002] 62 chromosomal deletions 62 osteosarcomas 62 astrocytomas 62 Proteus syndrome 62 JAK2 enzyme 62 pilocytic astrocytomas 62 degenerative neurological diseases 62 Arrhythmogenic 62 chronic obstructive airway 62 myotonia 62 dystonias 62 methicillin susceptible Staphylococcus aureus 62 atrophic gastritis 62 dystrophies 62 arthritis RA 62 Keratitis 61 NF1 61 ataxic 61 functional polymorphism 61 familial adenomatous polyposis 61 hyperinsulinism 61 thalassemia sickle cell 61 neuropsychiatric diseases 61 MECP2 gene 61 pain syndromes 61 inappropriate antidiuretic hormone SIADH 61 hypothalamic pituitary adrenal axis 61 chromosome #q# [001] 61 Atopic dermatitis 61 APOE ε4 61 torsion dystonia 61 hypoperfusion 61 variable immunodeficiency 61 hydrops 61 genetic syndromes 61 demyelination 61 PTEN mutations 61 TP# mutation 61 hyperplastic 61 causative mutations 61 Childhood Disorder 61 mental retardation epilepsy 61 leukoencephalopathy 61 polyneuropathy 61 muscular dystrophy cystic fibrosis 61 systemic scleroderma 61 pathological hallmark 61 microcephalin 61 hematological abnormalities 61 neuro degenerative disorders 61 clefting 61 benign positional vertigo 61 supratentorial 61 germline mutations 61 bone marrow mesenchymal stem 61 TACI mutations 61 Inflammatory bowel diseases 61 metaplasia 61 IgA deficiency 61 untreated celiac disease 61 phenotypes 61 Streptococcus pneumoniae Haemophilus influenzae 61 neuropsychiatric disorder 61 missense mutation 61 oligodendrogliomas 61 predisposing factors 61 susceptibility loci 61 Aspergillus species 61 dissociative disorders 61 Ischaemic heart 61 tonic clonic seizures 61 Leber Hereditary Optic Neuropathy 61 lysosomal storage diseases 61 hereditary degenerative 61 Clinical manifestations 61 Trichophyton rubrum 61 autonomic neuropathy 61 Ribavirin causes 61 maternally inherited 61 sphingolipid 61 Arrhythmogenic Right Ventricular Cardiomyopathy 61 genetic polymorphisms 61 Squamous 61 cypin 61 HNPCC 61 autoimmune thyroid 61 Dysregulation 61 spinocerebellar ataxia type 61 myeloproliferative neoplasms 61 autosomal recessive disease 61 hypercoagulable 61 paresis 61 idiopathic pulmonary 61 neurofibroma 61 encephalomyelitis 61 Beta thalassemia 61 disabling neurological 61 post transplant lymphoproliferative 61 hypotonia 61 Parkinson Disease PD 61 degenerative disorder 61 etiologic 61 ABCB1 gene 61 M. pneumoniae 61 atypical parkinsonism 61 locus coeruleus 61 rheumatic disease 61 pulmonary hypertension PH 61 myasthenia gravis MG 61 neoplasias 61 Mycoplasma pneumoniae 61 AAT deficiency 61 biochemical abnormalities 61 Cognitive impairment 61 bradykinesia 61 airway hyperresponsiveness 61 Epstein Barr Virus 61 neuroinflammation 61 flaccid paralysis 61 Chronic lymphocytic leukemia 61 gastric carcinoma 61 ataxia telangiectasia 61 tauopathies 61 metabolic abnormalities 61 degenerative neurological condition 61 rare autosomal recessive 61 Alzheimer disease vascular dementia 61 chromosome #q#.# [002] 61 demyelinating diseases 61 genetic lysosomal storage 61 Becker muscular dystrophy 61 myalgic encephalomyelitis ME 61 Metastases 61 microdeletions 61 neuropsychiatric disorders 61 clinically heterogeneous 61 susceptibility genes 61 SMAD4 61 gene locus 61 Vitamin D insufficiency 61 ependymomas 61 HLA B# 61 epilepsy Parkinson disease 61 Sporadic CJD 61 cerebellar 60 circadian genes 60 filaggrin 60 G6PD deficiency 60 arterial calcification 60 neuro degenerative disorder 60 tremor slowness 60 hyperreflexia 60 underlying vasculopathy 60 choroidal neovascularization 60 autoinflammatory 60 arthropathy 60 hyperalgesia 60 neuro developmental disorder 60 antiphospholipid syndrome 60 #p#.# [002] 60 respiratory gastrointestinal 60 Bullous 60 ectodermal dysplasia 60 MLH1 60 hemoglobinopathies 60 agnosia 60 ORMDL3 60 ABCB1 60 Cystic fibrosis CF 60 frontotemporal dementia 60 enterocolitis 60 leiomyoma 60 affective psychosis 60 CYP#A# gene 60 spontaneous mutations 60 hereditary hemochromatosis 60 SOD1 gene 60 MSH2 60 carcinoids 60 neurologic complications 60 Idiopathic 60 holoprosencephaly 60 hormonal abnormalities 60 meningiomas 60 LRAT 60 NPHP 60 Lewy body 60 autosomal dominant inheritance 60 nonprogressive 60 p# activation 60 Hyperthyroidism 60 Legg Calvé Perthes disease 60 nondemented 60 Angelman syndrome 60 cutaneous lesions 60 COL#A# 60 incomplete penetrance 60 Hemorrhagic 60 isotypes 60 Pervasive Developmental Disorder 60 myelomas 60 chronic degenerative 60 extrapyramidal symptoms 60 thyrotoxicosis 60 cardiac channelopathies 60 methylenetetrahydrofolate reductase 60 neuropathies 60 renal diseases 60 eccrine 60 SLC#A# [002] 60 Peripheral neuropathy 60 Alzheimer disease cognitive impairment 60 neuro degenerative disease 60 periventricular 60 Retinitis pigmentosa 60 hypokalemia hypomagnesemia 60 apolipoprotein E gene 60 polymorphic ventricular tachycardia 60 Tay Sachs thalassemia 60 osteochondromas 60 NR#A# 60 Dwarfism 60 anatomical abnormalities 60 Cushing syndrome 60 Peutz Jeghers syndrome 60 epigenetically 60 nerve degeneration 60 obesity insulin resistance 60 endocannabinoid signaling 60 Bronchiolitis 60 Vitamin B# deficiency 60 chronicity 60 chromosome #p#.# 60 progressive dyspnea 60 neurocysticercosis 60 myotonic dystrophy 60 neuropathologic 60 haemorrhagic 60 erythematosus 60 viral etiology 60 neuritis 60 HbF 60 arteriovenous malformations 60 MYH9 60 Thyroid disorders 60 hemorrhagic colitis 60 somatic mutation 60 WNK1 60 impaired cognition 60 fungoides 60 LHON 60 virulence genes 60 phonic tics 60 nephronophthisis 60 bronchogenic carcinoma 60 Muscular dystrophies 60 motor tics 60 MELAS 60 idiopathic myelofibrosis 60 SNCA 60 Entamoeba histolytica 60 Alleles 60 allele frequencies 60 huntingtin gene 60 Nonspecific 60 spongiform encephalopathies 60 cryptogenic 60 motor neuropathy 60 recessive inheritance 60 discoid lupus 60 Dysplasia 60 MTHFR 60 severe obstructive pulmonary 60 R#W [002] 60 arrhythmogenic 60 renal fibrosis 60 degenerative neurological disorder 60 atypical hemolytic uremic syndrome 60 generalized vitiligo 60 Multiple sclerosis MS 60 obstructive sleep 60 beta globin gene 60 progressive degenerative 60 genomic variants 60 channelopathies 60 synovial cells 60 TCF#L# gene 60 Hip dysplasia 60 periventricular leukomalacia 60 amyloid deposition 60 extrapyramidal 60 paralogs 60 Polyneuropathy 60 primary hyperparathyroidism 60 Lewy bodies 60 aetiology 60 Bardet Biedl syndrome 60 synaptic function 60 polymyalgia 60 non coding RNA 60 glial tumors 60 von Hippel Lindau 60 vWD 60 polyuria 60 paraganglioma 60 proliferative diabetic retinopathy 60 demyelinating disorders 60 thyroid dysfunction 60 Moraxella catarrhalis 60 vivax 60 NOD2 60 basal cell nevus syndrome 60 pathogenic mechanisms 60 anosognosia 60 somatic mutations 60 kidney urologic 60 Polymorphisms 60 hematologic disorders 60 phenotypic expression 60 genetic polymorphism 60 epithelial tumors 60 akinesia 60 hypermethylated 60 Haptoglobin 60 mucocutaneous 60 Acute Bacterial Sinusitis ABS 60 karyotypes 60 infarcts 60 fatal neurodegenerative disorder 60 encephalitis swelling 60 haematopoietic 60 glutamic acid decarboxylase 60 Osteogenesis imperfecta 60 dysthymic disorder 60 5 HT1A 60 carcinoid 60 multi factorial disease 60 HLA DRB1 * 60 Wernicke Korsakoff syndrome 60 K ras mutations 60 Meckel Gruber 60 unknown etiology 60 neural crest 60 pathophysiological mechanisms 59 respiratory viral infections 59 Atypical antipsychotics 59 comorbid disorders 59 constitutively expressed 59 genetic determinants 59 primary progressive aphasia 59 Sezary syndrome 59 hypothalamic pituitary 59 syndromic 59 Psoriatic arthritis 59 Sjogren Syndrome 59 trigeminal 59 cardiomyopathies 59 genus Plasmodium 59 hyper IgE syndrome 59 neoplasm 59 T#M 59 #q# [001] 59 lupus multiple sclerosis 59 hypogonadotropic hypogonadism 59 leiomyomas 59 rheumatic disorders 59 PAOD 59 striatal neurons 59 CNTNAP2 59 TTR gene 59 tics involuntary 59 esophageal squamous cell carcinoma 59 Gorlin syndrome 59 seminomas 59 nonalcoholic steatohepatitis NASH 59 narcolepsy cataplexy 59 dermatophytes 59 Meckel Gruber syndrome 59 oral thrush 59 neurological dysfunction 59 Gliomas 59 cAMP signaling 59 muscular stiffness 59 recessively inherited 59 HLA DRB1 59 LVNC 59 metastatic neuroendocrine tumors 59 monozygotic twin 59 staphylococcal infections 59 interstitial pneumonitis 59 neurogenic 59 developmental abnormalities 59 germline mutation 59 hypovitaminosis D 59 induce orthostatic hypotension 59 Retinitis Pigmentosa RP 59 interstitial fibrosis 59 Vascular dementia 59 KRAS oncogene 59 CP CPPS 59 A. fumigatus 59 Idiopathic pulmonary fibrosis IPF 59 sclerosis ALS 59 dysphasia 59 chromosomal aberrations 59 protein misfolding diseases 59 SCN1A 59 multiforme 59 affective psychoses 59 syndrome gastroesophageal reflux 59 differential gene expression 59 glucocorticoid receptors 59 ApoE gene 59 fatal myelination disorder 59 BMPR2 59 KCNQ1 59 neutropenia thrombocytopenia 59 mucinous 59 Nonalcoholic fatty liver 59 myelination disorders 59 involuntary tics 59 EoE 59 subcortical 59 Iron deficiency anemia 59 PsA 59 Atopic eczema 59 autoimmune thyroiditis 59 demyelinating 59 dementia praecox 59 genomic deletions 59 SOD1 mutation 59 BRAF V#E 59 CYT# potent vascular disrupting 59 L. pneumophila 59 phenotypic differences 59 mucus glands 59 Raynaud syndrome 59 secondary bacterial infections 59 haematologic 59 arrhythmogenic right 59 idiopathic generalized epilepsy 59 Parkinsonism 59 mitochondrial mutations 59 Irritable bowel syndrome 59 inhibitory transmitter 59 Juvenile Idiopathic Arthritis JIA 59 NF1 gene 59 mGluR 59 activating mutation 59 CCR5 delta# 59 Purkinje cells 59 dopamine signaling 59 Lou Gehrigs disease 59 hypercalcaemia 59 lupus erythematosus 59 mycosis fungoides 59 Alport syndrome 59 amnestic 59 pituitary adenomas 59 MYCN amplification 59 temporal arteritis 59 Celiac sprue 59 Kufs disease 59 mosaicism 59 Alzheimer Disease AD 59 deafness blindness 59 epithelioid 59 disorder characterized 59 neuro developmental disorders 59 mitochondrial dysfunction 59 Periodontitis 59 IgA nephropathy 59 polymicrobial infections 59 necrotising 59 Idiopathic pulmonary fibrosis 59 chromosome rearrangements 59 acute porphyria 59 nucleoli 59 Endometrial cancer 59 Trypanosoma 59 Irritable bowel syndrome IBS 59 Huntingtons disease 59 Lafora disease 59 Huntington chorea 59 neuroligins 59 receptor subtypes 59 apoE4 59 LRP5 59 p# mutations 59 humans variant Creutzfeldt 59 genetic heterogeneity 59 KIF6 gene 59 Spasticity 59 ischemic optic neuropathy 59 congenital disorders 59 genes differentially expressed 59 neuropathic pain spasticity 59 artery stenosis 59 Fibroblasts 59 schizotypal 59 debilitating autoimmune 59 Parkinsons disease 59 KIBRA 59 pseudotumor cerebri 59 BH4 deficiency 59 mental retardation cerebral palsy 59 CYP#C# gene 59 Zinc deficiency 59 parkin gene 59 autoimmune encephalitis 59 anemia thrombocytopenia 59 familial aggregation 59 multigenic 59 bullous pemphigoid 59 ERK signaling 59 1 diabetes T1D 59 dysregulated 59 phenotypic variation 59 neurofibrillary 59 Viral infections 59 amyloid cascade 59 C1q 59 Neisseria 59 TMEM#B 59 susceptibility locus 59 cognitive dysfunctions 59 disorders FASD 59 non syndromic 59 recurrent laryngeal nerve 59 monozygotic twins 59 Prefrontal 59 GABRA2 59 gene rearrangements 59 lymphoid cells 59 gastric adenocarcinoma 59 #p#.# [001] 59 gastrointestinal disturbances 59 meningeal 59 NFTs 59 pleiotropic effects 59 leaky gut 59 erythema nodosum 59 microvascular disease 59 cystic fibrosis chronic pancreatitis 59 β thalassemia 59 monoclonal gammopathy 59 primary biliary cirrhosis 59 gastric carcinomas 59 obstructive coronary 59 dysplasias 59 synovial fibroblasts 59 SHANK3 gene 59 inhibitory neurotransmitters 59 Prostatitis 59 N. gonorrhoeae 59 neuroleptic malignant syndrome 59 pulvinar 59 HER2 overexpression 59 lymph node enlargement 58 skeletal muscle weakness 58 diarrhea predominant IBS 58 neurologic diseases 58 thrombocytosis 58 alpha synuclein gene 58 ALK mutations 58 progressive degeneration 58 glutamatergic 58 included exfoliative dermatitis 58 Lymphoid 58 hyperparathyroidism 58 Spinal muscular atrophy 58 prodrome 58 benign paroxysmal positional vertigo 58 schizotypal traits 58 Hemangiomas 58 Panton Valentine leukocidin PVL 58 pathophysiological effects 58 nasal stuffiness 58 homozygous FH 58 Autoimmune hepatitis 58 sickle cell cystic fibrosis 58 Graves ophthalmopathy 58 sonographic appearance 58 fibrotic disease 58 familial hypercholesterolemia 58 pathophysiological 58 blindness paralysis 58 Genital herpes 58 immunocompetent 58 Pseudomonas syringae 58 calculi 58 tau pathology 58 Fungal infections 58 immuno deficiency 58 Dental fluorosis 58 nonsense mutations 58 Helicobacter 58 schwannomas 58 basal forebrain 58 protein tyrosine phosphatase 58 hypercoagulability 58 #q# deletion 58 Upregulation 58 congenital anomaly 58 heterozygotes 58 paralysis blindness 58 dermopathy 58 sclerosing 58 radiographic findings 58 mGluR5 antagonist 58 Urinary tract 58 APOL1 58 myofascial pain syndrome 58 Hurler syndrome 58 muscle spasticity 58 achromatopsia 58 causal variants 58 Chronic constipation 58 myoclonic epilepsy 58 Sleep disordered breathing 58 cardiac conduction 58 GLUT1 58 colic diarrhea 58 promoter hypermethylation 58 syndrome OSAS 58 gene deletions 58 Autistic Disorder 58 dysbindin 58 leptin deficiency 58 neurofibromatosis type 58 capillary leak 58 orchitis 58 Autoimmune diseases 58 Ischemic 58 multi infarct dementia 58 Parkinson disease multiple sclerosis 58 hyperglycaemia 58 hypereosinophilic syndrome 58 IPAH 58 Eosinophilic 58 SGPT 58 comorbid depression 58 primidone 58 apolipoprotein E APOE 58 bacterium Neisseria meningitidis 58 chronic eosinophilic leukemia 58 rhinorrhea 58 mesenteric 58 BRAF gene 58 HSV1 58 tumoral 58 cramping abdominal pain 58 neuronal plasticity 58 dystrophy 58 hypomethylation 58 retinal blindness 58 Mendelian disorders 58 gastric distention 58 Medulloblastoma 58 hippocampal function 58 primary aldosteronism 58 ADAMTS# 58 Chlamydia pneumoniae 58 distinct subtypes 58 neurogenetic 58 serine proteases 58 pathological hallmarks 58 Skeletal muscle 58 pathogenic mutations 58 disorders 58 hemolytic anemia 58 Congenital Muscular Dystrophy 58 von Willebrand 58 glycolipids 58 papular 58 gamma oscillations 58 Nephrogenic Systemic Fibrosis NSF 58 tissue fibrosis 58 chromosomal regions 58 Abeta protein 58 frontotemporal 58 spinal muscle atrophy 58 Alzheimer disease frontotemporal dementia 58 chronic lymphocytic 58 Epstein Barr Virus EBV 58 tardive dyskinesia TD 58 cystic kidney 58 giant cell arteritis 58 TSC1 58 lysosomal 58 dermatologic reactions 58 alpha1 antitrypsin deficiency 58 normal karyotype 58 imperfecta 58 Clusterin 58 syndromes 58 osteopetrosis 58 axonal damage 58 synaptogenesis 58 HG PIN 58 cytopenia 58 papillomas 58 genes encode proteins 58 immunodeficiency disorder 58 enteroviruses 58 pancreatic endocrine 58 promoter polymorphism 58 MEF2A 58 proliferative disorders 58 pituitary tumors 58 perivascular 58 pancytopenia 58 torticollis 58 diabetic microvascular complications 58 Parkinson degenerative 58 progressive neurodegenerative disease 58 Glioblastoma Multiforme GBM 58 Hereditary angioedema HAE 58 PCNSL 58 nasopharyngeal carcinoma 58 inherited retinal 58 retinitis pigmentosa RP 58 myeloproliferative diseases 58 atopic 58 neurocognitive impairment 58 urticaria hives 58 dysphonia 58 hyperammonemia 58 endocrine tumors 58 Basal cell 58 Escherichia coli Klebsiella pneumoniae 58 Polycythemia 58 progressive neurodegenerative disorders 58 aniridia 58 hypochondriasis 58 C. neoformans 58 plexiform 58 bacterial prostatitis 58 thrombocytopenia neutropenia 58 multisystemic 58 Lewy bodies DLB 58 CYP #A# 58 Diabetic nephropathy 58 malignant lymphomas 58 Uncontrolled diabetes 58 folate metabolism 58 Candida infection 58 ocular inflammatory 58 Social Phobia 58 LMNA 58 olfactory dysfunction 58 suppurative 58 Paroxysmal 58 Transverse myelitis 58 white matter hyperintensities 58 schwannoma 58 polydipsia 58 Htt 58 embryonal rhabdomyosarcoma 58 somatic complaints 58 hypocalcaemia 58 LQTS 58 VCFS 58 SE alleles