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(Click for frequent words.) 64 Hutchinson Gilford progeria 64 imperfecta 62 Hutchinson Gilford Progeria 61 dyskeratosis congenita 60 fronto temporal dementia 60 velo cardio facial 60 recessive dystrophic epidermolysis bullosa 60 autosomal dominant disorder 60 autoinflammatory diseases 60 sporadic Creutzfeldt Jakob 60 nerve degeneration 60 Becker muscular dystrophy 60 paraganglioma 60 brain malformation 60 osteopetrosis 59 hereditary spastic paraplegia 59 Brugada syndrome 59 Kufs disease 59 neurologic disorder 59 Lafora disease 59 Fanconi Anemia 59 primary ciliary dyskinesia 59 Myocarditis 59 myelopathy 59 inherited neurological disorder 59 progressive neurodegenerative disorder 59 autosomal recessive disease 59 Dysplasia 59 chromosome abnormality 59 Arrhythmogenic Right Ventricular Cardiomyopathy 59 mastocytosis 59 Osteogenesis imperfecta 59 motor neuron degeneration 58 Cockayne syndrome 58 lysosomal storage disease 58 Epstein Barr Virus 58 Niemann Pick disease 58 causative gene 58 thyroid hormone deficiency 58 multisystem disease 58 1 Antitrypsin Deficiency 58 leptin deficiency 58 Amyotrophic lateral sclerosis 58 progressive neurodegenerative 58 Li Fraumeni syndrome 58 Leber congenital amaurosis 58 autosomal recessive disorder 58 Duchenne Becker 58 sporadic ALS 58 hemophagocytic lymphohistiocytosis 58 Wolf Hirschhorn 58 pathological hallmark 58 neurodegenerative disorder 58 alpha1 antitrypsin deficiency 58 von Hippel Lindau 58 NKX2 58 pseudotumor cerebri 58 Loeys Dietz syndrome 57 nodular lesions 57 polymyalgia rheumatica 57 myopathies 57 neuropsychiatric disorder 57 thoracic aortic aneurysm 57 Acute Myelogenous Leukemia 57 fatal neuromuscular disorder 57 Spinal muscular atrophy 57 polycystic kidneys 57 systemic amyloidosis 57 autosomal recessive genetic 57 MELAS 57 chronic autoimmune disorder 57 neurological disorder affecting 57 Brugada Syndrome 57 neuronal dysfunction 57 myositis 57 Neurofibromatosis type 57 Hutchinson Gilford Progeria Syndrome 57 incurable neurological disorder 57 postural orthostatic tachycardia 57 superior mesenteric artery 57 motor neurone 57 NPHP 57 amyloid protein plaques 57 retinal dysfunction 57 Lesch Nyhan syndrome 57 myelogenous leukemia 57 fatal neurodegenerative disorder 57 myotonic muscular dystrophy 57 Pelizaeus Merzbacher disease 57 post transplant lymphoproliferative 57 IgA deficiency 57 acute myocarditis 57 fibrous dysplasia 57 embryonal rhabdomyosarcoma 57 leukoencephalopathy 57 Ewings sarcoma 57 idiopathic thrombocytopenic purpura 57 flaccid paralysis 57 chronic granulomatous disease 56 neurodevelopmental disorder 56 neuroblastoma tumor 56 cardiac fibrosis 56 Dravet syndrome 56 dystrophies 56 Rhabdomyolysis 56 chromosomal anomaly 56 polymorphic ventricular tachycardia 56 arthropathy 56 Muscular dystrophy 56 progressive neurodegenerative disease 56 lysosomal diseases 56 Hirschsprung disease 56 C1 INH deficiency 56 giant cell arteritis 56 nonhereditary 56 Lou Gehrigs disease 56 aneuploidies 56 fibromatosis 56 microdeletion 56 incurable genetic 56 Hirschsprung Disease 56 Severe Combined Immunodeficiency 56 Metastases 56 hydrops 56 progressive neuromuscular 56 inherited neurodegenerative 56 biochemical imbalance 56 Brodmann Area 56 spinal muscular atrophy SMA 56 dissecans 56 chromosomal translocations 56 paraneoplastic 56 diabetes insipidus 56 severe congenital neutropenia 56 ADPKD 56 motor neuron diseases 56 VCFS 56 congenital deficiency 56 Leukemias 56 pulmonary thromboembolism 56 Arnold Chiari Malformation 56 dominantly inherited 56 multisystem disorder 56 Myasthenia gravis 56 cerebri 56 Klinefelter Syndrome 56 degenerative neurological condition 56 monoclonal gammopathy 56 Retinitis pigmentosa 56 Diabetic neuropathy 56 Leber congenital amaurosis LCA 56 spinocerebellar ataxia 56 Henoch purpura 56 medium chain acyl 56 Chronic pancreatitis 56 JAK mutations 56 Chiari malformation 56 MECP2 gene 56 debilitating neurodegenerative disorder 56 achromatopsia 56 chronic obstructive airway 55 susceptibility gene 55 idiopathic epilepsy 55 autosomal recessive 55 autosomal dominant polycystic kidney 55 Sjögren syndrome 55 underlying pathophysiology 55 Von Willebrand disease 55 incurable neurodegenerative disease 55 Hashimoto thyroiditis 55 Sanfilippo Syndrome 55 hypogonadotropic hypogonadism 55 neurofibrillary 55 spastic diplegia 55 Crohns disease 55 Myotonic dystrophy 55 Genetic mutation 55 atrophic 55 LRP5 55 molecular abnormalities 55 channelopathies 55 holoprosencephaly 55 chromosome deletion 55 IRAK1 55 monogenic 55 Chronic lymphocytic leukemia 55 Fibrodysplasia 55 NF2 55 degenerative retinal disease 55 incurable degenerative brain 55 Chronic fatigue 55 nonsense mutation 55 haemochromatosis 55 systemic autoimmune 55 Gorlin syndrome 55 hereditary blindness 55 mitochondrial myopathy 55 Hemochromatosis 55 recessive trait 55 PCNSL 55 McCune Albright 55 Myopathy 55 hereditary degenerative 55 thyroiditis 55 Morquio 55 ectodermal dysplasia 55 Aplastic anemia 55 cri du chat 55 discoid lupus 55 leukodystrophy 55 rhabdomyosarcoma rare cancer 55 Idiopathic 55 Nephrotic Syndrome 55 ataxia telangiectasia 55 HGPS 55 Proteus syndrome 55 gene MECP2 55 cerebellar hypoplasia 55 neurodevelopment disorder 55 immunodeficiencies 55 muscle degeneration 55 entropion 55 Leber Congenital Amaurosis LCA 55 Friedreich ataxia 55 pituitary adenoma 55 hyperinsulinism 55 ANCA associated 55 dysgenesis 55 BRAF V#E 55 osteochondromas 55 dimentia 55 carcinoid tumor 55 cystic kidney 55 cystic fibrosis chronic pancreatitis 55 Eisenmenger syndrome 55 pseudotumor 55 Retinoblastoma 55 Hypophosphatasia 55 neuropathologic 55 Obsessive compulsive disorder 55 positional cloning 55 Stargardt Macular Dystrophy 55 lichen planus 55 susceptibility locus 55 rare chromosomal disorder 55 Syndrome SADS 55 autoimmune hemolytic anemia 55 mosaicism 55 chromosomal defect 55 cardiovascular restenosis cancer 55 recessively inherited 55 choriocarcinoma 55 progressive multifocal PML 55 Glioblastoma Multiforme 55 limb girdle muscular dystrophy 55 fatal neurodegenerative 55 diffuse intrinsic pontine glioma 55 thymic carcinoma 55 Alport Syndrome 55 dermatomyositis 55 MELAS syndrome 55 comorbid anxiety 54 systemic mastocytosis 54 PNET 54 amyloid beta plaques 54 CDH1 54 idiopathic pulmonary 54 Menkes disease 54 arterial calcification 54 de novo mutations 54 metaplasia 54 Dystrophy 54 protein dystrophin 54 transthyretin 54 WAGR syndrome 54 Mitral valve 54 dystrophy 54 myeloproliferative disorder 54 synovial cells 54 LRAT 54 lysosomal enzyme 54 Fragile X Syndrome 54 FTLD 54 hypertrophic 54 Leber hereditary optic neuropathy 54 histiocytosis 54 congenital disorders 54 Frontotemporal Dementia 54 Vitamin B# deficiency 54 immune thrombocytopenic purpura 54 Sudden Arrhythmic Death 54 spastic paraplegia 54 Amyotrophic lateral sclerosis ALS 54 Morquio Syndrome 54 promyelocytic leukemia 54 hemorrhagic colitis 54 Arrhythmogenic 54 ARVD 54 eosinophilic esophagitis 54 cryptogenic 54 Wiskott Aldrich Syndrome 54 hypertrophic cardiomyopathy HCM 54 extramedullary 54 autoimmune encephalitis 54 Lafora 54 Sudden Unexplained Death 54 Pulmonary fibrosis 54 chronic inflammations 54 protein misfolding 54 Chronic Pelvic Pain 54 inherited retinal degeneration 54 neonatal respiratory distress 54 susceptibility genes 54 GPC5 54 progressive degeneration 54 pathophysiologic 54 #q#.# deletion syndrome 54 brain lesions 54 neurodegenerative disorder characterized 54 Medulloblastoma 54 hereditary deafness 54 lysosomal storage diseases 54 Wegener granulomatosis 54 Fatty liver 54 keloid scars 54 Langerhans cell histiocytosis 54 dermopathy 54 Fanconi anemia 54 axonal damage 54 mitochondrial disorders 54 facioscapulohumeral muscular dystrophy 54 undiagnosed celiac disease 54 Guillain Barr 54 autoinflammatory 54 retinitis 54 Tay Sachs Disease 54 Duchenne muscular dystrophy DMD 54 Degenerative 54 aplasia 54 epidermolysis bullosa 54 breast cancer metastasis 54 enzyme deficiency 54 Bardet Biedl syndrome 54 multi infarct dementia 54 congenita 54 Moebius syndrome 54 Diffuse Intrinsic Pontine Glioma 54 renal cysts 54 osteosarcoma bone 54 Myositis 54 pathognomonic 54 osteochondroma 54 Hurler Syndrome 54 APOL1 54 idiopathic PAH 54 Spinal Muscular Atrophy SMA 54 hypermethylated 54 genetic defect 54 Smith Lemli Opitz 54 piriformis syndrome 54 Acidosis 54 hyperparathyroidism 54 immunodeficiency disorder 54 genetic lysosomal storage 54 gastro oesophageal reflux 54 Hereditary angioedema 54 JAK2 enzyme 54 nephrosis 54 osteochondritis dissecans 54 Hypertrophic 54 CHD7 54 cAMP signaling 54 Wilms Tumor 54 osteogenic differentiation 54 progressive degenerative neurological 54 static encephalopathy 54 metabolic abnormality 54 dystrophic 54 DiGeorge Syndrome 54 Crouzon syndrome 54 Usher Syndrome 54 lipoma 54 neuro developmental disorder 54 trophoblastic 54 Oxidative stress 54 Ewing sarcoma bone 54 blastic 54 synaptogenesis 54 genetically inherited 54 chronic myeloid 54 gene APOE4 54 myoclonic epilepsy 54 huntingtin gene 54 demyelinating 54 Raynaud syndrome 54 Eosinophilic 53 amyloid cascade 53 familial ALS 53 Charcot foot 53 degenerative neurological disorder 53 alveolar rhabdomyosarcoma 53 Progeria 53 Genetic variants 53 neurofibromatosis type 53 channelopathy 53 polycystic 53 familial adenomatous polyposis FAP 53 Chiari Malformation 53 decompensated cirrhosis 53 genetic syndromes 53 acute leukemia AML 53 congenital diaphragmatic hernia 53 WDR# 53 FXTAS 53 lupus multiple sclerosis 53 collagen vascular 53 RDEB 53 Periodontitis 53 debilitating complication 53 Cancer cachexia 53 Legg Calvé Perthes disease 53 proliferative disorders 53 β thalassemia 53 MYH9 gene 53 mental retardation epilepsy 53 pancreatic endocrine 53 Venous thromboembolism 53 lymph node enlargement 53 occipital regions 53 Wilms tumors 53 hypothalamic pituitary adrenal axis 53 FSGS 53 Von Hippel Lindau 53 DNA methylation patterns 53 Arteriovenous Malformation 53 MPGN 53 retinitis pigmentosa degenerative 53 Lennox Gastaut Syndrome 53 essential thrombocythemia 53 Ewings Sarcoma 53 physiological abnormalities 53 optic atrophy 53 Magnesium deficiency 53 kidney urologic 53 rheumatoid arthritis lupus 53 epigenetic alterations 53 multiorgan 53 causative genes 53 chronic rheumatic 53 autopsied brains 53 mitochondrial mutations 53 retinal pigment epithelium 53 valvular heart disease 53 ceroid lipofuscinosis NCL 53 neurofibroma 53 recurrent seizures 53 proto oncogene 53 Chronic Myelogenous Leukemia 53 lateral sclerosis ALS 53 granulomatous 53 Synovial Sarcoma 53 Celiac sprue 53 progressive degenerative 53 myalgic encephalomyelitis ME 53 retinitis pigmentosa RP 53 Myelodysplastic syndrome 53 ventricular cardiomyopathy 53 Idiopathic Pulmonary Fibrosis IPF 53 congenital muscular dystrophy 53 inherited mutations 53 Dengue Shock 53 venous thoracic outlet 53 infantile hemangioma 53 progressive retinal degenerative 53 pulmonary metastases 53 metabolic disturbances 53 Avascular necrosis 53 lupus erythematosus 53 Childhood Disorder 53 hereditary hemorrhagic telangiectasia 53 neovascularisation 53 Sjogren Syndrome 53 neuro degenerative disease 53 Kleine Levin 53 nodular melanoma 53 Bruxism 53 Hurthle cell 53 autosomal dominant inheritance 53 anatomical abnormalities 53 Graft Versus Host 53 benign positional vertigo 53 osteogenesis imperfecta OI 53 MEF2A 53 neurogenic bladder 53 multiple sclerosis lupus 53 complement inhibitor eculizumab 53 Wiskott Aldrich syndrome 53 Cowden syndrome 53 abnormal proteins 53 aciduria 53 deafness neurological 53 Clusterin 53 hereditary predisposition 53 missense mutation 53 Diamond Blackfan Anemia 53 dermatosis 53 convulsive seizures 53 skeletal fluorosis 53 ichthyosis vulgaris 53 Spinal cord 53 Male pattern baldness 53 Pervasive Developmental Disorder 53 myoclonus 53 eosinophilic 53 pheochromocytoma 53 urolithiasis 53 clefting 53 Sturge Weber syndrome 53 Systemic lupus erythematosus SLE 53 inappropriate antidiuretic hormone SIADH 53 degenerative neurological disease 53 inflammatory demyelinating 53 arteritis 53 neuro degenerative disorders 53 neuro degenerative 53 mutated protein 53 HLA DRB1 53 genetic loci 53 lacunar 53 hyperplastic 53 histologic findings 53 Basal Cell 53 Angelman syndrome 53 recessive genetic 53 osteoarthritis degenerative 53 rare autosomal recessive 53 Nephrogenic Systemic Fibrosis NSF 53 Irritable bowel syndrome IBS 53 pulmonary hypertension PH 53 blastoma 53 Cellulitis 53 basal cell nevus syndrome 53 papillary carcinoma 53 Meckel Gruber 53 neuritic 53 erythema nodosum 53 Retinopathy 53 retinoblastoma Rb 53 thyroid carcinoma 53 variable immunodeficiency 53 inherited neurodegenerative disorder 53 Krabbe Disease 53 recurrent laryngeal nerve 53 airway hyperresponsiveness 53 mental retardation blindness 53 JMML 53 phthalate syndrome 53 Ehlers Danlos syndrome 53 idiopathic pulmonary arterial hypertension 53 fatal neurological disorder 53 chronic lymphocytic 53 genetic determinants 53 Usher syndrome 53 TTR amyloidosis 53 Pervasive Developmental Disorders 53 connective tissue diseases 53 myotonic dystrophy 53 neurological degeneration 53 Adjuvant therapy 52 Rubinstein Taybi syndrome 52 SSc 52 Joubert syndrome 52 Pompe Disease 52 Osteosarcoma 52 PDGFR 52 familial adenomatous polyposis 52 thymoma 52 chronic idiopathic 52 chromosome #q#.# deletion 52 Tourette Syndrome neurological disorder 52 Iron deficiency anemia 52 CRTAP 52 dysphasia 52 excitotoxicity 52 shortened telomeres 52 Motor neurone disease 52 Klippel Trenaunay Syndrome 52 leaky gut 52 craniofacial defects 52 microsatellite instability 52 fat malabsorption 52 Glioblastoma Multiforme GBM 52 TCF#L# gene 52 Arteriosclerosis 52 collagen VII 52 Sanfilippo syndrome 52 TP# mutation 52 Bullous 52 aniridia 52 cystic fibrosis Duchenne muscular 52 Pancreatic 52 Polycystic Kidney Disease 52 Beta thalassemia 52 Atrial Septal Defect ASD 52 CMV infections 52 Apert syndrome 52 nerve palsy 52 myelodysplasia 52 Alport syndrome 52 chronic cerebro spinal 52 Hurler syndrome 52 beta1 integrin 52 Wilm tumor 52 muscular dystrophies 52 myotonia 52 lymphocytic 52 etiologic 52 dysautonomia 52 pheochromocytomas 52 tau pathology 52 optic neuropathy 52 bulbar 52 cardiac channelopathies 52 retinal blastoma 52 benign paroxysmal positional vertigo 52 Churg Strauss syndrome 52 osteogenic sarcoma 52 Ribavirin causes 52 nephrogenic fibrosing dermopathy 52 Intussusception 52 malignant fibrous histiocytoma 52 Akt pathway 52 retinal dystrophy 52 Cryptococcus neoformans 52 optic nerve hypoplasia 52 autistic enterocolitis 52 carbohydrate intolerance 52 ependymoma 52 Acute myeloid leukemia 52 Alopecia areata 52 Psoriatic arthritis 52 chromosomal instability 52 Crouzon Syndrome 52 Fanconi anemia FA 52 progressively degenerative 52 juvenile myelomonocytic leukemia 52 Amyloid plaques 52 Gastroparesis 52 genetic abnormality 52 chiari malformation 52 neurocysticercosis 52 neurofibromatosis 52 mycosis fungoides 52 spongiform encephalopathies 52 causative mutations 52 Dosa suffers 52 phenotypic expression 52 fatal neuromuscular 52 Wilms tumor 52 cortical dysplasia 52 Acute Myeloid Leukaemia 52 • LI Tourette 52 epidermolysis bullosa EB 52 Takayasu arteritis 52 leukodystrophies 52 Hyperplasia 52 hypertrichosis 52 Canavan Disease 52 tuberous sclerosis complex 52 transfusion syndrome 52 Diamond Blackfan anemia 52 benign polyps 52 thyroid dysfunction 52 dysplasia 52 unprovoked seizures 52 crohn disease 52 BARD1 52 neurodegenerative disease 52 Leukemia lymphoma 52 progranulin gene 52 Epidermolysis bullosa 52 Borderline personality 52 genotoxic stress 52 temporal arteritis 52 incurable degenerative 52 neurologic deficits 52 LRRK2 mutations 52 Raynaud disease 52 Prox1 52 chromosomal deletions 52 degenerative neurological 52 frontotemporal dementia FTD 52 Sporadic CJD 52 hypoplastic 52 encephalitis swelling 52 agenesis 52 cardio myopathy 52 xeroderma pigmentosum 52 MGUS 52 cortical blindness 52 renal fibrosis 52 cutaneous lupus 52 PTLD 52 metastatic gastric 52 NOTCH1 52 subclinical disease 52 choroidal melanoma 52 fibrodysplasia ossificans progressiva FOP 52 acute promyelocytic leukemia 52 Entamoeba histolytica 52 sarcoid 52 pleomorphic 52 prodromal phase 52 neuroblastoma tumors 52 Hemolytic Uremic Syndrome HUS 52 gene rearrangements 52 Charcot Marie Tooth 52 angiosarcoma 52 Cholangiocarcinoma 52 Inflammatory Bowel 52 Mouse Model 52 Enlarged prostate 52 hemolytic anemia 52 muscular dystrophy cystic fibrosis 52 pulmonary metastasis 52 chromosome #q#.# [001] 52 neurodevelopmental disorder characterized 52 Oppositional Defiant Disorder 52 skeletal abnormalities 52 Adult Respiratory Distress 52 untreated celiac disease 52 demyelinating disease 52 Alzheimers disease 52 Dwarfism 52 KRAS oncogene 52 Hypoplastic Left Heart 52 #p# [001] 52 Genetic variation 52 lung fibrosis 52 lipomas 52 meningeal 52 Acute Leukemia 52 constipation predominant irritable bowel 52 MLL2 52 anosognosia 52 underlying molecular mechanisms 52 polyomavirus nephropathy 52 fatal myelination disorder 52 Rhabdomyosarcoma 52 enterocolitis 52 induced cardiomyopathy 52 microdeletions 52 MLH1 52 severe malignant osteopetrosis 52 hereditary nonpolyposis colorectal cancer 52 connective tissue disorders 51 bone marrow mesenchymal stem 51 Eosinophilic Esophagitis 51 granulosa cell 51 splice junctions 51 neurocardiogenic syncope 51 #q#.# [001] 51 Neurodegenerative diseases 51 AAT deficiency 51 Sarcopenia 51 myeloproliferative 51 Zinc deficiency 51 rhabdoid 51 Treacher Collins Syndrome 51 pulmonary hypoplasia 51 childhood disintegrative disorder 51 MAPK pathway 51 Genetic mutations 51 paragangliomas 51 PTEN gene 51 parkin gene 51 Duchene muscular dystrophy 51 polymyositis 51 Bulimia nervosa 51 obstructive coronary 51 immune thrombocytopenic purpura ITP 51 interstitial pneumonitis 51 arthritis gout 51 Neurofibromatosis Type 51 common disabling neurological 51 radiographic findings 51 dystrophin gene 51 Lyme arthritis 51 hyperalgesia 51 Alagille syndrome 51 LRRK2 mutation 51 sCJD 51 heterotopic ossification 51 anaplastic 51 hypotonia 51 skeletal dysplasia 51 mycotic 51 testicular tumors 51 congenital deafness 51 proband 51 precancerous condition 51 neurosyphilis 51 pyloric stenosis 51 suppurative 51 thoracic outlet compression 51 FGFR1 51 LIS1 51 Acute pancreatitis 51 Ischaemic heart 51 susceptibility loci 51 gastrointestinal stromal tumor 51 lymphangioleiomyomatosis LAM 51 Morgellons Disease 51 Malignant glioma 51 lipofuscin 51 amyloid deposits 51 retinal degenerative disease 51 Ulcerative colitis 51 Hemangiomas 51 autonomic dysfunction 51 arrhythmogenic 51 Osteogenesis Imperfecta 51 Genetic susceptibility 51 Treatment Shows Promise 51 myofascial pain syndrome 51 infectious mononucleosis 51 molar pregnancy 51 paresis 51 metastatic malignant 51 progranulin mutations 51 Folic acid deficiency 51 prostatic hyperplasia 51 Myelodysplastic Syndrome 51 degenerative neurological diseases 51 indications Dupuytren 51 supratentorial 51 ectopic expression 51 ADA SCID 51 bullous 51 patella femoral 51 persistent pulmonary hypertension 51 chronicity 51 seizures comas 51 genetic mutation 51 Primary Immunodeficiency 51 lipodystrophy syndrome 51 Atopic dermatitis 51 chromosomal disorder 51 vascular Ehlers Danlos 51 familial hypercholesterolemia 51 Glioma 51 Hypospadias 51 fibroma 51 esophageal reflux 51 Alzeimer 51 biochemical abnormalities 51 Langerhans Cell Histiocytosis 51 transgenic mouse models 51 Parkinson Disease PD 51 neurologic symptoms 51 APOE e4 51 RPE# 51 Idiopathic pulmonary fibrosis IPF 51 filaggrin 51 motor neurones 51 microvascular dysfunction 51 familial clustering 51 gastroesophageal reflux GERD 51 Acute respiratory distress 51 Urticaria 51 alzheimer disease 51 dysplastic 51 interstitial nephritis 51 Coeliac disease 51 IDH mutations 51 medial tibial stress 51 highly heritable 51 autosomal dominant 51 da mage 51 Sclerosing 51 nonsense mutations 51 chromosomal anomalies 51 microglial 51 epididymitis 51 Cystic fibrosis CF 51 Hypertrophic cardiomyopathy 51 tumor suppressor protein 51 Wegener Granulomatosis 51 neurological disorder characterized 51 Benign Paroxysmal Positional Vertigo 51 neovascularization 51 platelet dysfunction 51 Chronic Obstructive Pulmonary 51 Mental retardation 51 undergo apoptosis 51 C1q 51 Antisocial personality 51 dermoid cyst 51 neurocognitive dysfunction 51 1 diabetes T1D 51 C EBP alpha 51 demyelination 51 ductal adenocarcinoma 51 familial hypercholesterolemia genetic 51 GPR# [002] 51 paroxysmal nocturnal hemoglobinuria 51 purpura 51 congenital muscular dystrophies 51 disc degeneration 51 Septicaemia 51 sonographic appearance 51 lupus scleroderma 51 dry scaly skin 51 SMN protein 51 otosclerosis 51 Leber Congenital Amaurosis 51 degenerative disorder 51 necrotizing 51 cervical degenerative disc 51 SOD2 gene 51 Patau syndrome 51 congenital disorder 51 Essential Tremor 51 AA Amyloidosis 51 medulla blastoma 51 Adrenoleukodystrophy 51 optic neuritis 51 Great Imitator 51 lissencephaly 51 hamartoma 51 mammary stem cells 51 Postherpetic neuralgia 51 renal carcinoma 51 Diabetic nephropathy 51 Associated Adipose Redistribution 51 infection progressive multifocal 51 neurons degenerate 51 dystrophin protein 51 nontraumatic 51 malignant pancreatic 51 arthritis lupus 51 Peripheral artery disease 51 epidural abscess 51 Zollinger Ellison Syndrome 51 Sudden Arrhythmia Death 51 chronic inflammatory bowel 51 Huntingtons disease 51 idiopathic scoliosis 51 dysmotility 51 severe aplastic anemia 51 pernicious anemia 51 mucinous 51 Mitochondrial 51 acquired immunodeficiency syndrome 51 predisposing factor 51 diabetes mellitus DM 51 genitourinary tract 51 Dystrophin 51 chromosomal rearrangement 51 Sezary syndrome 51 allograft rejection 51 VHL gene 51 genetic disorder 51 chromosome #q 51 Cerebral malaria 51 esophageal atresia 51 nonalcoholic steatohepatitis 51 degenerative muscular 51 dilated cardiomyopathy 51 Hemorrhagic 51 carcinoid 51 SHANK3 51 arrhythmogenic right 51 Benign prostatic hyperplasia 51 Dental fluorosis 51 non polyposis colorectal 51 lateral sclerosis 51 Parkinsons Disease 51 Trigeminal neuralgia 51 Stargardt Macular Dystrophy SMD 51 Major depressive disorder 51 obliterative bronchiolitis 51 Immune Thrombocytopenic Purpura 51 Joubert syndromes 51 PB1 F2 51 Pemphigus 51 insoluble plaques 51 Chronic inflammation 51 Smad7 51 angioma 51 Neuropathic 51 motor neuropathy 51 allogeneic bone marrow 51 prenatally diagnosed 51 primitive neuroectodermal tumor 51 intracranial hypertension 51 astrocytic 51 epigenetic modification 51 debilitating neurological disease