Related by context. All words. (Click for frequent words.) 69 retinitis pigmentosa RP 65 Leber congenital amaurosis 65 Stargardt Macular Dystrophy 65 glaucoma diabetic retinopathy 64 prematurity ROP 63 retinitis pigmentosa degenerative 63 Leber congenital amaurosis LCA 63 inherited retinal 62 irreversible blindness 62 neovascular 62 Leber Congenital Amaurosis LCA 62 Stargardt Macular Dystrophy SMD 62 presumed ocular histoplasmosis 62 corneal scarring 62 optic atrophy 62 Leber hereditary optic neuropathy 61 progressive retinal degenerative 61 dominantly inherited 61 macular disease 61 choroidal neovascularization CNV 61 aniridia 61 congenital blindness 61 proliferative retinopathy 61 choroidal neovascularisation 61 Retinitis Pigmentosa RP 61 ocular angiogenesis 60 hereditary spastic paraplegia 60 diabetic retinopathy DR 60 hereditary degenerative 60 progressive neurodegenerative 60 Stargardt macular dystrophy 60 retinitis 60 retinal dysfunction 60 Cockayne syndrome 60 autosomal dominant polycystic kidney 60 retinitis pigmentosa hereditary 60 retinal pigment epithelium 60 progressive neurodegenerative disorder 60 wet macular degeneration 60 NPHP 60 LHON 60 Retinitis pigmentosa 60 predominantly classic subfoveal 60 achromatopsia 60 systemic amyloidosis 60 inherited neurological disorder 59 inherited retinal degeneration 59 retinal dystrophy 59 congenital glaucoma 59 pathologic myopia 59 Lupus nephritis 59 Stargardt Disease 59 hereditary retinal 59 Von Willebrand disease 59 pigmentosa 59 cortical dysplasia 59 retinitis pigmentosa 59 choroidal vasculopathy 59 choroidal neovascularization 59 congenital achromatopsia 59 exudative 59 inherited neurodegenerative 59 ischemic optic neuropathy 59 dyskeratosis congenita 59 incurable genetic 59 Macular edema 59 Alport syndrome 59 dystrophies 59 optic neuritis 59 autosomal dominant disorder 58 dilated cardiomyopathy DCM 58 monogenic 58 Usher Syndrome 58 glaucoma cataract 58 autosomal recessive genetic 58 Ehlers Danlos syndrome 58 Wet AMD 58 autosomal recessive disease 58 cystic fibrosis chronic pancreatitis 58 genetic lysosomal storage 58 brain malformation 58 branch retinal vein 58 hereditary blindness 58 neuropsychiatric disorder 58 septo optic dysplasia 58 neurodegenerative disorder 58 Parkinson degenerative 58 Neurofibromatosis type 58 MELAS 58 Retinopathy 58 RPE# 58 degenerative neurological disorder 58 chronic obstructive airway 58 Myotonic dystrophy 58 Huntingtons disease 58 Macular degeneration 58 macular degeneration glaucoma 58 neurodegenerative disorder characterized 58 muscular dystrophy cystic fibrosis 58 multiorgan 58 optic nerve hypoplasia 58 TTR amyloidosis 57 holoprosencephaly 57 common neurovascular complication 57 immunodeficiencies 57 optic neuropathy 57 Eisenmenger syndrome 57 leptin deficiency 57 diffuse intrinsic pontine glioma 57 Diabetic retinopathy 57 fatal neurodegenerative disorder 57 syringomyelia 57 Lafora disease 57 Urinary tract 57 retinal degeneration 57 retinal degenerations 57 kidney urologic 57 debilitating neurodegenerative disorder 57 Maroteaux Lamy Syndrome 57 neovascular wet age 57 recessive dystrophic epidermolysis bullosa 57 retinal pigment epithelial 57 keratoconjunctivitis sicca 57 enzyme deficiency 57 degenerative disorder 57 familial adenomatous polyposis FAP 57 recessive trait 57 geographic atrophy 57 hereditary deafness 57 rod photoreceptors 57 SSc 57 Beta thalassemia 57 dry scaly skin 57 Genetic mutation 57 ocular albinism 57 congenital cataract 57 multi infarct dementia 57 multifactorial disease 57 autosomal recessive disorder 57 retina macula 57 Osteogenesis imperfecta 57 recessive genetic 57 progressive degeneration 57 diabetic retinopathy glaucoma 57 platelet dysfunction 56 atypical hemolytic uremic syndrome 56 immunodeficiency disorder 56 incurable neurodegenerative disease 56 Hutchinson Gilford progeria 56 Fuchs dystrophy 56 primary ciliary dyskinesia 56 glaucoma cataracts 56 glaucoma macular degeneration 56 Ribavirin causes 56 thyroid hormone deficiency 56 multisystem disorder 56 Lesch Nyhan syndrome 56 pseudotumor cerebri 56 autosomal dominant 56 occlusion CRVO 56 Li Fraumeni syndrome 56 gene MECP2 56 autoimmune encephalitis 56 prematurity Stargardt disease 56 valvular heart disease 56 macular degeneration diabetic retinopathy 56 central retinal vein 56 macular edema secondary 56 retinal 56 Hutchinson Gilford Progeria Syndrome 56 Marfan syndrome connective tissue 56 Retinal vein occlusion 56 Hypophosphatasia 56 Proteus syndrome 56 chromosome #q#.# deletion 56 dysgenesis 56 Pulmonary hypertension 56 Tuberous sclerosis 56 neurological disorder affecting 56 Uveal melanoma 56 truncus arteriosus 56 cataracts glaucoma 56 neural degenerative diseases 56 Hurler syndrome 56 neovascularisation 56 paroxysmal nocturnal hemoglobinuria 56 cardiac fibrosis 56 abdominal abscesses 56 Bullous 56 Myelodysplastic syndrome 56 fatal neurodegenerative 56 cystic kidney 56 Leber Congenital Amaurosis 56 abnormal angiogenesis 56 Zinc deficiency 56 sporadic Creutzfeldt Jakob 55 retinal vein occlusion 55 severe malignant osteopetrosis 55 purpura 55 Wet macular degeneration 55 multisystem disease 55 nonarteritic anterior ischemic optic 55 renal kidney 55 neurological manifestations 55 macular 55 interstitial nephritis 55 AAT deficiency 55 Retinitis Pigmentosa 55 retinal degenerative disease 55 Arrhythmogenic Right Ventricular Cardiomyopathy 55 retinoblastoma rare 55 NF2 55 neuronal dysfunction 55 congenital cataracts 55 anterior ischemic optic neuropathy 55 Usher syndrome 55 microangiopathy 55 neovascular form 55 Medulloblastoma 55 skeletal dysplasia 55 xeroderma pigmentosum 55 iritis 55 fibrodysplasia ossificans progressiva 55 Fanconi anemia FA 55 incurable neurological disorder 55 neovascularization 55 retinal vascular 55 lysosomal storage disease 55 Crouzon syndrome 55 interstitial pneumonitis 55 Idiopathic pulmonary fibrosis IPF 55 autosomal recessive 55 neurological disorders orphan 55 sarcoid 55 cutaneous lupus 55 incurable degenerative 55 evaporative dry 55 metachromatic leukodystrophy 55 Cystic fibrosis CF 55 Gorlin syndrome 55 Ischaemic heart 55 lateral sclerosis ALS 55 deCODE Glaucoma TM 55 LRAT 55 leukoencephalopathy 55 corneal swelling 55 progressively degenerative 55 phthalate syndrome 55 chromosome abnormality 55 recessively inherited 55 MELAS syndrome 55 paralysis blindness 55 retinal pigment epithelium RPE 55 CRVO 55 Retinoblastoma 54 ceroid lipofuscinosis NCL 54 alpha1 antitrypsin deficiency 54 Inflammatory Bowel 54 chronic granulomatous disease 54 Henoch purpura 54 myotonia 54 AMD diabetic retinopathy 54 uterine tumors 54 subretinal 54 mastocytosis 54 optica 54 Chronic myeloid leukemia CML 54 imperfecta 54 amino acid cystine accumulates 54 incurable neurological 54 aplasia 54 Myasthenia gravis 54 corneal edema 54 Bardet Biedl syndrome 54 Barrett esophagus precancerous 54 bacterial endocarditis 54 photokeratitis 54 autoinflammatory diseases 54 iSONEP ™ 54 retinal blindness 54 inherited neurodegenerative disorder 54 pathological hallmark 54 Severe Combined Immunodeficiency 54 Duchene muscular dystrophy 54 bullous 54 corneal inflammation 54 ADPKD 54 blood clotting disorder 54 cystic fibrosis muscular dystrophy 54 lysosomal storage diseases 54 cysticercosis 54 Pompe Disease 54 aMCI precursor 54 degenerative neurological condition 54 lissencephaly 54 diabetic retinopathy macular degeneration 54 proliferative diabetic retinopathy 54 macular degeneration 54 hypertrichosis 54 mucus glands 54 degenerative neurological disease 54 Peptic ulcer 54 membranous nephritis 54 osteopetrosis 54 ANCA associated 54 Hereditary angioedema HAE 54 neurocysticercosis 54 familial adenomatous polyposis 54 maculopathy 54 chronic inflammatory bowel 54 neurogenic bladder 54 huntingtin gene 54 Pancreatic insufficiency 54 Sandhoff disease 54 hypometabolism 54 static encephalopathy 54 Pulmonary fibrosis 54 Stargardt disease 54 Diffuse Intrinsic Pontine Glioma 54 Spinal muscular atrophy 54 PLX STROKE targeting 54 treat musculoskeletal metabolic 54 Macular degeneration affects 54 hydrops 54 Leber Hereditary Optic Neuropathy 54 diabetes insipidus 54 epidermolysis bullosa 54 Optic nerve 54 retinal pigment epithelial cells 54 severe obstructive pulmonary 54 Down syndrome chromosomal disorder 54 implantable telescope 54 Wolf Hirschhorn 54 degenerative retinal diseases 54 Systemic lupus erythematosus SLE 54 retinal pigment 54 RPE# gene 54 cataracts clouding 54 retinal diseases 54 Diamond Blackfan Anemia 54 Dysplasia 54 Joubert syndrome 54 velo cardio facial 54 disorder FASD 54 hypercholesterolemia liver 54 lymphatic vasculature 54 Becker muscular dystrophy 54 hemorrhagic colitis 54 autoimmune uveitis 54 neuro developmental disorder 54 corneal opacity 54 neurofibromas 54 Diabetic nephropathy 54 Sjogren Syndrome 54 Degenerative diseases 54 congenital muscular dystrophy 54 Diabetic macular edema 53 Aortic stenosis 53 melanin pigment 53 plexiform 53 Adenoviral 53 retinal ischemia 53 Acute myeloid leukemia 53 Sanfilippo Syndrome 53 untreatable blindness 53 chronic autoimmune disorder 53 retinal degenerative diseases 53 nephritis 53 Chronic sinusitis 53 Chiari malformation 53 myelopathy 53 cone photoreceptors 53 capillary leakage 53 AAT Deficiency 53 Kufs disease 53 myotonic muscular dystrophy 53 Myocarditis 53 Urticaria 53 renal failure interstitial lung 53 CMV retinitis 53 waterborne organism 53 limb malformations 53 Alport Syndrome 53 retinal vein occlusion RVO 53 degenerative nerve 53 encephalitis swelling 53 Morquio Syndrome 53 nonalcoholic cirrhosis 53 neuronal ceroid lipofuscinosis 53 erythema nodosum 53 infantile hemangioma 53 tuberous sclerosis complex 53 Atopic dermatitis 53 Iron deficiency anemia 53 hereditary predisposition 53 neuro degenerative 53 motor neuron degeneration 53 hypophosphatasia 53 congenital hypothyroidism 53 homozygous FH 53 Fragile X gene 53 congenital deficiency 53 chiari malformation 53 chronic rheumatic 53 Morquio syndrome 53 lens opacities 53 iSONEP TM 53 Amblyopia 53 hereditary hemorrhagic telangiectasia 53 polydactylism 53 Malignant glioma 53 progressive degenerative neurological 53 Crouzon Syndrome 53 jaundice yellowing 53 Pelvic inflammatory 53 NAGS deficiency 53 congenital disorders 53 6 phosphate dehydrogenase 53 treating psychiatric disorders 53 neuroblastoma tumor 53 Nonalcoholic fatty liver 53 nerve degeneration 53 paraganglioma 53 strabismus crossed 53 thalassemia sickle cell 53 Diabetic Retinopathy DR 53 headaches nausea vomiting 53 interstitial fibrosis 53 neuritic 53 retinal dystrophies 53 lymphoma myeloma 53 Niemann Pick disease 53 Seborrheic dermatitis 53 epilepsy Parkinson disease 53 inflammatory demyelinating 53 Devic disease 53 deafness neurological 53 fronto temporal dementia 53 fibrosarcoma 53 immuno deficiency 53 Amyotrophic lateral sclerosis 53 genetically inherited 53 alpha1 antitrypsin AAT deficiency 53 leukodystrophy 53 discoid lupus 53 dermopathy 53 genetic neuromuscular disorder 53 obstructive pulmonary disease 53 NASH Huntington 53 epidermolysis bullosa EB 53 myelogenous leukemia 53 Obstructive sleep apnea OSA 53 DiGeorge syndrome 53 cardiovascular restenosis cancer 53 myoclonus 53 lichen planus 53 diabetic macular edema 53 fibrodysplasia ossificans progressiva FOP 53 cardiac hypertrophy 53 cystic fibrosis sickle cell 53 renal tubules 53 autoinflammatory 53 thyroid deficiency 53 pulmonary hypertension PH 53 gastrointestinal dysfunction 53 toxocariasis 53 Critical limb ischemia 53 blastoma 53 degenerative neuromuscular disease 53 uveitis 53 ocular inflammatory 53 neurofibroma 53 choroidal melanoma 53 disease epidermolysis bullosa 53 atrophic 53 cortical blindness 53 Krabbe Leukodystrophy 53 endocrine disorder 53 anosognosia 53 vitreous floaters 53 nephropathic cystinosis 53 Bacterial conjunctivitis 53 rare autosomal recessive 53 dystrophy 53 limbal stem cell 53 Factor XIII 53 interstitial cystitis 53 Sjögren syndrome 53 frontotemporal 53 polymorphic ventricular tachycardia 53 idiopathic PAH 53 C1 INH deficiency 53 Enlarged prostate 53 fibrosing 52 Hemangiomas 52 Ischemic 52 optic neuropathy NAION 52 colic diarrhea 52 Fibrous Dysplasia 52 wet exudative 52 severe dehydrating diarrhea 52 WAGR syndrome 52 Muscular dystrophy 52 malignant pancreatic 52 progressive degenerative 52 glomerulonephritis 52 pituitary adenoma 52 neurosensory 52 arthropathy 52 severe congenital neutropenia 52 congenital disorder 52 obliterative bronchiolitis 52 Diabetic neuropathy 52 pathological hallmarks 52 spleen enlargement 52 thyroiditis 52 adenosine deaminase 52 inappropriate antidiuretic hormone SIADH 52 hereditary emphysema 52 facial palsy 52 Neovascular 52 commercializes innovative biopharmaceuticals 52 lupus multiple sclerosis 52 Crigler Najjar syndrome 52 Degeneration AMD 52 tricuspid atresia 52 chronic lymphocytic 52 neuro degenerative disease 52 retinal edema 52 neonatal respiratory distress 52 idiopathic pulmonary 52 parathyroid carcinoma 52 cerebral ischemia 52 vasculopathy 52 arteriovenous malformations 52 leukoencephalopathy PML 52 myasthenia gravis neuromuscular 52 Atopic eczema 52 biliary atresia rare 52 muscular spasticity 52 diabetic macular edema DME 52 craniofacial deformities 52 von Hippel Lindau 52 occipital regions 52 retinal detachment 52 axonal damage 52 elevated IOP 52 cerebral palsy epilepsy 52 Waldenstrom macroglobulinemia 52 Arnold Chiari Malformation 52 debilitating neurodegenerative 52 corneal epithelial 52 muscular degeneration 52 muscle degeneration 52 leukemias lymphomas 52 disseminated intravascular coagulation 52 diabetic retinopathy 52 Amyotrophic lateral sclerosis ALS 52 Benign Paroxysmal Positional Vertigo 52 entropion 52 leukemia lymphomas 52 polycystic 52 detached retinas 52 neurofibromatosis type 52 autoimmune thyroiditis 52 ophthalmologic disorders 52 corneal ulcers 52 Macular Degeneration 52 variable immunodeficiency 52 lysosomal storage disorder 52 cervical degenerative disc 52 Endometrial cancer 52 retinal tissue 52 induced cardiomyopathy 52 histiocytosis 52 defective cilia 52 retinopathy 52 transthyretin amyloidosis 52 bulbar 52 Mouse Model 52 Ulcerative colitis 52 skeletal fluorosis 52 autosomal dominant inheritance 52 rheumatoid arthritis inflammatory bowel 52 tics involuntary 52 blindness 52 capillary leak 52 atresia 52 choroidal 52 behavioral abnormalities 52 Folic acid deficiency 52 hypercalcaemia 52 Moraxella bovis 52 vitreous hemorrhage 52 1 diabetes T1D 52 Associated Adipose Redistribution 52 polymyalgia rheumatica 52 Menkes disease 52 chronic immune thrombocytopenic 52 Hemiplegia 52 Dilated cardiomyopathy 52 Wernicke Korsakoff syndrome 52 degenerative muscular 52 chronic progressive neurodegenerative 52 invasive fungal 52 transfusion syndrome 52 Benign prostatic hyperplasia 52 Meckel Gruber 52 complement inhibitor eculizumab 52 Malignant mesothelioma 52 Obsessive compulsive disorder 52 papilledema 52 rare chromosomal disorder 52 cornea clouding vision 52 gastro esophageal reflux 52 Syndrome LEMS 52 Magnesium deficiency 52 lymphocytic leukemia 52 spastic diplegia 52 CFTR gene 52 Cerebral malaria 52 cardiac insufficiency 52 photoreceptor cells 52 periventricular 52 acne eczema 52 cytomegalovirus infection 52 Relapsing remitting MS 52 ataxias 52 cause cardiac channelopathies 52 diseases chronic granulomatous 52 necrotizing enterocolitis NEC 52 cerebral vascular disease 52 Lennox Gastaut syndrome 52 chorea associated 52 Degenerative disc disease 52 related maculopathy 52 fungoides 52 LSCD 52 Systemic lupus 52 hyperplastic 52 Frontotemporal dementia 52 ductal adenocarcinoma 52 nonvascular 52 dysmotility 52 cerebellar ataxia 52 nonischemic 52 cystic fibrosis Duchenne muscular 52 pyloric stenosis 52 skeletal deformities 52 retinal bleeding 52 neurological degeneration 52 JMML 52 Hurler Syndrome 52 severely impairs 52 Duchenne muscular dystrophy DMD 52 progeria rare 52 neovascular AMD 52 neurological dysfunction 52 debilitating neurological disease 52 lumbar degenerative 52 Polycystic kidney disease 52 congenital insensitivity 52 gastrointestinal GI perforation 52 CP CPPS 52 Raynaud disease 52 pancytopenia 52 multi factorial disease 52 Antisocial personality 52 severe ocular allergies 52 Nephrogenic Systemic Fibrosis NSF 52 #beta HSD1 52 psoriasis Crohn disease 52 benign paroxysmal positional vertigo 52 mental retardation cerebral palsy 52 Angelman syndrome 52 Idiopathic pulmonary fibrosis 52 blastic 52 fat malabsorption 52 arterial calcification 52 lung fibrosis 52 anterior uveitis 52 Maroteaux Lamy syndrome 52 impaired cognition 52 retinoblastoma cancerous tumor 52 coagulopathy 52 Hemorrhagic stroke 52 spinocerebellar ataxia 52 bilateral retinoblastoma 52 bacterium Mycobacterium tuberculosis 52 convulsions tremors 52 myelodysplasia 52 regenerating tissues 52 neurocognitive dysfunction 52 bladder tumors 52 fatal neuromuscular disorder 52 esophageal atresia 52 plasma kallikrein 52 Shwachman Diamond Syndrome 52 idiopathic epilepsy 52 familial ALS 52 nephrosis 52 Neovascular Age Related Macular 52 Cholangiocarcinoma 52 precancerous condition 52 Cryptococcus neoformans 52 retinal pigment epithelial RPE 52 MPGN 52 insulin secreting beta 51 persistent pulmonary hypertension 51 Systemic lupus erythematosus 51 Idiopathic Pulmonary Fibrosis IPF 51 CHARGE syndrome 51 photoreceptor cell 51 suppurative 51 Klippel Trenaunay Syndrome 51 Peripheral artery disease 51 quadriplegic cerebral palsy 51 Hereditary angioedema 51 Proteus Syndrome 51 artery stenosis 51 abnormal genital 51 avascular 51 leiomyomas 51 Chronic pancreatitis 51 cataracts 51 opsoclonus myoclonus syndrome 51 retinoblastoma 51 hemophagocytic lymphohistiocytosis 51 Heavy menstrual bleeding 51 exudative AMD 51 primary pulmonary hypertension 51 protein misfolding diseases 51 Acne vulgaris 51 polymyalgia 51 neovascular age 51 congenita 51 hypereosinophilic syndrome 51 Churg Strauss syndrome 51 Wegener granulomatosis 51 perinatal asphyxia 51 Parkinson disease degenerative 51 systemic autoimmune 51 Dental fluorosis 51 vWD 51 myoclonic epilepsy 51 granulomatous 51 nephropathy kidney 51 cardiomyopathy weakening 51 amblyopia lazy eye 51 included exfoliative dermatitis 51 Prematurity ROP 51 Tourette Syndrome TS 51 angioma 51 neurodevelopmental disorder 51 mitochondrial myopathy 51 Alzheimer disease vascular dementia 51 chromosomal defect 51 defects refraction cataracts 51 dimentia 51 Korsakoff syndrome 51 polycystic kidneys 51 mediated amyloidosis ATTR hypercholesterolemia 51 Pervasive Developmental Disorders 51 neonatal jaundice 51 osteogenesis imperfecta OI 51 disorder thalassemia 51 1 proteinase inhibitor 51 Clinically significant 51 thrombocytopenia neutropenia 51 extraocular 51 homozygous familial hypercholesterolemia 51 Gastro intestinal 51 Neurofibromatosis Type 51 Leukodystrophy 51 esophageal reflux 51 uvea 51 Acute Bacterial Sinusitis ABS 51 abnormal p# 51 Thyroid hormone 51 corneal infections 51 PAOD 51 Hormonal imbalance 51 dilated cardiomyopathy 51 osteochondrosis 51 Retinal detachment 51 Esophagitis 51 urolithiasis 51 progressive neuromuscular 51 BH4 deficiency 51 Sclerosing 51 Psoriatic arthritis 51 Postherpetic neuralgia PHN 51 dissecans 51 meningeal 51 Coeliac disease 51 degenerative neurological diseases 51 kidney insufficiency 51 biliary tract 51 craniofacial abnormalities 51 intravitreal injections 51 keratoconus 51 biliary obstruction 51 Sezary syndrome 51 necrotising 51 Moyamoya 51 filaggrin 51 insoluble plaques 51 Pulmonary arterial hypertension 51 Dr. Isaac Lipshitz 51 hypokalemia hypomagnesemia 51 allergic airway 51 Gastroparesis 51 hematologic disorders 51 Epidermolysis bullosa 51 geographic atrophy GA 51 Angelman 51 IRS1 51 paraneoplastic 51 hemorrhagic pancreatitis 51 multiforme 51 abnormal uterine bleeding 51 levodopa induced 51 demyelinating 51 chronic myeloid 51 ichthyosis vulgaris 51 macular edema 51 hereditary disorder 51 treat neovascular wet 51 generalized epilepsy 51 Pervasive Developmental Disorder 51 channelopathies 51 respiratory gastrointestinal 51 Hypertrophic 51 Holoprosencephaly 51 nonsense mutations 51 Arrhythmogenic 51 fungus Fusarium 51 acute myeloid 51 Hutchinson Gilford Progeria 51 patent ductus arteriosus 51 immunodeficiency diseases 51 neurologic disorder 51 Relapsing remitting 51 Mitral regurgitation 51 juvenile myoclonic epilepsy 51 Diamond Blackfan anemia 51 neurodevelopment disorder 51 myopathies 51 incurable degenerative brain 51 ADAMTS# 51 chronic renal insufficiency 51 Parkinson disease multiple sclerosis 51 epiretinal 51 thoracic aortic aneurysm 51 chronic venous insufficiency 51 bone deformities 51 irreversible neurological disorder 51 infantile onset 51 oculomotor 51 Brugada Syndrome 51 computed tomography angiography 51 Alzheimers disease 51 cheilitis 51 chromosomal anomaly 51 urinary blockage 51 sensory disturbances 51 Foetal alcohol 51 neurogenetic 51 thymic carcinoma 51 retinal transplantation 51 obstructive sleep 51 hyperinsulinism 51 vanA gene 51 immunodeficiency 51 idiopathic thrombocytopenic purpura 51 bronchopulmonary dysplasia 51 multiple sclerosis amyotrophic lateral 51 Glioblastoma Multiforme GBM 51 Hashimoto thyroiditis 51 urothelial cancer 51 idiopathic thrombocytopenic purpura ITP 50 myotonic dystrophy 50 uremic 50 Peripheral arterial disease 50 Childhood Disorder 50 untreated obstructive sleep 50 vascular occlusive diseases 50 Severe Primary IGFD 50 transgenic mouse models 50 neovascular diseases 50 microvessel 50 robs sufferers 50 often reversible neuropsychiatric 50 Occlusive Disease 50 WDR# 50 brain lesions 50 mycobacterial infection 50 medium chain acyl 50 Borderline personality 50 Age Related Macular 50 Trigeminal neuralgia 50 neuron degeneration 50 hemolytic anemia 50 hypoplastic 50 acetonide FA 50 embolic stroke 50 glare halos 50 Hyperthyroidism 50 Pericarditis 50 collagen vascular 50 ventricular dilation 50 Parkinsons disease 50 survival motor neuron 50 myopia nearsightedness 50 Arteriovenous Malformation 50 rheumatoid arthritis lupus 50 Raynaud syndrome 50 motor neuron diseases 50 Autoimmune hepatitis 50 autoimmune hemolytic anemia 50 diffuse axonal injury 50 roseola 50 engineered RAP peptides 50 hyperthyroidism 50 Keratitis 50 keratitis 50 chronic thromboembolic pulmonary 50 bicuspid valve 50 PKU genetic 50 hyperopia farsightedness 50 Irritable bowel syndrome IBS 50 myopia hyperopia 50 epilepsy multiple sclerosis 50 liver cancers TTR 50 Lou Gehrigs disease 50 Ankylosing spondylitis 50 Polycythemia vera 50 Atrial Septal Defect ASD 50 dysphasia 50 polydipsia 50 homocystinuria 50 infantile hemangiomas 50 pulmonary thromboembolism 50 Degenerative Disc Disease 50 pigmented layer 50 runny nose irritated 50 degenerative neurological 50 Pelizaeus Merzbacher disease 50 Anaplasmosis 50 Melasma 50 Loeys Dietz syndrome 50 Myelodysplastic Syndrome 50 uveal tract 50 multigenic 50 corneal diseases 50 corneal transplantation 50 Acute pancreatitis 50 Postherpetic neuralgia 50 neurobehavioral disorders 50 Congenital Muscular Dystrophy 50 uremia 50 pseudophakic 50 hyperparathyroidism 50 subependymal giant cell 50 fatal myelination disorder 50 laser photocoagulation 50 nonsense mutation 50 Primary immunodeficiency 50 cholestasis 50 meningitis inflammation 50 Tourette Syndrome neurological disorder 50 cyanosis 50 alzheimer disease 50 hippocampal function 50 phakic 50 anatomical abnormalities 50 Friedreich 50 common disabling neurological 50 Bronchiectasis 50 acne psoriasis 50 neurofibromatosis 50 Celiac sprue 50 infection progressive multifocal 50 Fatty liver 50 choroid 50 myelin sheath fatty 50 renal fibrosis 50 juvenile myelomonocytic leukemia 50 retina 50 fibroma 50 congenital 50 non arteritic anterior ischemic 50 gastro oesophageal reflux 50 hydrocephaly 50 Primary IGFD 50 galactosemia 50 genus Plasmodium 50 Ventricular Septal Defect 50 biliary atresia