Related by context. All words. (Click for frequent words.) 77 degenerative neurological disorder 75 neurodegenerative disorder 75 progressive neurological disorder 74 degenerative neurological disease 74 progressive degenerative 73 progressive neurodegenerative disorder 72 incurable neurological disorder 71 genetic disorder 71 neurological disorder 71 Usher Syndrome 71 Krabbe Leukodystrophy 70 fatal neurodegenerative 70 brain malformation 70 degenerative neuromuscular disease 70 degenerative disease 70 inherited neurological disorder 69 Parkinson disease degenerative 69 hereditary disorder 69 fatal neurodegenerative disorder 69 progressive neurodegenerative disease 69 Angelman syndrome 68 inherited neurodegenerative disorder 68 myotonic dystrophy 68 fatal neuromuscular disorder 68 cerebellar ataxia 68 debilitating neurological disorder 68 motor neuron disease 68 Leber Congenital Amaurosis LCA 68 Retinitis pigmentosa 68 Joubert syndrome 68 mitochondrial myopathy 67 mitochondrial disease 67 Leber congenital amaurosis LCA 67 hereditary degenerative 67 progressive neurodegenerative 67 progressive degeneration 67 Multiple sclerosis MS 67 degenerative nerve disease 67 Parkinson degenerative 67 CHARGE syndrome 67 enzyme deficiency 66 neurodegenerative disease 66 Leber congenital amaurosis 66 Motor neurone disease 66 neurological disorder affecting 66 Krabbe Disease 66 inherited retinal degeneration 66 epidermolysis bullosa EB 66 Essential tremor 66 Pulmonary fibrosis 66 chronic autoimmune disorder 66 Muscular dystrophy 66 autoimmune disease 66 Pompe Disease 66 Myasthenia gravis 66 septo optic dysplasia 66 degenerative nerve disorder 66 Proteus syndrome 66 embryonal rhabdomyosarcoma 66 arthrogryposis 66 Krabbe disease 66 Wiskott Aldrich Syndrome 65 blood clotting disorder 65 degenerative neurological condition 65 congenital disorder 65 Myotonic dystrophy 65 Retinoblastoma 65 debilitating autoimmune 65 Spinal muscular atrophy 65 chromosome abnormality 65 neuro degenerative disorder 65 incurable genetic 65 retinitis pigmentosa RP 65 ataxia telangiectasia 65 Fanconi anemia 65 neurofibromatosis 65 leukodystrophy 65 Krabbe leukodystrophy 65 dyskeratosis congenita 65 Amyotrophic lateral sclerosis 65 incurable neurodegenerative disease 65 Polycystic kidney disease 65 Medulloblastoma 65 Sanfilippo Syndrome 65 Parkinson disease neurological disorder 65 inflammatory demyelinating 65 optic nerve hypoplasia 65 multiple sclerosis degenerative 65 Amyotrophic lateral sclerosis ALS 65 chromosomal defect 65 Hutchinson Gilford Progeria Syndrome 65 spastic paraplegia 64 retinitis pigmentosa degenerative 64 spinocerebellar ataxia 64 Brugada Syndrome 64 Usher syndrome 64 inherited neurodegenerative 64 ectodermal dysplasia 64 Pulmonary hypertension 64 Hurler Syndrome 64 Ehlers Danlos syndrome 64 immunodeficiency disorder 64 Coeliac disease 64 progressive neuromuscular 64 Maroteaux Lamy Syndrome 64 Friedreich ataxia 64 Maroteaux Lamy syndrome 64 neuro degenerative disease 64 dominantly inherited 64 spinal muscular atrophy SMA 64 Rhabdomyosarcoma 64 neurodegenerative disorder characterized 64 myalgic encephalomyelitis ME 64 Cystic fibrosis CF 64 Cerebral palsy 64 blastoma 64 chronic neurological disorder 64 neuromuscular disorder 64 rare neurological disorder 64 degenerative 64 degenerative nerve 64 Angelman Syndrome 64 epidermolysis bullosa 64 Hutchinson Gilford progeria 64 Diabetic neuropathy 64 Niemann Pick disease 64 spastic diplegia 64 hereditary spastic paraplegia 63 debilitating neurological disease 63 genetic defect 63 juvenile myelomonocytic leukemia 63 Neurofibromatosis type 63 autoimmune disorder 63 chromosomal disorder 63 Stargardt disease 63 Hurler syndrome 63 Pompe disease rare 63 autosomal dominant polycystic kidney 63 neuromuscular disease 63 tuberous sclerosis complex 63 Proteus Syndrome 63 holoprosencephaly 63 Macular degeneration 63 Aicardi syndrome 63 fatal neuromuscular 63 chronic degenerative 63 Parkinsons disease 63 Wilm Tumor 63 ADPKD 63 static encephalopathy 63 Retinitis Pigmentosa RP 63 Parkinsons Disease 63 Lou Gherig Disease 63 polycystic kidney disease 63 Arnold Chiari Malformation 63 Hypophosphatasia 63 Cystic fibrosis 63 neuro muscular disorder 63 Ewing sarcoma bone 63 incurable neurological 63 metachromatic leukodystrophy 63 Aplastic anemia 63 juvenile dermatomyositis 63 Becker muscular dystrophy 62 Polycystic Kidney Disease 62 Diffuse Intrinsic Pontine Glioma 62 spastic cerebral palsy 62 degenerative muscular 62 quadriplegic cerebral palsy 62 Von Willebrand disease 62 Rubinstein Taybi syndrome 62 lateral sclerosis 62 NF2 62 rare chromosomal disorder 62 neuro developmental disorder 62 discoid lupus 62 Joubert Syndrome 62 neuropsychiatric disorder 62 Hereditary angioedema HAE 62 Dravet syndrome 62 Crouzon Syndrome 62 chronic granulomatous disease 62 Lafora disease 62 supranuclear palsy 62 achondroplasia 62 dilated cardiomyopathy 62 metabolic disorder 62 hemophagocytic lymphohistiocytosis 62 lateral sclerosis ALS 62 reflex sympathetic dystrophy 62 Crohn disease chronic 62 congenital muscular dystrophy 62 Stargardt Macular Dystrophy 62 transverse myelitis 62 DiGeorge syndrome 62 achromatopsia 62 disabling neurological 62 retinal dysfunction 62 retinitis pigmentosa 62 cerebral palsy neurological disorder 62 Canavan Disease 62 Marfan Syndrome 62 Osteosarcoma 62 autonomic neuropathy 62 fatal neurological disorder 62 Jakob Disease 62 hereditary blindness 62 Lou Gherig disease 62 rhabdomyosarcoma rare 62 Idiopathic pulmonary fibrosis IPF 62 neurological dysfunction 62 incurable degenerative 62 Multiple sclerosis 62 Systemic lupus erythematosus SLE 62 systemic scleroderma 62 Hirschsprung Disease 62 CIDP 62 debilitating neurodegenerative 61 retinitis pigmentosa hereditary 61 Leber Congenital Amaurosis 61 pigmentosa 61 diffuse intrinsic pontine glioma 61 Chiari malformation 61 Hutchinson Gilford Progeria 61 neuroblastoma tumor 61 DIPG 61 Duchenne muscular dystrophy DMD 61 Mitochondrial diseases 61 muscle degeneration 61 Down syndrome chromosomal disorder 61 Hirschsprung disease 61 biliary atresia 61 rhabdomyosarcoma 61 Chronic lymphocytic leukemia 61 cystic fibrosis hereditary 61 Autoimmune disorders 61 Duchenne muscular dystrophy 61 spinal muscle atrophy 61 AAT deficiency 61 neurodevelopmental disorder 61 Mitochondrial disease 61 Fragile X Syndrome 61 neurobiological disorder 61 DiGeorge Syndrome 61 Pulmonary arterial hypertension 61 optic atrophy 61 Raynaud disease 61 spinal muscular atrophy 61 FTLD 61 syringomyelia 61 Tourette syndrome neurological disorder 61 Alport Syndrome 61 rheumatic disease 61 osteogenesis imperfecta 61 Leber hereditary optic neuropathy 61 Lou Gehrigs disease 61 histiocytosis 61 mental retardation cerebral palsy 61 genetic neuromuscular disorder 61 lymphoblastic lymphoma 61 fronto temporal dementia 61 ataxias 61 multisystem disease 61 motor neuron diseases 61 Shy Drager syndrome 61 chiari malformation 61 ataxia 61 Psoriatic arthritis 61 Severe Combined Immunodeficiency 61 autosomal recessive disorder 61 Hypoplastic Left Heart 61 Cockayne syndrome 61 osteogenic sarcoma 61 alveolar rhabdomyosarcoma 61 severely impairs 61 Diamond Blackfan anemia 61 Essential Tremor 61 Fanconi Anemia 61 pseudotumor cerebri 61 fatal myelination disorder 61 dystonia 61 hormonal disorder 61 neurological degeneration 61 Sandhoff disease 61 neurofibromatosis NF 61 NF1 61 fibrodysplasia ossificans progressiva FOP 61 frontal temporal dementia 61 Wilms tumor 61 Neurofibromatosis 61 nonalcoholic cirrhosis 61 Acute myeloid leukemia 61 Parkinson disease 60 Chronic Inflammatory Demyelinating Polyneuropathy 60 leukoencephalopathy 60 progressive degenerative neurological 60 AAT Deficiency 60 Spinal Muscular Atrophy SMA 60 Burkitt Lymphoma 60 adrenoleukodystrophy ALD 60 Aortic stenosis 60 Hashimoto thyroiditis 60 dystrophy 60 Acute Myelogenous Leukemia 60 familial ALS 60 osteopetrosis 60 disease Chronic Traumatic 60 idiopathic cardiomyopathy 60 Endometrial cancer 60 severe aplastic anemia 60 Arrhythmogenic Right Ventricular Cardiomyopathy 60 progressive supranuclear palsy 60 neurologic disorder 60 retinal degenerative disease 60 Osteogenesis Imperfecta 60 debilitating neurodegenerative disorder 60 arrhythmogenic right 60 muscular degeneration 60 myasthenia gravis 60 DiGeorge syndrome rare 60 multiforme 60 Churg Strauss syndrome 60 variable immunodeficiency 60 Morquio syndrome 60 degenerative brain 60 Tay Sachs disease 60 Kufs disease 60 autosomal dominant disorder 60 Meckel Gruber 60 congenital diaphragmatic hernia 60 Rhabdomyosarcoma rare 60 osteogenesis imperfecta OI 60 Anencephaly 60 Huntington Chorea 60 Idiopathic pulmonary fibrosis 60 Emphysema 60 recessive genetic 60 primary pulmonary hypertension 60 Von Hippel Lindau 60 Duchene muscular dystrophy 60 cerebal palsy 60 Parkinson Disease PD 60 stem glioma 60 genetic lysosomal storage 60 arthrogryposis multiplex congenita 60 progressive neurologic 60 Morquio Syndrome 60 Neuroblastoma 60 skeletal dysplasia 60 encephalitis swelling 60 Diabetic retinopathy 60 autosomal dominant 60 synovial sarcoma 60 Rheumatoid arthritis 60 spastic paralysis 60 leukoencephalopathy PML 60 rare autosomal recessive 60 Myelodysplastic syndrome 60 Alzheimers disease 60 disease 60 Myocarditis 60 tuberous sclerosis 60 galactosemia 59 chronic autoimmune 59 humans variant Creutzfeldt 59 retinal degeneration 59 myelodysplasia 59 cystic kidney 59 ventricular dysplasia 59 Parkinson disease neurodegenerative disorder 59 Hereditary angioedema 59 Ankylosing spondylitis 59 degenerative disorders 59 cardiomyopathy weakening 59 multisystem disorder 59 ARVD 59 Diamond Blackfan Anemia 59 Treacher Collins syndrome 59 PKU genetic 59 Rett syndrome neurological disorder 59 Cardiomyopathy 59 multi infarct dementia 59 Congestive heart failure 59 amyloidosis 59 neurocysticercosis 59 Ewings Sarcoma 59 polyneuropathy 59 retinoblastoma rare 59 Epstein Barr Virus 59 incurable degenerative brain 59 FSGS 59 Glioblastoma 59 myasthenia gravis MG 59 MELAS 59 disabling neurological condition 59 Friedreich Ataxia 59 systemic amyloidosis 59 Transverse Myelitis 59 Wegener granulomatosis 59 neuro degenerative 59 Moebius Syndrome 59 muscular dystrophy 59 truncus arteriosus 59 Juvenile Rheumatoid Arthritis 59 progeria rare 59 lysosomal storage disease 59 motor neurones 59 recessive dystrophic epidermolysis bullosa 59 autism neurological disorder 59 Pelizaeus Merzbacher disease 59 leukodystrophies 59 ceroid lipofuscinosis NCL 59 ataxia telangiectasia AT 59 Fanconi anemia rare 59 Neurofibromatosis Type 59 Progeria 59 Dilated cardiomyopathy 59 NPHP 59 nephritis 59 xeroderma pigmentosum 59 Non Hodgkins lymphoma 59 irreversible blindness 59 Peripheral neuropathy 59 Henoch purpura 59 neurological 59 carcinoid cancer 59 facioscapulohumeral muscular dystrophy 59 paralysis blindness 59 demyelinating disease 59 common disabling neurological 59 fibrous dysplasia 59 Acute Leukemia 59 Dystonia 59 retinitis 59 myelogenous leukemia 59 Holoprosencephaly 59 Hemolytic Uremic Syndrome HUS 59 Nephrogenic Systemic Fibrosis NSF 58 polycystic kidneys 58 nerve degeneration 58 developmental disorder 58 Alagille syndrome 58 autosomal recessive genetic 58 Ectopia Cordis 58 myelopathy 58 Rett Syndrome 58 Perthes disease 58 neurogenetic 58 Childhood Disorder 58 Tourette Syndrome TS 58 Guillain Barré Syndrome 58 Niemann Pick 58 polymyalgia 58 dystonia neurological disorder 58 amyotrophic lateral sclerosis 58 neurological ailment 58 incurable disease 58 diaphragmatic hernia 58 phenylketonuria 58 debilitating neuromuscular 58 Severe Primary IGFD 58 gastrointestinal stromal tumor 58 Pleural mesothelioma 58 congenital glaucoma 58 sacral agenesis 58 tricuspid atresia 58 chronic degenerative neurological 58 TTR amyloidosis 58 pontine glioma 58 spasmodic dysphonia 58 neurofibromatosis type 58 muscular dystrophy cystic fibrosis 58 genetically inherited 58 aplastic anemia 58 familial adenomatous polyposis 58 Malignant mesothelioma 58 multiple sclerosis 58 Burkitt lymphoma 58 cerebral palsy 58 Noonan Syndrome 58 neuro muscular disease 58 debilitating arthritis 58 frontotemporal dementia 58 Major depressive disorder 58 lymphocytic leukemia 58 Dravet Syndrome 58 Spinal Muscular Atrophy 58 autoimmune encephalitis 58 Fragile X syndrome 58 Wilms Tumour 58 infection progressive multifocal 58 Hyperthyroidism 58 Tourette Syndrome neurological disorder 58 congenital blindness 58 Sjogren Syndrome 58 thyroiditis 58 gene MECP2 58 Apert syndrome 58 prematurity ROP 58 angiosarcoma 58 polyneuropathy CIDP 58 cerebral palsy epilepsy 58 degenerative neurological diseases 58 Hemochromatosis 58 Rett syndrome 58 hemolytic anemia 58 Acute Myelogenous Leukemia AML 58 fungal meningitis 58 nonsense mutation 58 incurable degenerative disorder 58 Obsessive compulsive disorder 58 neurofibromatosis genetic disorder 58 1 diabetes T1D 58 Alport syndrome 58 combined immunodeficiency SCID 58 Spina bifida 58 systemic autoimmune 58 Cholangiocarcinoma 58 Erb palsy 58 Sjögren syndrome 58 hypotonia 58 primary lateral sclerosis 58 Sanfilippo syndrome 58 Battens Disease 58 respiratory insufficiency 58 Duchenne Muscular Dystrophy DMD 58 medium chain acyl 58 hypophosphatasia 58 lymphangioleiomyomatosis LAM 58 Combined Immune Deficiency 58 MCAD deficiency 58 Lewy Body dementia 58 Beta thalassemia 58 Acute Myeloid Leukaemia 58 Leber Hereditary Optic Neuropathy 58 neurological disorder characterized 58 Wilms Tumor 58 Creutzfeldt Jacob 58 wet macular degeneration 58 cerebellar hypoplasia 58 Lesch Nyhan syndrome 58 Polycystic ovary syndrome PCOS 58 aplastic anemia rare 58 Shwachman Diamond Syndrome 58 Benign Paroxysmal Positional Vertigo 58 progressive neurodegenerative disorders 57 cystic fibrosis Duchenne muscular 57 neuroblastoma 57 Charcot Marie Tooth 57 demyelinating disorders 57 Treacher Collins Syndrome 57 severe malignant osteopetrosis 57 Nephrotic Syndrome 57 incurable lung 57 retinal dystrophy 57 epilepsy 57 cerebri 57 lysosomal storage diseases 57 aciduria 57 Retinopathy 57 Synovial Sarcoma 57 respiratory gastrointestinal 57 Interstitial cystitis 57 ruptured brain aneurysm 57 dysautonomia 57 onset Alzheimer 57 aneuploidies 57 Tuberous sclerosis 57 inherited mutations 57 pernicious anemia 57 debilitating neurological 57 Cancer cachexia 57 Apert Syndrome 57 lymphoblastic leukemia 57 intractable epilepsy 57 diabetic kidney 57 cortical dysplasia 57 BH4 deficiency 57 Meniere Disease 57 ATTR PN 57 dysgenesis 57 Glioblastoma multiforme GBM 57 Pervasive Developmental Disorder 57 Glioma 57 myasthenia gravis neuromuscular 57 subarachnoid haemorrhage 57 hypothalamic hamartoma 57 aortic valve stenosis 57 Critical limb ischemia 57 hemochromatosis 57 diseases chronic granulomatous 57 incurable neurological disease 57 juvenile rheumatoid arthritis 57 Sporadic CJD 57 esophageal atresia 57 degenerative retinal disease 57 Marfan syndrome 57 tremors rigidity 57 Frontal lobe 57 RPE# 57 rhabdomyosarcoma rare cancer 57 eosinophilic esophagitis 57 genetic abnormality 57 primary sclerosing cholangitis 57 Wolf Hirschhorn 57 Focal dystonia 57 Friedrich Ataxia 57 Biliary atresia 57 Duchenne Muscular Dystrophy 57 VCFS 57 optic neuropathy 57 autoimmune hemolytic anemia 57 demyelination 57 Dysplasia 57 epilepsies 57 osteosarcoma bone 57 opsoclonus myoclonus syndrome 57 leiomyosarcoma rare 57 macular dystrophy 57 cystic fibrosis chronic pancreatitis 57 cardiac channelopathies 57 amyotrophic lateral sclerosis ALS 57 sclerosis ALS 57 underactive thyroid gland 57 ANCA associated 57 Lou Gehrig Disease 57 Moyamoya disease 57 Xeroderma Pigmentosum XP 57 dystonia neurological movement 57 Alzheimer Disease AD 57 progressive muscular atrophy 57 HGPS 57 Myopathy 57 Cockayne Syndrome 57 mitochondrial dysfunction 57 generalized epilepsy 57 myalgic encephalomyelitis 57 cardiac hypertrophy 57 primary ciliary dyskinesia 57 Obstructive sleep apnea 57 ependymoma 57 hypertrophic cardiomyopathy HCM 57 restrictive cardiomyopathy 57 Crigler Najjar syndrome 57 Arteriovenous Malformation 57 herpes encephalitis 57 Hypertrophic cardiomyopathy 57 severe obstructive pulmonary 57 Aortic dissection 57 biliary atresia rare 57 JMML 57 mastocytosis 57 Long QT syndrome 57 immunodeficiency 57 Crouzon syndrome 57 Parkinsonism 57 Neuropathic pain 57 Peritoneal mesothelioma 57 enterocolitis 57 hereditary hemorrhagic telangiectasia 56 Lennox Gastaut Syndrome 56 encephalitis meningitis 56 scleroderma chronic 56 autosomal recessive 56 neurobehavioral disorder 56 traumatic spinal cord 56 Creutzfeld Jakob disease 56 Ataxia 56 associated tremor ataxia 56 autoimmune 56 paralytic illness 56 onset Alzheimer disease 56 aortic rupture 56 gene mutation 56 degenerative neurological 56 degenerative bone 56 Wegener Granulomatosis 56 Osteogenesis imperfecta 56 Pericarditis 56 Insulin resistance 56 Porphyria 56 Li Fraumeni syndrome 56 monogenic 56 alzheimer disease 56 hemiparesis 56 mental retardation blindness 56 inherited retinal 56 hydrops 56 Bardet Biedl syndrome 56 Spinal cord injury 56 Chronic fatigue 56 optica 56 Moebius syndrome 56 lissencephaly 56 Systemic lupus erythematosus 56 Ulcerative colitis 56 scleroderma 56 inherited degenerative 56 autosomal recessive disease 56 Myasthenia 56 familial hypercholesterolemia 56 multiple sclerosis lupus 56 beta thalassemia 56 bicuspid valve 56 apraxia 56 Prader Willi syndrome 56 Male pattern baldness 56 Adrenoleukodystrophy 56 Iron deficiency anemia 56 mental retardation epilepsy 56 Peutz Jeghers syndrome 56 FMR1 gene 56 Long QT Syndrome 56 degenerative spinal 56 Enlarged prostate 56 motor neurone 56 autoimmune thyroid 56 Presbyopia 56 polymorphic ventricular tachycardia 56 Focal Segmental Glomerulosclerosis 56 auditory neuropathy 56 rheumatoid arthritis 56 neurodevelopment disorder 56 Congenital Muscular Dystrophy 56 juvenile myoclonic epilepsy 56 paraneoplastic 56 Variant CJD 56 dysphasia 56 congenital disorders 56 clotting disorder 56 Wilms tumors 56 nephrosis 56 polymyalgia rheumatica 56 Creutzfeldt Jakob disease 56 McCune Albright 56 Meningiomas 56 1 antitrypsin deficiency 56 progressive retinal degenerative 56 LHON 56 WAGR syndrome 56 Colorectal cancers 56 Migraine headache 56 Juvenile Idiopathic Arthritis JIA 56 bilateral retinoblastoma 56 epilepsy neurological disorder 56 Arthrogryposis 56 psychosocial dwarfism 56 spastic quadriplegia 56 Klippel Trenaunay Syndrome 56 alpha1 antitrypsin deficiency 56 seizure disorders 56 non hodgkins lymphoma 56 retinoblastoma cancerous tumor 56 unprovoked seizures 56 Spasmodic dysphonia 56 arthritis RA 56 Rheumatic fever 56 Lennox Gastaut syndrome 56 muscular dystrophy cerebral palsy 56 severe congenital neutropenia 56 Brugada syndrome 56 Atrial fibrillation AF 56 Ribavirin causes 56 heart syndrome HLHS 56 cystic fibrosis 56 Inflammatory Bowel 56 Cryptococcus neoformans 56 Parkinsonian Syndromes 56 myelomeningocele 56 torn flexor muscle 56 Eisenmenger syndrome 56 Sarcoidosis 56 Chiari Malformation 56 pulmonary thromboembolism 56 Wilm tumor 56 Langerhans Cell Histiocytosis 56 spinocerebellar ataxia type 56 genetic syndromes 56 neurofibromas 56 Fibrosis 56 Periodontal disease 56 prosopagnosia 56 Sturge Weber syndrome 56 Kawasaki Disease 56 Rhabdomyolysis 56 complement inhibitor eculizumab 56 Cerebral malaria 56 immuno deficiency 56 Irritable bowel syndrome IBS 56 disorder thalassemia 56 Generalized anxiety disorder 56 congenital anomaly 56 adenoid cystic carcinoma 56 neuropathic pain spasticity 56 complex neurobiological disorder 56 congenital deafness 56 Sjogren syndrome 56 Cystinosis 56 incurable lung cancer 56 Epstein Barr virus EBV 56 Infant botulism 56 spinal meningitis 56 tics involuntary 56 interstitial pulmonary fibrosis 56 Follicular lymphoma 56 thoracic aortic aneurysm 56 bladder exstrophy 56 Morquio 56 congenital hydrocephalus 56 glomerulonephritis 56 vasculitis 56 Alopecia Areata 56 neuritis 55 Fanconi Anaemia 55 endocrine disorder 55 diabetes insipidus 55 Glioblastoma Multiforme 55 Spasticity 55 macular disease 55 idiopathic PAH 55 Hemiplegia 55 Atopic eczema 55 Von Willebrand 55 metabolic abnormality 55 Hodgkins Lymphoma 55 von Hippel Lindau 55 myopathies 55 idiopathic dilated cardiomyopathy 55 neurofibroma 55 Sarcopenia 55 leptin deficiency 55 hemiplegia 55 myotonic muscular dystrophy 55 Ataxia Telangiectasia 55 mitochondrial diseases 55 roseola 55 cerebral vascular disease 55 Parkinson disease PD 55 chronic rheumatic 55 anosognosia 55 Stargardt macular dystrophy 55 chronic progressive neurodegenerative 55 disorder Creutzfeldt Jakob 55 developmental abnormalities 55 Parkinson Disease 55 profound deafness 55 Osteoarthritis OA 55 Beckwith Wiedemann syndrome 55 transfusion syndrome 55 carcinoid 55 FXTAS 55 Behcet syndrome 55 smoldering myeloma 55 AML Leukemia 55 PCNSL 55 channelopathies 55 erythematosus 55 focal dystonia 55 motor neuron degeneration 55 Acute Lymphoblastic Leukemia 55 cardio myopathy 55 Magnesium deficiency 55 hereditary deafness 55 tremors slowness 55 velo cardio facial 55 toxemia 55 moyamoya 55 polydactylism 55 autoinflammatory diseases 55 Gastroparesis 55 inherited genetic mutation 55 facial palsy 55 congenital cataract 55 Hodgkin Disease 55 Epidermolysis bullosa 55 thrombotic thrombocytopenic purpura 55 Creutzfeldt Jakob 55 Eloysa Vasquez 55 Wet AMD 55 diffuse pontine glioma 55 muscle rigidity 55 scoliosis 55 Obstetric fistula 55 Prion diseases 55 cortical blindness 55 pulmonary stenosis 55 petit mal seizures 55 Chronic sinusitis 55 myelodysplastic syndrome 55 hematologic disorders 55 sporadic Creutzfeldt Jakob 55 disorders infectious diseases 55 Hemolytic Uremic Syndrome 55 spastic quadriplegic cerebral palsy 55 Dwarfism 55 acute myeloid leukemia 55 Cystic Fibrosis CF 55 incurable illness 55 myotonia 55 aniridia 55 cardiomyopathy 55 blindness deafness 55 peritoneal mesothelioma 55 degenerative motor neuron 55 opportunistic viral infection 55 intestinal inflammation 55 Keratoconus 55 debilitating migraine headaches 55 cerebral thrombosis 55 Histiocytosis 55 paresis 55 frontal lobe dementia 55 Genital herpes 55 neurosyphilis 55 acromegaly 55 Degenerative disc disease 55 familial dysautonomia 55 Lupus nephritis 55 Scleroderma 55 acute myocarditis 55 Parkinson disease multiple sclerosis 55 de novo mutations 55 Congenital Adrenal Hyperplasia 55 Diabetic nephropathy 55 myeloproliferative neoplasms 55 disease focal segmental 55 Congenital heart 55 acute myelogenous leukemia AML 55 Cushing syndrome 55 Dystrophin 55 Aspergers Syndrome 55 Mitochondrial 55 Reflex Sympathetic Dystrophy Syndrome 55 cystic fibrosis CF 55 Treacher Collins 55 prion disease 55 Myalgic Encephalomyelitis 55 leukemia 55 Tay Sachs thalassemia 55 Peripheral artery disease 55 ventricular cardiomyopathy 55 Malignant gliomas 55 Vitamin B# deficiency 55 congenital kidney 55 Avascular necrosis 55 aphasia 55 congenital abnormality 55 Variant Creutzfeldt Jakob Disease 55 ALS amyotrophic lateral sclerosis 55 genetic defects 55 Lewy Body Dementia 55 neurological diseases 55 chromosomal abnormality 55 Langerhans cell histiocytosis 55 situs inversus 55 dermatologic reactions 55 neurological manifestations 55 CdLS 55 Pervasive Developmental Disorders 55 limb girdle muscular dystrophy 55 neurologic deficits 55 Eosinophilic 55 bone deformities 55 muscle spasticity 55 arteriovenous malformation AVM 55 Ectodermal Dysplasia 55 polyomavirus nephropathy 55 primitive neuroectodermal tumors 55 choriocarcinoma 55 FSHD 55 congenital cataracts 55 viral cardiomyopathy 55 debilitating affliction 55 Alzheimer disease 55 systemic mastocytosis 55 nephrotic syndrome 55 G#S mutation 55 Multiple sclerosis affects 55 valvular heart disease 55 neuronal degeneration 55 juvenile diabetes 55 LQTS 55 congenital deficiency 55 arterial fibrillation 55 temporomandibular joint disorder 55 Oxidative stress 55 infantile spasms 54 nonhereditary 54 immunodeficiencies 54 Cytomegalovirus 54 Mucositis 54 Genetic mutation 54 congenital adrenal hyperplasia CAH 54 sporadic ALS 54 progressive multifocal PML 54 Alzheimer disease AD 54 vWD 54 genetic mutation 54 interrupted aortic arch