Related by context. Frequent words. (Click for all words.) 65 degenerative disorder 63 hereditary disorder 62 neurodegenerative disorder 62 genetic disorder 62 Friedreich ataxia 62 Fragile X Syndrome 60 fatal neurodegenerative 60 progressive degenerative 60 Ataxia 59 Rett syndrome 59 Fanconi anemia 59 neurofibromatosis 58 neuromuscular disease 58 FSGS 58 Duchenne muscular dystrophy DMD 58 dystrophy 58 Cystic fibrosis 58 genetic abnormality 58 Progeria 58 tuberous sclerosis 57 ataxia 56 neurological disorder 56 Rett Syndrome 56 NF1 56 genetic defect 56 enzyme deficiency 56 progressive neurodegenerative disease 56 rare neurological disorder 55 Dystonia 55 metabolic disorder 55 susceptibility gene 55 genetically inherited 55 hemolytic anemia 55 mitochondrial disease 55 Fragile X syndrome 55 nonsense mutation 55 biliary atresia 55 Neurofibromatosis 54 Prader Willi syndrome 54 Alzheimers disease 54 cystic fibrosis CF 54 neurodegenerative disease 54 motor neuron disease 54 Mitochondrial 54 frontotemporal dementia 54 mitochondrial dysfunction 54 mutant genes 54 HLH 53 long QT syndrome 53 Charcot Marie Tooth 53 Friedreich Ataxia 53 cystic fibrosis 53 herpes viruses 53 neuromuscular disorder 53 mutations 53 congenital disorder 53 muscular dystrophy 53 mitochondrial diseases 53 DISEASE 53 Burkitt lymphoma 53 myasthenia gravis 52 Osteosarcoma 52 osteogenesis imperfecta 52 Long QT Syndrome 52 Glioblastoma 52 hemochromatosis 52 Spinal Muscular Atrophy 52 primary immunodeficiency 52 rhabdomyosarcoma 52 susceptibility genes 52 Fragile X 52 Tay Sachs 52 immunodeficiency 52 cytomegalovirus CMV 52 progressive degeneration 52 mutated gene 52 spinal muscular atrophy 52 Cardiomyopathy 52 Spina bifida 52 ALS amyotrophic lateral sclerosis 52 polycystic ovary syndrome 52 gene mutation 52 syndromes 51 retinal degeneration 51 LRRK2 51 neurodevelopmental disorders 51 Wilms tumor 51 Batten Disease 51 Parkinsonism 51 acute myelogenous leukemia AML 51 genetic mutations 51 dilated cardiomyopathy 51 Marfan syndrome 51 SYMPTOMS 51 genetic disorders 51 Scleroderma 51 chromosomal abnormality 51 AUTISM 51 mutant gene 51 genetic defects 51 chronic autoimmune