myotonic dystrophy

Related by string. Myotonic dystrophy * Myotonic : myotonic muscular dystrophy . Myotonic Muscular Dystrophy . myotonic . Myotonic Dystrophy / Dystrophy : cerebral palsy muscular dystrophy . Duchenne muscular dystrophy DMD . Duchenne Muscular Dystrophy DMD . Muscular Dystrophy PPMD . reflex sympathetic dystrophy . Muscular Dystrophy Telethon . Duchenne muscular dystrophy * *

Related by context. Frequent words. (Click for all words.) 69 mitochondrial dysfunction 69 neurodegenerative disorder 68 degenerative disorder 65 Friedreich ataxia 65 Fanconi anemia 63 nonsense mutation 63 genetic defect 63 genetic disorder 63 Wnt signaling 62 NF1 62 retinal degeneration 62 metabolic disorder 61 enzyme deficiency 61 Rett syndrome 61 neurodegenerative disease 61 genetic abnormality 61 mitochondrial disease 61 mutated gene 61 hereditary disorder 61 motor neuron disease 61 dilated cardiomyopathy 60 LQTS 60 long QT syndrome 60 infantile spasms 60 dystrophin 60 SOD1 60 progressive degeneration 60 mutant protein 60 neurodegeneration 60 dystrophy 59 fatal neurodegenerative 59 beta thalassemia 59 epilepsy 59 myelination 59 Fragile X Syndrome 59 cellular pathways 59 Cushing syndrome 59 p# gene 59 Long QT Syndrome 58 immunodeficiency 58 demyelination 58 FSGS 58 osteogenesis imperfecta 58 hemolytic anemia 58 Alzheimers disease 58 alpha synuclein 58 behavioral abnormalities 58 rhabdomyosarcoma 58 primary pulmonary hypertension 58 Duchenne muscular dystrophy 58 Fragile X syndrome 57 genetic alteration 57 primary biliary cirrhosis 57 Rett Syndrome 57 neurological dysfunction 57 tau protein 57 intestinal inflammation 57 frontotemporal dementia 57 defective gene 57 progressive degenerative 57 cholesterol metabolism 57 myasthenia gravis 57 amyloids 57 amyloidosis 57 medulloblastoma 57 phenylketonuria 57 prion disease 57 dystonia 57 neuropsychiatric disorders 57 Insulin resistance 57 Wilms tumor 57 dysregulation 56 acute myelogenous leukemia AML 56 autoimmunity 56 Mitochondrial 56 neuroendocrine 56 susceptibility gene 56 FSHD 56 gene mutation 56 neurofibromatosis 56 hemochromatosis 56 chronic myeloid leukemia CML 56 neurotransmission 56 genetic abnormalities 56 Prader Willi syndrome 56 neurogenic 56 biliary atresia 56 genetic mutation 56 Progeria 56 tumor suppressor genes 56 cardiac dysfunction 56 metabolic abnormalities 56 parkinsonism 56 biochemical pathway 56 urea cycle 56 cardiac abnormalities 55 Gaucher disease 55 PrP 55 TGF beta 55 mutation 55 misfolding

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