Categorias DeCS
C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.534 Muscular Disorders, Atrophic .
C05.651.534.500 Muscular Dystrophies .
C05.651.534.500.149 Glycogen Storage Disease Type VII .
C05.651.662 Myotonic Disorders .
C05.651.662.500 Myotonia Congenita .
C10 Nervous System Diseases .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.545 Myotonia Congenita .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.175 Muscular Disorders, Atrophic .
C10.668.491.175.500 Muscular Dystrophies .
C10.668.491.175.500.112 Glycogen Storage Disease Type VII .
C10.668.491.606 Myotonic Disorders .
C10.668.491.606.500 Myotonia Congenita .
C12 Male Urogenital Diseases .
C12.777 Urologic Diseases .
C12.777.419 Kidney Diseases .
C12.777.419.815 Renal Tubular Transport, Inborn Errors .
C12.777.419.815.364 Dent Disease .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.968 Urologic Diseases .
C13.351.968.419 Kidney Diseases .
C13.351.968.419.815 Renal Tubular Transport, Inborn Errors .
C13.351.968.419.815.364 Dent Disease .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.100 Dent Disease .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.540 Myotonia Congenita .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.449 Glycogen Storage Disease .
C16.320.565.202.449.600 Glycogen Storage Disease Type VII .
C16.320.565.663 Peroxisomal Disorders .
C16.320.565.663.050 Acatalasia .
C16.320.565.861 Renal Tubular Transport, Inborn Errors .
C16.320.565.861.271 Dent Disease .
C16.320.577 Muscular Dystrophies .
C16.320.577.149 Glycogen Storage Disease Type VII .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.449 Glycogen Storage Disease .
C18.452.648.202.449.600 Glycogen Storage Disease Type VII .
C18.452.648.663 Peroxisomal Disorders .
C18.452.648.663.050 Acatalasia .
C18.452.648.861 Renal Tubular Transport, Inborn Errors .
C18.452.648.861.271 Dent Disease .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
HP1 Homeopathy .
HP1.007 Homeopathic Philosophy .
HP1.007.262 Patients .
HP1.007.262.808 Disease .
HP2 Homeopathic Clinics .
HP2.029 Disease .
SP5 Epidemiology and Biostatistics .
SP5.001 Epidemiology .
SP5.001.002 Health-Disease Process .
SP5.001.002.013 Disease .
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| | Termos Sinônimos e Históricos | Documentos LILACS e MDL | | | | |
| Myotonia Congenita . Batten Turner Congenital Myopathy . Batten-Turner Congenital Myopathy . Becker Disease . Congenital Myotonia . Generalized Myotonia of Becker . Generalized Myotonia of Thomsen . Myopathy, Congenital . Myotonia Congenita, Autosomal Dominant . Myotonia Congenita, Autosomal Recessive . Myotonia Levior . Myotonia, Generalized . Thomsen's Disease . Thomsens Disease . Disease, Becker . Disease, Thomsen . Disease, Thomsen's . Disease, Thomsens . Generalized Myotonia . Generalized Myotonia, Becker . Generalized Myotonias . Myotonia, Becker Generalized . Myotonias, Generalized . Thomsen Generalized Myotonia . Thomsen Disease . Becker Generalized Myotonia . Myotonia, Generalized, Becker . THOMSEN'S DISEASE . 0.58
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