Categorias DeCS
C04 Neoplasms .
C04.588 Neoplasms by Site .
C04.588.322 Endocrine Gland Neoplasms .
C04.588.322.078 Adrenal Gland Neoplasms .
C04.588.322.078.265 Adrenal Cortex Neoplasms .
C04.588.322.078.265.500 Adrenocortical Adenoma .
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 .
C16.320.565.202.449.520 Glycogen Storage Disease Type III .
C16.320.565.202.449.600 Glycogen Storage Disease Type VII .
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 .
C18.452.648.202.449.520 Glycogen Storage Disease Type III .
C18.452.648.202.449.600 Glycogen Storage Disease Type VII .
C18.452.648.861 Renal Tubular Transport, Inborn Errors .
C18.452.648.861.271 Dent Disease .
C19 Endocrine System Diseases .
C19.053 Adrenal Gland Diseases .
C19.053.098 Adrenal Cortex Diseases .
C19.053.098.265 Adrenal Cortex Neoplasms .
C19.053.098.265.500 Adrenocortical Adenoma .
C19.053.347 Adrenal Gland Neoplasms .
C19.053.347.500 Adrenal Cortex Neoplasms .
C19.053.347.500.500 Adrenocortical Adenoma .
C19.344 Endocrine Gland Neoplasms .
C19.344.078 Adrenal Gland Neoplasms .
C19.344.078.265 Adrenal Cortex Neoplasms .
C19.344.078.265.500 Adrenocortical Adenoma .
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| | Termos Sinônimos e Históricos | Documentos LILACS e MDL | | | | | | | | | | |
| Glycogen Storage Disease Type III . Amylo-1,6-Glucosidase Deficiency . Cori Disease . Deficiency, Debrancher . Glycogen Debrancher Deficiency . Glycogen Storage Disease III . Glycogen Storage Disease Type 3 . Amylo 1,6 Glucosidase Deficiency . Amylo-1,6-Glucosidase Deficiencies . Coris Disease . Debrancher Deficiencies . Debrancher Deficiencies, Glycogen . Debrancher Deficiency, Glycogen . Deficiencies, Amylo-1,6-Glucosidase . Deficiencies, Debrancher . Deficiencies, Glycogen Debrancher . Deficiency, Amylo-1,6-Glucosidase . Deficiency, Glycogen Debrancher . Dextrinoses, Limit . Dextrinosis, Limit . Disease, Cori . Disease, Cori's . Disease, Forbes . Glycogen Debrancher Deficiencies . Glycogenosis 3s . Limit Dextrinoses . Cori's Disease . Debrancher Deficiency . Forbes Disease . Glycogen Debranching Enzyme Deficiency . Glycogenosis 3 . Limit Dextrinosis . 0.60
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| 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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