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 Categorias DeCS

C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.540 Hyperostosis .
C05.116.540.410 Hyperostosis, Diffuse Idiopathic Skeletal .
C05.116.900 Spinal Diseases .
C05.116.900.815 Spinal Osteophytosis .
C05.116.900.815.651 Hyperostosis, Diffuse Idiopathic Skeletal .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.228.140.163.100.435.825 Sphingolipidoses .
C10.228.140.163.100.435.825.250 Farber Lipogranulomatosis .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.189.435.825 Sphingolipidoses .
C16.320.565.189.435.825.250 Farber Lipogranulomatosis .
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 .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.803 Sphingolipidoses .
C16.320.565.398.641.803.325 Farber Lipogranulomatosis .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.825 Sphingolipidoses .
C16.320.565.595.554.825.250 Farber Lipogranulomatosis .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.946 Sweat Gland Diseases .
C17.800.946.492 Miliaria .
C17.800.946.492.285 Fox-Fordyce Disease .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.132.100.435.825 Sphingolipidoses .
C18.452.132.100.435.825.250 Farber Lipogranulomatosis .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.325 Farber Lipogranulomatosis .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.825 Sphingolipidoses .
C18.452.648.189.435.825.250 Farber Lipogranulomatosis .
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 .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.803 Sphingolipidoses .
C18.452.648.398.641.803.325 Farber Lipogranulomatosis .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.825 Sphingolipidoses .
C18.452.648.595.554.825.250 Farber Lipogranulomatosis .
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 .
 
 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 .
1.00
 
Hyperostosis, Diffuse Idiopathic Skeletal .
Ankylosing Vertebral Hyperostosis with Tylosis .
Forestier's Disease .
Forestier-Rotes Disease .
Ankylosing Hyperostoses, Vertebral .
Ankylosing Hyperostosis, Vertebral .
Disease, Forestier .
Disease, Forestier's .
Disease, Forestier-Rotes .
Forestier Rotes Disease .
Forestiers Disease .
Hyperostoses, Vertebral Ankylosing .
Hyperostosis, Vertebral Ankylosing .
Vertebral Ankylosing Hyperostoses .
Forestier Disease .
Vertebral Ankylosing Hyperostosis .
Diffuse Idiopathic Skeletal Hyperostosis .
0.69
 
Disease .
Diseases .
Illness .
Disease Concept Evolution .
0.61
 
Fox-Fordyce Disease .
Fox-Fordyce Syndrome .
Apocrine Miliaria .
Disease, Fox-Fordyce .
Fox Fordyce Disease .
Fox Fordyce Syndrome .
Syndrome, Fox-Fordyce .
Miliaria, Apocrine .
0.58
 
Farber Lipogranulomatosis .
Acid Ceramidase Deficiency .
Ceramidase Deficiency .
Farber Disease .
Farber's Disease .
N-Laurylsphingosine Deacylase Deficiency .
Acid Ceramidase Deficiencies .
Ceramidase Deficiencies .
Ceramidase Deficiency, Acid .
Deficiencies, Ceramidase .
Deficiencies, N-Laurylsphingosine Deacylase .
Deficiency, Acid Ceramidase .
Deficiency, Ceramidase .
Deficiency, N-Laurylsphingosine Deacylase .
Disease, Farber's .
Diseases, Farber's .
Farber's Diseases .
Farbers Disease .
Lipogranulomatosis, Farber .
N Laurylsphingosine Deacylase Deficiency .
N-Laurylsphingosine Deacylase Deficiencies .
0.57