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 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 .
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 .
C14 Cardiovascular Diseases .
C14.907 Vascular Diseases .
C14.907.454 Hemostatic Disorders .
C14.907.454.900 Telangiectasia, Hereditary Hemorrhagic .
C14.907.823 Telangiectasis .
C14.907.823.780 Telangiectasia, Hereditary Hemorrhagic .
C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.100 Blood Coagulation Disorders .
C15.378.100.100 Blood Coagulation Disorders, Inherited .
C15.378.100.100.300 Factor V Deficiency .
C15.378.100.141 Coagulation Protein Disorders .
C15.378.100.141.300 Factor V Deficiency .
C15.378.463 Hemorrhagic Disorders .
C15.378.463.300 Factor V Deficiency .
C15.378.463.515 Hemostatic Disorders .
C15.378.463.515.900 Telangiectasia, Hereditary Hemorrhagic .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.240 Cardiovascular Abnormalities .
C16.131.240.850 Vascular Malformations .
C16.131.240.850.968 Telangiectasia, Hereditary Hemorrhagic .
C16.320 Genetic Diseases, Inborn .
C16.320.099 Blood Coagulation Disorders, Inherited .
C16.320.099.300 Factor V Deficiency .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.100 Dent Disease .
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 .
C16.320.565.861 Renal Tubular Transport, Inborn Errors .
C16.320.565.861.271 Dent Disease .
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 .
C18.452.648.861 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 .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.355 Fibrosis .
C23.550.355.700 Retroperitoneal Fibrosis .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Factor V Deficiency .
Deficiency, Factor 5 .
Deficiency, Factor Five .
Deficiency, Factor V .
Factor 5 Deficiency .
Factor Five Deficiency .
Labile Factor Deficiency .
Owren Parahemophilia .
Owren's Disease .
Deficiencies, Factor 5 .
Deficiencies, Factor Five .
Deficiencies, Factor V .
Deficiencies, Labile Factor .
Deficiency, Labile Factor .
Disease, Owren .
Disease, Owren's .
Factor 5 Deficiencies .
Factor Five Deficiencies .
Factor V Deficiencies .
Labile Factor Deficiencies .
Owrens Disease .
Parahemophilia, Owren .
Parahemophilias .
Owren Disease .
Parahemophilia .
1.00
 
Dent Disease .
Dents Disease .
Disease, Dent .
Disease, Dent's .
Disease, Dents .
Dent's Disease .
0.56
 
Telangiectasia, Hereditary Hemorrhagic .
Hereditary Hemorrhagic Telangiectasia .
Osler's Disease .
Osler-Rendu-Weber Disease .
Osler-Weber-Rendu Syndrome .
Rendu-Osler-Weber .
Telangiectasia, Hereditary Hemorrhagic, Type 1 .
Telangiectasia, Hereditary Hemorrhagic, of Rendu, Osler, and Weber .
Weber-Osler .
Disease, Osler's .
Hemorrhagic Telangiectasia, Hereditary .
Osler Disease .
Osler Rendu Disease .
Osler Rendu Weber Disease .
Osler Weber Rendu Syndrome .
Rendu Osler Weber .
Weber Osler .
Osler-Rendu Disease .
0.56
 
Retroperitoneal Fibrosis .
Fibrosis, Inflammatory Perianeurysmal .
Fibrosis, Perianeurysmal Inflammatory .
Idiopathic Retroperitoneal Fibrosis .
Inflammatory Fibrosis, Perianeurysmal .
Inflammatory Perianeurysmal Fibrosis .
Ormond's Disease .
Perianeurysmal Inflammatory Fibrosis .
Chronic Periaortitides .
Chronic Periaortitis .
Disease, Ormond .
Disease, Ormond's .
Fibroses, Retroperitoneal .
Fibrosis, Retroperitoneal .
Periaortitides, Chronic .
Retroperitoneal Fibroses .
Ormond Disease .
Perianeurysmal Fibrosis, Inflammatory .
Periaortitis, Chronic .
0.55
 
Adrenocortical Adenoma .
Adenoma, Adrenocortical .
Conn Adenoma .
Conn Disease .
Adenoma, Conn .
Adenomas, Adrenal Cortical .
Adenomas, Adrenocortical .
Adenomas, Conn .
Adrenal Cortical Adenoma .
Adrenal Cortical Adenomas .
Adrenocortical Adenomas .
Conn Adenomas .
Conns Disease .
Disease, Conn .
Disease, Conn's .
Adenoma, Adrenal Cortical .
Conn's Disease .
0.55
 
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 .
0.55