serw-MX  [xml]  
 


    
 Categorias DeCS

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.430 Encephalitis .
C10.597 Neurologic Manifestations .
C10.597.606 Neurobehavioral Manifestations .
C10.597.606.643 Intellectual Disability .
C10.597.606.643.455 Mental Retardation, X-Linked .
C10.597.606.643.455.937 Rett Syndrome .
C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.100 Blood Coagulation Disorders .
C15.378.100.100 Blood Coagulation Disorders, Inherited .
C15.378.100.100.325 Factor XI Deficiency .
C15.378.100.141 Coagulation Protein Disorders .
C15.378.100.141.325 Factor XI Deficiency .
C15.378.463 Hemorrhagic Disorders .
C15.378.463.325 Factor XI Deficiency .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.099 Blood Coagulation Disorders, Inherited .
C16.320.099.325 Factor XI Deficiency .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.500 Mental Retardation, X-Linked .
C16.320.322.500.937 Rett Syndrome .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.525 Mental Retardation, X-Linked .
C16.320.400.525.937 Rett Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.300 Hyperbilirubinemia, Hereditary .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.300 Hyperbilirubinemia, Hereditary .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
C23.550.288.500 Syndrome .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Encephalitis .
Brain Inflammation .
Encephalitis, Rasmussen .
Rasmussen Encephalitis .
Rasmussen's Syndrome .
Brain Inflammations .
Inflammation, Brain .
Rasmussen Syndrome .
1.00
 
Syndrome .
Symptom Cluster .
Cluster, Symptom .
Clusters, Symptom .
Symptom Clusters .
Syndromes .
0.58
 
Rett Syndrome .
Autism, Dementia, Ataxia, and Loss of Purposeful Hand Use .
Rett Disorder .
Rett's Disorder .
Rett's Syndrome .
Autism Dementia Ataxia Loss of Purposeful Hand Use Syndrome .
Cerebroatrophic Hyperammonemias .
Hyperammonemia, Cerebroatrophic .
Hyperammonemias, Cerebroatrophic .
Retts Syndrome .
Syndrome, Rett .
Syndrome, Rett's .
Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome .
Cerebroatrophic Hyperammonemia .
0.51
 
Hyperbilirubinemia, Hereditary .
Hyperbilirubinemia, Rotor Type .
Hereditary Hyperbilirubinemia .
Hereditary Hyperbilirubinemias .
Hyperbilirubinemias, Hereditary .
Rotor Type Hyperbilirubinemia .
Syndrome, Rotor .
Rotor Syndrome .
0.49
 
Factor XI Deficiency .
Deficiency, Factor 11 .
Deficiency, Factor Eleven .
Deficiency, Factor XI .
Factor 11 Deficiency .
Factor Eleven Deficiency .
Plasma Thromboplastin Antecedent Deficiency .
Rosenthal's Syndrome .
Deficiencies, Factor 11 .
Deficiencies, Factor Eleven .
Deficiencies, Factor XI .
Factor 11 Deficiencies .
Factor Eleven Deficiencies .
Factor XI Deficiencies .
Rosenthal Syndromes .
Rosenthal's Syndromes .
Rosenthals Syndrome .
Syndrome, Rosenthal .
Syndrome, Rosenthal's .
Hemophilia C .
Rosenthal Syndrome .
PTA Deficiency .
0.48