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 Categorias DeCS

C06 Digestive System Diseases .
C06.552 Liver Diseases .
C06.552.241 Fatty Liver .
C06.552.241.649 Reye Syndrome .
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 .
C10.228.140.163.100.813 Refsum Disease .
C10.228.140.163.780 Reye Syndrome .
C10.228.140.430 Encephalitis .
C10.500 Nervous System Malformations .
C10.500.300 Hereditary Sensory and Motor Neuropathy .
C10.500.300.780 Refsum Disease .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.495 Hereditary Sensory and Motor Neuropathy .
C10.574.500.495.780 Refsum Disease .
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 .
C10.668 Neuromuscular Diseases .
C10.668.829 Peripheral Nervous System Diseases .
C10.668.829.800 Polyneuropathies .
C10.668.829.800.300 Hereditary Sensory and Motor Neuropathy .
C10.668.829.800.300.780 Refsum Disease .
C12 Male Urogenital Diseases .
C12.777 Urologic Diseases .
C12.777.419 Kidney Diseases .
C12.777.419.936 Uremia .
C12.777.419.936.463 Hemolytic-Uremic Syndrome .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.968 Urologic Diseases .
C13.351.968.419 Kidney Diseases .
C13.351.968.419.936 Uremia .
C13.351.968.419.936.463 Hemolytic-Uremic Syndrome .
C15 Hemic and Lymphatic Diseases .
C15.378 Hematologic Diseases .
C15.378.071 Anemia .
C15.378.071.141 Anemia, Hemolytic .
C15.378.071.141.610 Hemolytic-Uremic Syndrome .
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 .
C15.378.140 Blood Platelet Disorders .
C15.378.140.855 Thrombocytopenia .
C15.378.140.855.925 Thrombotic Microangiopathies .
C15.378.140.855.925.500 Hemolytic-Uremic Syndrome .
C15.378.463 Hemorrhagic Disorders .
C15.378.463.325 Factor XI Deficiency .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.666 Nervous System Malformations .
C16.131.666.300 Hereditary Sensory and Motor Neuropathy .
C16.131.666.300.780 Refsum Disease .
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 .
C16.320.400.375 Hereditary Sensory and Motor Neuropathy .
C16.320.400.375.780 Refsum Disease .
C16.320.400.525 Mental Retardation, X-Linked .
C16.320.400.525.937 Rett Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.813 Refsum Disease .
C16.320.565.663 Peroxisomal Disorders .
C16.320.565.663.760 Refsum Disease .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.813 Refsum Disease .
C18.452.132.780 Reye Syndrome .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.813 Refsum Disease .
C18.452.648.663 Peroxisomal Disorders .
C18.452.648.663.760 Refsum Disease .
C19 Endocrine System Diseases .
C19.053 Adrenal Gland Diseases .
C19.053.800 Adrenocortical Hyperfunction .
C19.053.800.604 Hyperaldosteronism .
 
 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
 
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 .
0.62
 
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 .
0.59
 
Reye Syndrome .
Fatty Liver with Encephalopathy .
Reye Syndrome, Adult .
Reye's Syndrome .
Reye's Syndrome, Adult .
Reye's-Like Syndrome .
Reye-Johnson Syndrome .
Reye-Like Syndrome .
Adult Reye Syndrome .
Adult Reye's Syndrome .
Reye Johnson Syndrome .
Reye Like Syndrome .
Reye's Like Syndrome .
0.57
 
Hemolytic-Uremic Syndrome .
Gasser Syndrome .
Gassers Syndrome .
Hemolytic Uremic Syndrome .
Syndrome, Hemolytic-Uremic .
Gasser's Syndrome .
0.57
 
Hyperaldosteronism .
Conn Syndrome .
Conn's Syndrome .
Primary Hyperaldosteronism .
Conns Syndrome .
Hyperaldosteronism, Primary .
Syndrome, Conn .
Syndrome, Conn's .
Aldosteronism .
0.57
 
Refsum Disease .
Adult Refsum Disease .
Classic Refsum Disease .
HMSN 4 .
HMSN IV .
Hemeralopia Heredoataxia Polyneuritiformis .
Hereditary Motor And Sensory Neuropathy IV .
Hereditary Motor and Sensory Neuropathy Type IV .
Hereditary Motor and Sensory Neuropathy, Type IV .
Hereditary Type IV Motor and Sensory Neuropathy .
Phytanic Acid Oxidase Deficiency .
Refsum Disease, Adult .
Refsum Disease, Classic .
Refsum Disease, Phytanic Acid Oxidase Deficiency .
Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency .
Refsum Syndrome .
Refsum's Disease .
Refsum's Syndrome .
Refsum-Thiebaut Syndrome .
Adult Refsum Diseases .
Classic Refsum Diseases .
Disease, Adult Refsum .
Disease, Classic Refsum .
Disease, Refsum .
Disease, Refsum's .
Diseases, Adult Refsum .
Diseases, Classic Refsum .
HMSN IVs .
Heredoataxia Polyneuritiformis, Hemeralopia .
Polyneuritiformis, Hemeralopia Heredoataxia .
Polyneuritiformis, Heredopathia Atactica .
Refsum Disease, Phytanoyl CoA Hydroxylase Deficiency .
Refsum Diseases, Adult .
Refsum Diseases, Classic .
Refsum Thiebaut Syndrome .
Refsum-Thiebaut Syndromes .
Refsums Disease .
Refsums Syndrome .
Syndrome, Refsum .
Syndrome, Refsum's .
Syndrome, Refsum-Thiebaut .
Syndromes, Refsum-Thiebaut .
Heredopathia Atactica Polyneuritiformis .
HMSN Type IV .
Neuropathy, Hereditary Motor and Sensory, Type IV .
Phytanic Acid Storage Disease .
Hereditary-Motor and Sensory-Neuropathy Type IV .
HEREDITARY-MOTOR AND SENSORY NEUROPATHY TYPE IV .
HEREDITARY TYPE IV MOTOR AND SENSORY NEUROPATHY .
NEUROPATHY, HEREDITARY MOTOR AND SENSORY TYPE IV .
REFSUM'S SYNDROME .
REFSUM'S DISEASE .
0.56